Team:TU-Munich/Notebook/Labjournal

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Week 1 22.4-28.4
Week 2 29.4-05.5
Week 3 06.5-12.5
Week 4 13.5-19.5
Week 5 20.5-26.5
Week 6 27.5-02.6
Week 7 03.6-09.6
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Labjournal

Week 1

Monday, April 22nd

Transformation of E. coli XL1 blue with Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3)

Investigator: Jeff, Leonie, Rosario

Aim of the experiment: Transformation of Phytochrome B for protein fusion.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 2 µl of DNA was added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

Miniprep of pTUM100 with pGAL, pTEF1, pTEF2, pADH and RFC25 compatible RFP generator

Investigator: Jeff, Leonie, Rosario

Aim of the experiment: Miniprep of pTUM100 with pGAL, pTEF1, pTEF2, pADH and RFC25 compatible RFP generator

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)

Sequencing of RFP-Generator (RFC25, pSB1C3)

Investigator: Jeff, Leonie, Rosario

Aim of the experiment: Sequencing of RFP-Generator (RFC25, pSB1C3)

Procedure:

Sequencing batch were prepared after manufacturer's protocol. (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer)

Tuesday, April 23rd

Picking of of E. coli XL1 blue with Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3)

Investigator: Jeff, Leonie, Rosario, Florian

Aim of the experiment: Picking of of E. coli XL1 blue with Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3)

Procedure:

  • pSB1C3 plasmid with BBa_K801031 (PhyB 2 - 908 aa, RFC25): Colonies were picked from chloramphenicol plates.
  • Picked pipette tips was transferred into cell-culture tubes with air-permeable, sterile cover. Each tube contain 4 mL of LB-medium + 4 µL chloramphenicol(1000x).
  • 4 colonies were picked.
  • These tubes were transferred in a cell culture shaker at 37 °C and were incubated overnight

Analytical digestion and gelelectrophoresis of RFP-generator (RFC25, pSB1C3, P4 & P5)

Investigator: Jeff, Leonie, Rosario, Florian

Aim of the experiment: Analytical digestion and gelelectrophoresis of RFP-generator (RFC25, pSB1C3, P4 & P5).


Procedure:

  • Batch for analytical digestion for P4 with NgoMIV+AgeI-HF
volume reagent
2.5 µl Plasmid DNA P4
2 µl NEBuffer 4 (10x)
0.25 µl NgoMIV (10 U/µl)
0.25 µl AgeI-HF (20 U/µl)
15 µl ddH2O
=20 µl TOTAL
  • Batch for analytical digestion for P5 with NgoMIV+AgeI-HF
volume reagent
2.5 µl Plasmid DNA P5
2 µl NEBuffer 4 (10x)
0.25 µl NgoMIV (10 U/µl)
0.25 µl AgeI-HF (20 U/µl)
15 µl ddH2O
=20 µl TOTAL
  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed at 90 V for 60 min.

Results:

1 kbp ladder DNA ladder P4 P5
Mutation successful Mutation successful!
  • Parts are compliant and do not contain RFC25 forbidden restriction sites.


TUM13 20130423 RFP Generator RFC25 AgeI NgoMIV.png

Sequencing of pTUM vectors with pGAL, pADH, pTEF1, pTEF2

Investigator: Jeff, Leonie, Rosario, Florian

Aim of the experiment: Sequencing of pTUM vectors with pGAL, pADH, pTEF1, pTEF2

Procedure:

Sequencing batch were prepared after manufacturer's protocol. (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer).

The different vectors we sequenced received the following barcodes:
- ADH in pTUM100: FR01002265
- TEF1 in pTUM100: FR01002266
- TEF2 in pTUM100: FR01002266
- GAL in pTUM100: FR01002268

Sequencing of TEF2 in pTUM100 was not interpretable. The other sequences were consistent with the sequences in the parts registry.

Wednesday, April 24th

Miniprep of Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3)

Investigator: Jeff, Leonie, Florian

Aim of the experiment: Miniprep of Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3).

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)

Analytical digestion and gelelectrophoresis of Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3), P7 - P10

Investigator: Jeff, Leonie, Florian

Aim of the experiment: Analytical digestion and gelelectrophoresis of Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3), P7 - P10.

Procedure:

  • Batch for analytical digestion for P7 with NgoMIV+AgeI-HF
volume reagent
2.5 µl Plasmid DNA P7
2 µl NEBuffer 4 (10x)
0.25 µl NgoMIV (10 U/µl)
0.25 µl AgeI-HF (20 U/µl)
15 µl ddH2O
=20 µl TOTAL
  • Batch for analytical digestion for P8 with NgoMIV+AgeI-HF
volume reagent
2.5 µl Plasmid DNA P8
2 µl NEBuffer 4 (10x)
0.25 µl NgoMIV (10 U/µl)
0.25 µl AgeI-HF (20 U/µl)
15 µl ddH2O
=20 µl TOTAL
  • Batch for analytical digestion for P9 with NgoMIV+AgeI-HF
volume reagent
2.5 µl Plasmid DNA P9
2 µl NEBuffer 4 (10x)
0.25 µl NgoMIV (10 U/µl)
0.25 µl AgeI-HF (20 U/µl)
15 µl ddH2O
=20 µl TOTAL
  • Batch for analytical digestion for P10 with NgoMIV+AgeI-HF
volume reagent
2.5 µl Plasmid DNA P10
2 µl NEBuffer 4 (10x)
0.25 µl NgoMIV (10 U/µl)
0.25 µl AgeI-HF (20 U/µl)
15 µl ddH2O
=20 µl TOTAL
  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed at 90 V for 60 min.

Results:

1 kbp ladder DNA ladder P7 P8 P9 P10
Part is correct Part is correct Part is correct Part is correct


TUM13 20130424 PhytochromeB RFC25 AgeI NgoMIV.png

Transformation of E. coli XL1 blue with EreA and EreB (pDEST14)

Investigator: Jeff, Leonie, Florian

Aim of the experiment: Transformation of E. coli XL1 blue with EreA and EreB (pDEST14).

Procedure:

  • Plasmid DNA was received dried in paper from McMaster University.
  • DNA was resuspended in ddH2O
  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 2 µl of DNA was added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • The transformated cells were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated on chlorampenicol and ampicillin plates.

Week 2

Monday, April 29th

Miniprep of pRK792, pRK793, pRIL, ereA, ereB

Investigator: Leonie

Aim of the experiment: Miniprep of pRK792, pRK793, pRIL, ereA, ereB

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
  • Concentrations were determined by measuring the absorption:
Plasmid c [ng/µl]
pRK792 214,5
pRK793 154,3
pRIL 6,1
ereA 183,4
ereB 98,3
  • The procedure will have to be repeated for pRIL

Midiprep of RFC25 compatible RFP generator in (pSB1C3)

Investigator: Andreas, Florian

Aim of the experiment: Midiprep of RFC25 compatible RFP generator in (pSB1C3)

Procedure:

  • Midiprep was performed after manufacturer's protocol (QIAprep Midiprep, QIAGEN)

Tuesday, April 30th

Preparative digestion and gelelectrophoresis of mINF1 and Leptin with HindIII and EheI

Investigator: Louise, Johanna

Aim of the experiment: Testing the enzymes, since the earlier digestion with probably older enzymes did not work (no bands on gel) .

Procedure:

  • Batch for preparative digestion for mINF1 with HindIII and EheI
volume reagent
10 µl Plasmid DNA mINF11
5 µl Tango Buffer (10x)
2 µl HindIII (10 U/µl)
3 µl EheI (10 U/µl)
30 µl ddH2O
=50 µl TOTAL
  • Batch for preparative digestion for Leptin with HindIII and EheI
volume reagent
20 µl Plasmid DNA Leptin
5 µl Tango Buffer (10x)
2 µl HindIII (10 U/µl)
3 µl EheI (10 U/µl)
20 µl ddH2O
=50 µl TOTAL
  • Incubation for 3 h at 37 °C.

Transformation of E. coli XL1 blue with PSH21 (P17)

Investigator: Johanna, Louise

Aim of the experiment: Transformation of E. coli XL1 blue with PSH21.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice for 10 minutes.
  • 5 µl of DNA was added to 250 µl of competent cells and gently mixed.
  • 60 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding the DNA to 2 ml LB-medium.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • The transformated cells were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated on chlorampenicol and ampicillin plates.

Thursday, May 2nd

Miniprep of pSH21 (pAutoRex8) containing AlcR/AlcA promotor system

Investigator: Katrin

Aim of the experiment: Miniprep of pSH21 (pAutoRex8) containing AlcR/AlcA promotor system

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
  • The concentration was measured (900 ng/µl)


Friday, May 3rd

Transformation of E. coli XL1 blue with pSB1C3-GFP, pSB1C3-mkate2, pSB1C3-mCherry

Investigator: Andreas

Aim of the experiment: Transformation of E. coli XL1 blue with pSB1C3-GFP, pSB1C3-mkate2, pSB1C3-mCherry.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice for 10 minutes.
  • 5 µl of DNA was added to 250 µl of competent cells and gently mixed.
  • 60 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding the DNA to 2 ml LB-medium.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • The transformated cells were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated on chlorampenicol and ampicillin plates.

Plating of received E. coli containing biobricks

Investigator: Jeff, Andreas

Aim of the experiment: The received biobricks were already transformed in E. coli and were in an agar stabs. These E. coli cells were transferred with an inoculation loop on antibiotic selection plates and were incubated over night.

Operational sequence:

  • Bacterias containing plasmids with biobricks were transferred with a sterile inoculation loop on antibiotic plates and were incubated at 37 °C overnight.
  • The biobricks were:
Name Function
[[http://partsregistry.org/Part:BBa_K157004 BBa_K157004]] Fluoresceine A -binding derivative of a Lipocalin
[[http://partsregistry.org/Part:BBa_K863000 BBa_K863000]] bpul (laccase from Bacillus pumilus) with T7 promoter, RBS and HIS tag
[[http://partsregistry.org/Part:BBa_K909009 BBa_K909009]] cDNA of UV-B sensing protein UVR8 from Arabidopsis thaliana
[[http://partsregistry.org/Part:BBa_K337013 BBa_K337013]] constitutive promoter SV40
[[http://partsregistry.org/Part:BBa_K747096 BBa_K747096]] constitutive promoter CMV
[[http://partsregistry.org/Part:BBa_K414002 BBa_K414002]] constitutive promoter CaMV35S
[[http://partsregistry.org/Part:BBa_K147002 BBa_K147002]] xylE gene coding for catechol-1,2-dioxygenase
[[http://partsregistry.org/Part:BBa_E2020 BBa_E2020]] Cerulean
[[http://partsregistry.org/Part:BBa_K404319 BBa_K404319]] mCFP
[[http://partsregistry.org/Part:BBa_E0040 BBa_E0040]] GFPmut3b
[[http://partsregistry.org/Part:BBa_K592010 BBa_K592010]] amilGFP
[[http://partsregistry.org/Part:BBa_E2050 BBa_E2050]] mOrange
[[http://partsregistry.org/Part:BBa_K399001 BBa_K399001]] mStrawberry
[[http://partsregistry.org/Part:BBa_E1010 BBa_E1010]] mRFP1
[[http://partsregistry.org/Part:BBa_E2060 BBa_E2060]] mCherry
[[http://partsregistry.org/Part:BBa_K592012 BBa_K592012]] eforRed
[[http://partsregistry.org/Part:BBa_K592011 BBa_K592011]] cjBlue
[[http://partsregistry.org/Part:BBa_K864401 BBa_K864401]] aeBlue
[[http://partsregistry.org/Part:BBa_K592009 BBa_K592009]] amilCP, blue chromoprotein
[[http://partsregistry.org/wiki/index.php?title=Part:BBa_K414000 BBa_K414000]] RD29A Promoter + Strong Plant Kozak (RBS) + RFP
[[http://partsregistry.org/wiki/index.php?title=Part:BBa_K414006 BBa_K414006]] 35S Promoter + (Strong Plant RBS + GFP) From K414001
[[http://partsregistry.org/wiki/index.php?title=Part:BBa_K414007 BBa_K414007]] DREB1C promoter
[[http://partsregistry.org/wiki/index.php?title=Part:BBa_K678001 BBa_K678001]] alcA promoter
[[http://partsregistry.org/Part:BBa_K243004 BBa_K243004]] Short linker
[[http://partsregistry.org/Part:BBa_K243005 BBa_K243005]] Middle linker
[[http://partsregistry.org/Part:BBa_K243006 BBa_K243006]] Long Linker
[[http://partsregistry.org/Part:BBa_K243029 BBa_K243029]] GSAT Linker
[[http://partsregistry.org/Part:BBa_K243030 BBa_K243030]] SEG Linker

Sunday, May 5th

Picking of the plated E. coli containing biobricks and the parts received from LMU

Investigator: Florian

Aim of the experiment: The colonies from the plates were transferred into liquid LB medium, so that minipreps can be performed the next day.

Operational sequence:

  • Tubes with 5 ml LB medium and the corresponding antibiotic were prepared.
  • A single colony from each plate was transferred into a tube with a pipet tip.
  • The biobricks were:
Label Name Function
p19 mCherry in pSB1C3
p20 [[http://partsregistry.org/Part:BBa_K823039 BBa_K823039]] GFP in pSB1C3
p21 [[http://partsregistry.org/Part:BBa_K823029 BBa_K823029]] mKate2 in pSB1C3
p22 [[http://partsregistry.org/wiki/index.php?title=Part:BBa_K414006 BBa_K414006]] 35S Promoter + (Strong Plant RBS + GFP) From K414001
p23 [[http://partsregistry.org/Part:BBa_K414002 BBa_K414002]] constitutive promoter CaMV35S
p24 [[http://partsregistry.org/Part:BBa_K909009 BBa_K909009]] cDNA of UV-B sensing protein UVR8 from Arabidopsis thaliana
p25 [[http://partsregistry.org/Part:BBa_K399001 BBa_K399001]] mStrawberry
p26 [[http://partsregistry.org/wiki/index.php?title=Part:BBa_K414007 BBa_K414007]] DREB1C promoter
p27 [[http://partsregistry.org/Part:BBa_K863000 BBa_K863000]] bpul (laccase from Bacillus pumilus) with T7 promoter, RBS and HIS tag
p28 [[http://partsregistry.org/Part:BBa_K337013 BBa_K337013]] constitutive promoter SV40
p29 [[http://partsregistry.org/Part:BBa_K592011 BBa_K592011]] cjBlue
p30 [[http://partsregistry.org/wiki/index.php?title=Part:BBa_K678001 BBa_K678001]] alcA promoter
p31 [[http://partsregistry.org/Part:BBa_K592012 BBa_K592012]] eforRed
p32 [[http://partsregistry.org/Part:BBa_K592010 BBa_K592010]] amilGFP
p33 [[http://partsregistry.org/Part:BBa_K864401 BBa_K864401]] aeBlue
p34 [[http://partsregistry.org/Part:BBa_K404319 BBa_K404319]] mCFP
p35 [[http://partsregistry.org/wiki/index.php?title=Part:BBa_K414000 BBa_K414000]] RD29A Promoter + Strong Plant Kozak (RBS) + RFP
p36 [[http://partsregistry.org/Part:BBa_K592009 BBa_K592009]] amilCP, blue chromoprotein
p37 [[http://partsregistry.org/Part:BBa_K747096 BBa_K747096]] constitutive promoter CMV
p38 [[http://partsregistry.org/Part:BBa_K147002 BBa_K147002]] XylE dioxygenase (catechol dioxygenase)
p39 [[http://partsregistry.org/Part:BBa_K243005 BBa_K243005]] Middle linker
p40 [[http://partsregistry.org/Part:BBa_K243029 BBa_K243029]] GSAT Linker
p41 [[http://partsregistry.org/Part:BBa_E0040 BBa_E0040]] GFPmut3b
p42 [[http://partsregistry.org/Part:BBa_K243006 BBa_K243006]] Long Linker
p43 [[http://partsregistry.org/Part:BBa_K243030 BBa_K243030]] SEG Linker
p44 [[http://partsregistry.org/Part:BBa_K243004 BBa_K243004]] Short linker
p45 [[http://partsregistry.org/Part:BBa_K157004 BBa_K157004]] Fluoresceine A -binding derivative of a Lipocalin
p46 [[http://partsregistry.org/Part:BBa_E2060 BBa_E2060]] mCherry
p47 [[http://partsregistry.org/Part:BBa_E2020 BBa_E2020]] Cerulean
p48 [[http://partsregistry.org/Part:BBa_E1010 BBa_E1010]] mRFP1
p49 [[http://partsregistry.org/Part:BBa_E2050 BBa_E2050]] mOrange
  • There were no colonies on the plate with K864401 (p33), therefore the LB medium could not be infected
  • The tubes were placed into the incubator at 37 °C

Week 3

Monday, May 6th

Miniprep of the prepared E. coli containing biobricks and the parts from LMU

Investigators: Florian, Johanna, Jefferey

Aim of the experiment: A miniprep of the overnight culture of our E. coli containig our biobricks and LMU parts was performed using the Qiagen miniprep kit.

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
  • Resulting concentrations were determined by measuring the absorption:
Label Name Concentration [ng/µl]
p19 mCherry in pSB1C3 40,2
p20 GFP in pSB1C3 58,5
p21 mKate2 in pSB1C3 131,3
p22 35S Promoter + (Strong Plant RBS + GFP) From K414001 42,8
p23 constitutive promoter CaMV35S 39,3
p24 cDNA of UV-B sensing protein UVR8 from Arabidopsis thaliana 30,0
p25 mStrawberry 46,6
p26 DREB1C promoter 34,8
p27 bpul (laccase from Bacillus pumilus) with T7 promoter, RBS and HIS tag 52,5
p28 constitutive promoter SV40 58,7
p29 cjBlue 44,4
p30 alcA promoter 26,9
p31 eforRed 64,8
p32 amilGFP 59,3
p34 mCFP 78,4
p35 RD29A Promoter + Strong Plant Kozak (RBS) + RFP 61,2
p36 amilCP, blue chromoprotein 89,2
p37 constitutive promoter CMV 83,6
p38 XylE dioxygenase (catechol dioxygenase) 57,4
p39 Middle linker 64,3
p40 GSAT Linker 109,6
p41 GFPmut3b 118,1
p42 Long Linker 133,0
p43 SEG Linker 107,5
p44 Short linker 60,2
p45 Fluoresceine A -binding derivative of a Lipocalin 82,7
p46 mCherry 230,2
p47 Cerulean 25,7
p48 mRFP1 299,3
p49 mOrange 181,2


Sequencing of FluA, SV40, CaMV35S, xylE, LMU mKate2, LMU GFP, LMU mCherry, DREB1C, RD29A

Investigators: Andreas, Florian, Johanna, Jefferey, Rosario

Aim of the experiment: Sequencing of genes for which no prior sequencing results were available.

Procedure: The DNA was prepared for sequencing according to the Eurofins SmartSeq Kit protocol (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer).

The different genes we sequenced received the following barcodes:

Label Name Barcode
p45 FluA FR01002355
p28 SV40 FR01002356
p23 CaMV35S FR01002357
p38 xylE FR01002358
p21 LMU mKate2 FR01002359
p20 LMU GFP FR01002360
p19 LMU mCherry FR01002345
p46 mCherry FR01002346
p26 DREB1C FR01002347
p35 RD29A FR01002348

Preparation of ordered primers

Investigators: Andreas, Jefferey, Rosario

Aim of the experiment: Dissolving of primer pallets to provide a concentration of 100 pmol/µl

Procedure: We added an amount of water which gave us a final primer concentration of 100 pmol/µl.

Primers were labeled as follows:

Label Oligonr.
6 EreA_for
7 EreA_rev
8 EreA_SDM1_for
9 EreA_SDM1_rev
10 EreA_SDM2_for
11 EreA_SDM2_rev
12 EreA_SDM3_for
13 EreA_SDM3_rev
14 EreB_for
15 EreB_rev
16 EreB_SDM1_for
17 EreB_SDM1_rev
18 EreB_SDM2_for
19 EreB_SDM2_rev
20 EreB_SDM3_for
21 EreB_SDM3_rev

Tuesday, May 7th

PCR, purification and analytical geleletrophoresis of EreA (P15) and EreB (P16)

Investigator: Jeff, Louise, Florian, Rosario, Andi, Johanna

Aim of the experiment: PCR of EreA (P15) and EreB (P16).

Procedure:

Operational sequence:

  • PCR reaction mixture
volume reagent
10 µl 5x OneTaq Standard Reaction Buffer
1 µl 10 mM dNTPs
1 µl 10 µM Forward Primer (P15: O46 (EreA_for); P16: O31 (EreB_for))
1 µl 10 µM Reverse Primer (P15: O47 (EreA_rev); P16: O32 (EreB_rev))
0.25 µL OneTaq Hot Start DNA Polymerase (Finally: 1.25 units/50 µL)
1 µl Plasmid DNA (P15; P16)
35.75 µL ddH2O Water
=50 µL TOTAL
  • Mix with pipette
  • The gradient PCR program was performed after following scheme with following conditions (Tm=54 °C; ΔG=2 °C; P15 in row 11(=52 °C); P16 in row 1 (=54.0 °C)):
Initial denaturation 94 °C 30 s
30 cycles 94 °C 30 s
Tm=54 °C; ΔG=2 °C 60 s
68 °C 80 s
Final extension 68 °C 5 min
Hold 4 °C infinite
  • After PCR, the product was purified with QIAquick PCR Purification Kit, Qiagen.
  • 9 µl of the purified PCR products were mixed with 1 µl DNA loading buffer (10x) for analytical gelelectrophoresis
  • Analytical gelelectrophoresis was performed at 90 V for 60 min in 1% agarose gel.
1 kbp ladder F1 F2
Fragment-size like expected Fragment-size like expected

TUM13 20130507 P15 P16 PCR.png

Preparative digestion and gelelectrophoresis of PhyB (P9) and PIF3-20aa linker (P50) with AgeI and PstI as well as 20aalinker-PIF3 (P51) with EcoRI and NgoMIV

Investigator: Jeff, Andi, Florian, Rosario, Louise, Johanna

Aim of the experiment: Preparative digestion and gelelectrophoresis of PhyB (P9) and PIF3-20aa linker (P50) with AgeI and PstI as well as 20aalinker-PIF3 (P51) with EcoRI and NgoMIV .

Procedure:

  • Batch for preparative digestion of PhyB (P9) and PIF3-20aa linker (P50) with AgeI and PstI
volume reagent
20 µl Plasmid DNA P9/P50
4 µl NEBuffer 4
0.4 µl BSA (100x)
1 µl AgeI-HF
1 µl PstI-HF
13.6 µl ddH2O
=40 µl TOTAL
  • Batch for preparative digestion of 20aalinker-PIF3 (P51) with EcoRI and NgoMIV
volume reagent
20 µl Plasmid DNA P51
4 µl NEBuffer 4
1 µl EcoRI-HF
1 µl NgoMIV
14 µl ddH2O
=40 µl TOTAL
  • Incubation for 3 h at 37 °C.
  • 4 µl of DNA loading buffer (10x) were added to the reaction batches after digestion and were loaded on an 1% low-melting agarose gel for preparative gelelectrophoresis.
  • Preparative gelelectrophoresis was performed at 70 V for 90 min.
P9 digestion = F3 1 kbp ladder P50 digestion = F4 P51 digestion = F5
Fragment-size like expected; band was cut out Fragment-size like expected; band was cut out Fragment-size like expected; band was cut out

TUM13 20130507 P9 AgeI.PstI P50 AgeI.PstI P51 EcoRI.NgoMIV.png

  • Bands were extracted by QIAquick Gel Extraction Kit, QIAGEN.

Wednesday, May 8th

Preparative digestion and gelelectrophoresis of PCR product of EreA (F1) and EreB (F2) with XbaI & AgeI

Investigator: Jeff, Andi, Florian, Rosario, Louise

Aim of the experiment: Preparative digestion and gelelectrophoresis of PCR product of EreA (F1) and EreB (F2) with XbaI & AgeI.

Procedure:

  • Batch for preparative digestion of PCR product of EreA (F1) and EreB (F2) with XbaI & AgeI.
volume reagent
25 µl PCR product F1/F2
5 µl NEBuffer 4
0.5 µl BSA (100x)
1 µl AgeI-HF
1 µl XbaI
17.5 µl ddH2O
=50 µl TOTAL
  • Batch for preparative digestion of P52 for preperation of pSB1C3 vector:
volume reagent
20 µl Plasmid DNA P52
4 µl NEBuffer 4
0.4 µl BSA (100x)
1 µl AgeI-HF
1 µl XbaI
13.6 µl ddH2O
=40 µl TOTAL
  • Incubation for 3 h at 37 °C.
  • 5 µl of DNA loading buffer (10x) were added to the reaction batches for F1 & F2 and 4 µl of DNA loading buffer (10x) were added to the reaction batches for Pxx after digestion and were loaded on an 1% agarose gel for preparative gelelectrophoresis.
  • Preparative gelelectrophoresis was performed at 90 V for 60 min.
F1 digestion = F6 F2 digestion = F7 1 kbp ladder P52 digestion = F8
Length was like expected Length was like expected Length was like expected; the lower band was extracted

TUM13 20130508 F1 F2 P52 Xb.png

  • Bands were extracted by QIAquick Gel Extraction Kit, QIAGEN.

Ligation of F8+F6 (EreA in pSB1C3), F8+F7 (EreB in pSB1C3)

Investigator: Jeff, Andi, Florian, Rosario, Louise

Aim of the experiment: Ligation of F8+F6 (EreA in pSB1C3), F8+F7 (EreB in pSB1C3). Quickchanges have still to be performed.

Procedure:

Ligation batch for F8+F6 (EreA in pSB1C3), F8+F7 (EreB in pSB1C3):

  • Ligation batch for F8+F6
volume reagent
1.35 µl F8 (74.3 ng/µl, 2086 bp)
6.76 µl F6 (25.9 ng/µl, 1218 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
8.89 µl ddH2O
=20 µl TOTAL
  • Ligation batch for F8+F7
volume reagent
1.35 µl F8 (74.3 ng/µl, 2086 bp)
8.78 µl F7 (20.6 ng/µl, 1257 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
6.87 µl ddH2O
=20 µl TOTAL
  • Negative control was als prepared. Instead of the insert, the same volume of ddH2O was added to the reaction batches.
  • Cycled ligation has been performed after following protocol in a thermocycler:
100 cycles 12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
Hold 16 °C infinite


Lid temperature = 37 °C

Midiprep of cloning vector RFC25 RFP generating device

Investigators: Andreas, Rosario

Aim of the experiment: Midiprep of our cloning vector RFC25 RFP generating device.

Procedure: Midiprep was performed after manufacturer's protocol (QIAprep Midiprep, QIAGEN)

The yield of our vector was 1854 ng.

Thursday, May 9th

Transformation of E. coli XL1 blue with F8(pSB1C3)+F6(EreA) and F8(pSB1C3)+F7(EreB)

Investigator: Florian, Jeff, Leonie, Louise, Katrin, Ingmar

Aim of the experiment: Transformation of E. coli XL1 blue with F8(pSB1C3)+F6(EreA) and F8(pSB1C3)+F7(EreB). Quickchanges has now to be performed to remove forbidden restriction sites.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 10 µl of ligation products F8+F6, F8+F7, F8 negative control were added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

Friday, May 10th

Quick Change mutagenesis to remove mutations found by sequencing in our gene constructs

Investigator: Andi, Jeff, Rosario

Aim of the experiment: Deletion of found mutations.

Operational sequence

1. PCR general setup
Reaction batch 1

volume reagent
2.5 µl 10x Pfu Ultra II buffer
4 µl DNA template
1 µl 1:10 dilution of appropriate Oligo (= 5 pmol)
16.5 µl ddH2O
0.5 µl dNTP mix
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)

Reaction batch 2

volume reagent
2.5 µl 10x Pfu Ultra II buffer
4 µl DNA template
1 µl 1:10 dilution of appropriate Oligo (= 5 pmol)
16.5 µl ddH2O
0.5 µl dNTP mix
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)


PCR cycling parameters

Segment Cycles Temperature Time
1 1 95 °C 30 sec
2 12 95 °C 30 s
55 °C 1 min
68 °C 6 min
  • Having completed the PCR cycling parameters listed above both PCR reaction batches were mixed together and the cycling parameters listed above were one time more applied.
  • After the PCR was finished 1 µl of the DpnI restriction enzyme (10 U/µl)was added
  • Now the reaction was mixed gently and thoroughly, spinned down in a microcentrifuge for 1 minute, and immediately incubated at 37 °C for 1 hour to digest the parental supercoiled dsDNA


2. Used constructs and primers

Quickchange number Plasmid number Geneconstruct Oligo number
QC 1P27BPul_Laccase+ pSB1C3O26 & O27

Picking of transformed Plasmids F8 + F6

Investigator: Andi

Aim of the study: Picking from the overnight transformation of the ligated F8+F6, to see whether ligation is successful or not.

Operational sequence:

  • Picking and overnight culture after standard laboratory's protocol. (CamR LB-medium)

PCR of TEV (P14, pRK793)

Investigator: Katrin, Jeff

Aim of the experiment: PCR, purification and analytical geleletrophoresis of TEV (P14, pRK793) to produce TEV with RFC25 pre- and suffx (still contains forbidden SpeI-site).

Procedure:

Operational sequence:

  • PCR reaction mixture
volume reagent
10 µl 5x OneTaq Standard Reaction Buffer
1 µl 10 mM dNTPs
1 µl 10 µM Forward Primer (O34 (TEV_fw))
1 µl 10 µM Reverse Primer (O35 (TEV_rv))
0.25 µL OneTaq Hot Start DNA Polymerase (Finally: 1.25 units/50 µL)
1 µl Plasmid DNA (P14)
35.75 µL ddH2O Water
=50 µL TOTAL
  • Mix with pipette
  • The PCR program was performed after following scheme with following conditions:
Initial denaturation 94 °C 30 s
30 cycles 94 °C 30 s
55 °C 60 s
68 °C 150 s
Final extension 68 °C 5 min
Hold 4 °C infinite
  • After PCR, the product was purified with QIAquick PCR Purification Kit, Qiagen.
  • Resulting product was labeled as F12.

Digestion of P61 with S1 Nuclease

Investigator: Katrin

Oligohybridization of O22 (MinMCS_for) and O23 (MinMCS_rev)

Investigator: Leonie


Preparation of ordered primers

Investigators: Andreas, Rosario, Katrin, Ingmar

Aim of the experiment: Dissolving of primer pallets to provide a concentration of 100 pmol/µl

Procedure: We added an amount of water which gave us a final primer concentration of 100 pmol/µl.

Primers were labeled as follows:

Label Oligonr.
24 BPU_for
25 BPU_rev
26 BPU_SDM1_for
27 BPU_SDM1_rev
28 BPU_SDM2_for
29 BPU_SDM2_rev
30 BPU_SDM3_for
31 BPU_SDM3_rev
32 BPU_SDM4_for
33 BPU_SDM4_rev
34 TEV_for
35 TEV_rev
36 TEV_t387c_for
37 TEV_t387c_rev
38 N_Split_TEV_for
39 N_Split_TEV_rev
40 C_Split_TEV_for
41 C_Split_TEV_rev
42 PIF6_2-100_for
43 PIF6_2-100_rev
44 p104AgeI a71g fw
45 p104AgeI a71g rev
46 xylE_for
47 xylE_rev
48 xylE_c312a_for
49 xylE_c312a_rev
50 xylE_g483a_for
51 xylE_g483a_rev
52 xylE_a834g_for
53 xylE_a834g_rev

Saturday, May 11th

Preparative digestion of PCR product of S219V pRK793 (F12) with XbaI & AgeI

Investigator: Louise

Aim of the experiment: Preparative digestion of PCR product of S219V pRK793 (F12) with XbaI & AgeI. Quickchange has still to be performed (forbidden SpeI restriction site).

Procedure:

  • Batch for preparative digestion of PCR product S219V pRK793 (F12) with XbaI & AgeI.
volume reagent
20 µl PCR product F12
4 µl NEBuffer 4
0.4 µl BSA (100x)
1 µl AgeI-HF
1 µl XbaI
13.6 µl ddH2O
=40 µl TOTAL
  • Incubation for 3 h at 37 °C
  • Digested products were purified to remove nucleotides and enzymes with QIAquick PCR Purification Kit, QIAGEN.
  • The digested fragment was labelled F15

Miniprep of overnight culture of transformated E.~coli XL1-Blue with F8 (pSB1C3) + F6 (EreA)

Investigator: Louise

Aim of the experiment: Miniprep of overnight culture of transformated E.~coli XL1-Blue with F8 (pSB1C3) + F6 (EreA) of 2 clones picked the day before

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
  • The plasmids were labelled as P63 and P64

Analytical digestion and gelelectrophoresis of P63 and P64 with AgeI-HF and XbaI

Investigator: Louise

Aim of the experiment: Analytical digestion and gelelectrophoresis of P63 and P64 with AgeI-HF and XbaI

Procedure:

  • Batch for analytical digestion of P63 and P64 with AgeI-HF and XbaI
volume reagent
2.5 µl Plasmid DNA P63/P64
2 µl NEBuffer 4 (10x)
0.2 µl BSA (100x)
0.25 µl XbaI(10 U/µl)
0.25 µl AgeI-HF (20 U/µl)
14.8 µl ddH2O
=20 µl TOTAL
  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed at 90 V for 60 min.


Analytical digestion of P63 with AgeI-HF and XbaI 1 kbp ladder Analytical digestion of P64 with AgeI-HF and XbaI
Insertion successful Insertion successful

TUM13 20130511 P63 P64 XbaI.png

Preparative digestion of PCR product of EreB (F2) with XbaI & AgeI

Investigator: Louise,Leonie,Johanna

Aim of the experiment: Preparative digestion of PCR product EreB (F2) with XbaI & AgeI (second try since there did not grow any transformed bacteria in the first time).

Procedure:

  • Batch for preparative digestion of PCR product and EreB (F2) with XbaI & AgeI.
volume reagent
20 µl PCR product F2
5 µl NEBuffer 4
0.5 µl BSA (100x)
1 µl AgeI-HF
1 µl XbaI
22.5 µl ddH2O
=50 µl TOTAL
  • Incubation for 3 h at 37 °C
  • The digested fragment was labelled F14


Purification and ligation of digested PCR product EreB (F14)

Investigator: Louise, Rosario

Aim of the experiment: PCR Purification and ligation of digested PCR product EreB (F14).

Procedure: PCR Purification of EreB PCR (F14)

  • To purify the digested Fragment(F14) the QIAquick PCR Purification Kit was used. The concentration of the purified product was found to be 5 ng/µl via Nano drop.

Ligation of F14 + F8(pSB1C3)

  • Ligation batch for F8+F14 (positive control)
volume reagent
1.35 µl F8 (74.3 ng/µl, 2086 bp)
15.65 µl F14 (5 ng/µl, 1257 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
=20 µl TOTAL
  • Negative control was also prepared. Instead of the insert, the same volume of ddH2O was added to the reaction batch.
  • Cycled ligation has been performed after following protocol in a thermocycler:
99 cycles 12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
Hold 16 °C infinite


Lid temperature = 37 °C

Transformation of ligation products of F10 + F11 into E.coli Xl1-Blue

Investigator: Andi

Aim of the experiment:Transformation of the ligation products of F10 + F11 and the negative control in pTUM104 in XL1 Blue.

Operation Sequence

  • melting of 2x 200 µl Ca-competent E.coli XL1-Blue cells on ice
  • Preparing 4 Tubes with 100 µl of Ca-competent E.coli XL1-Blue cells
  • addition of 5 µl of the ligation products
  • incubation for 30 min on ice
  • heat shock for 5 min at 37 °C
  • transfer of cells to 1 ml LB-medium without antibiotics and incubate at 37°C and 180 rpm for 30 min
  • plate 100 µl on an Amp-LB-plate
  • sediment the leftover in a centrifuge (30 - 60 sec, 13 000 rpm) and resuspend the sediment in 100 µl LB-medium and plate it as well on an Amp-LB-plate

Transformation of Quickchange Product P62 into E.coli Xl1-Blue

Investigator: Andi

Aim of the experiment:Transformation of the Quickchange Product P62 and the negative control in XL1 Blue.

Operation Sequence

  • melting of 1x 200 µl Ca-competent E.coli XL1-Blue cells on ice
  • Preparing 4 Tubes with 50 µl of Ca-competent E.coli XL1-Blue cells
  • addition of 1 µl of the Quickchange Product
  • incubation for 30 min on ice
  • heat shock for 5 min at 37 °C
  • transfer of cells to 1 ml LB-medium without antibiotics and incubate at 37°C and 180 rpm for 30 min
  • plate 100 µl on an Amp-LB-plate
  • sediment the leftover in a centrifuge (30 - 60 sec, 13 000 rpm) and resuspend the sediment in 100 µl LB-medium and plate it as well on an Amp-LB-plate

Quickchange mutagenesis of pTUM104

Investigator: Ingmar

Aim of the experiment: Sequencing results showed a forbiden AgeI restriction site in this vector. The sdm will delete this restricition site

Procedure: PCR
Reaction batch 1

volume reagent
2.5 µl 10x Pfu Ultra II buffer
4 µl Plasmid P6 template
0.5 µl 1:10 dilution of O44 (10 pmol/µL)
16.5 µl ddH2O
0.5 µl dNTP mix
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)

Reaction batch 2

volume reagent
2.5 µl 10x Pfu Ultra II buffer
4 µl Plasmid P6 template
0.5 µl 1:10 dilution of O45 (10 pmol/µL)
16.5 µl ddH2O
0.5 µl dNTP mix
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)

PCR cycling parameters

Segment Cycles Temperature Time
1 1 95 °C 30 sec
2 10 95°C 30 sec
55°C 1 min
67°C 6 min
  • Having completed the PCR cycling parameters listed above both PCR reaction batches were mixed together and the cycling parameters listed above were one time more applied.
  • Digestion of the parental DNA with DpnI: Addition of 1 µl DpnI to the PCR batch and incubate for 1 h at 37 °C. The resulting product was named fragmet 14.

Transformation into E.coli Xl1-Blue Operation Sequence

  • melting of 100 µl Ca-competent E.coli XL1-Blue cells on ice
  • addition of 1 µl of the PCR product
  • incubation for 30 min on ice
  • heat shock for 5 min at 37 °C
  • transfer of cells to 1 ml LB-medium without antibiotics and incubate at 37°C and 180 rpm for 30 min
  • plate 100 µl on an Amp-LB-plate
  • sediment the leftover in a centrifuge (30 - 60 sec, 13 000 rpm) and resuspend the sediment in 100 µl LB-medium and plate it as well on an Amp-LB-plate

Sunday, May 12th

Analytical gelelectrophoresis of F15 (digested TEV PCR product)

Investigator: Jeff, Rosario

Aim of the experiment: Analytical gelelectrophoresis of F15 (digested TEV PCR product) to check whether PCR has worked.

Procedure:

  • 5 µl of F15 was mixed with 0.55 µl of DNA loading buffer (10x) and analytical gelelectrophoresis was performed at 1% agarose gel for 60 min at 90 V.

TUM13 20130512 PCR F12.png

  • PCR product has expected length

Transformation of E. coli XL1 blue with ligation product F8+F15 (TEV in pSB1C3, RFC25)

Investigator: Jeff, Rosario

Aim of the experiment: Transformation of E. coli XL1 blue with ligation product F8+F15 (TEV in pSB1C3, RFC25). Further quickchanges still have to be done.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 10 µl of the ligation products were added to 200 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

Transformation of E. coli XL1 blue with ligation products F8+F14 (EreB in pSB1C3, RFC25)

Investigator: Jeff, Rosario

Aim of the experiment: Transformation of E. coli XL1 blue with ligation product F8+F14 (EreB in pSB1C3, RFC25). Further quickchanges still have to be done.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 10 µl of the ligation products were added to 200 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

Transformation of E. coli XL1 blue with P23

Investigator: Jeff, Rosario

Aim of the experiment: Transformation of E. coli XL1 blue with P23 for insertion of miniMCS.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 2 µl of DNA was added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.


Picking of transformed Plasmid F10+F11 (IRES from polio virus, blunt ligated with pSB1C3 for sequencing)

Investigator: Andi

Aim of the study: Picking of transformed Plasmid F10+F11 (AlcR blunt ligated with pSB1C3 for sequencing).

Operational sequence:

  • Picking and overnight culture after standard laboratory's protocol. (CamR LB-medium)
  • 10 colonies were picked.

Week 4

Monday, May 13th

Miniprep of overnight culture of transformated E.~coli XL1-Blue with F10+F11

Investigator: Rosario, Jeffery, Johanna, Flo, Leonie

Aim of the experiment: Miniprep of overnight culture of transformated E.~coli XL1-Blue F10+F11 of 10 clones picked the day before

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)

Analyzing sequencing results

Investigator: Leonie,Johanna

Aim of the experiment: Comparison of the sequencing results with the Biobrick (BB) sequences.

Procedure: Using Geneious to align the sequencing results with the BB sequences.

LMU GFP in RFC 25(p20)

  • The provided sequence in the parts registry is totally wrong.
  • The comparison of the amino acid seqeunces reveals several point mutations.

TUM13 AlignmentforLMUGFP.png

FluA in RFC 25 (p45)

  • Did not yield sequencing results (does the primer bind ?)
  • No presence of RCF 25 standard restriction enzymes

mCherry in RFC 25 (p46)

  • Did not yield sequencing results (does the primer bind ?)
  • No presence of RCF 25 standard restriction enzymes

CaMV35S in RFC 25 (p23)

  • high identity
  • high match with HQ699544 (Blast)

LMU mKate2in RFC 25 (p21)

  • no continous ORF
  • Did not yield sequencing results

DREB1C promoter in RFC 25 (p26)

  • Present of fluorecent protein gene

xylE in RCF 25 (p38)

  • Did not yield sequencing results

SV40 in RCF 25 (p28)

  • sequencing result agrees with the laccases
  • the sequencing result can't be the one of SV40

Quickchange mutagenesis SDMI of p27

Investigator: Rosario, Jeff, Flo, Andi

Aim of the experiment: Sequencing results showed a forbidden restriction site in this vector. The sdm will delete this restricition site. The resulting Plasmid was labeled 65.

Procedure: PCR
Reaction batch 1

volume reagent
2.5 µl 10x Pfu Ultra II buffer
0.5 µl Plasmid P27 template
0.5 µl 1:10 dilution of O26 (10 pmol/µL)
20. 5 µl ddH2O
0.5 µl dNTP mix
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)

Reaction batch 2

volume reagent
2.5 µl 10x Pfu Ultra II buffer
0.5 µl Plasmid P27 template
0.5 µl 1:10 dilution of O27 (10 pmol/µL)
20.5 µl ddH2O
0.5 µl dNTP mix
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)

PCR cycling parameters

Segment Cycles Temperature Time
1 1 95 °C 30 sec
2 10 95°C 30 sec
55°C 1 min
67°C 4 min
  • Having completed the PCR cycling parameters listed above both PCR reaction batches were mixed together and the cycling parameters listed above were one time more applied, but the amount of cycles was increased to 20
  • Digestion of the parental DNA with DpnI: Addition of 1 µl DpnI to the PCR batch and incubate for 1 h at 37 °C.

Quickchange mutagenesis SDMI of p38

Investigator: Jeff, Flo, Andi, Rosario

Aim of the experiment: Sequencing results showed a forbidden restriction site in this vector. The sdm will delete this restricition site. The resulting Plasmid was labeled 67.

Procedure: PCR
Reaction batch 1

volume reagent
2.5 µl 10x Pfu Ultra II buffer
0,5 µl Plasmid P38 template
0.5 µl 1:10 dilution of O48 (10 pmol/µL)
20.5 µl ddH2O
0.5 µl dNTP mix
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)

Reaction batch 2

volume reagent
2.5 µl 10x Pfu Ultra II buffer
0.5 µl Plasmid P38 template
0.5 µl 1:10 dilution of O49 (10 pmol/µL)
20.5 µl ddH2O
0.5 µl dNTP mix
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)

PCR cycling parameters

Segment Cycles Temperature Time
1 1 95 °C 30 sec
2 10 95°C 30 sec
55°C 1 min
67°C 4 min
  • Having completed the PCR cycling parameters listed above both PCR reaction batches were mixed together and the cycling parameters listed above were one time more applied, but the amount of cycles have been increased to 20
  • Digestion of the parental DNA with DpnI: Addition of 1 µl DpnI to the PCR batch and incubate for 1 h at 37 °C.

Quickchange mutagenesis SDMI of P63

Investigator: Jeff, Rosario, Flo, Andi

Aim of the experiment: Sequencing results showed a forbidden restriction site in this vector. The sdm will delete this restricition site. The resulting Plasmid was labeled P66.

Procedure: PCR
Reaction batch 1

volume reagent
2.5 µl 10x Pfu Ultra II buffer
0.25 µl Plasmid P63 template; 1:2 dilution
0.5 µl 1:10 dilution of O8 (10 pmol/µL)
20.75 µl ddH2O
0.5 µl dNTP mix
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)

Reaction batch 2

volume reagent
2.5 µl 10x Pfu Ultra II buffer
0.25 µl Plasmid P63 template; 1:2 dilution
0.5 µl 1:10 dilution of O9 (10 pmol/µL)
20.75 µl ddH2O
0.5 µl dNTP mix
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)

PCR cycling parameters

Segment Cycles Temperature Time
1 1 95 °C 30 sec
2 10 95°C 30 sec
55°C 1 min
67°C 6 min
  • Having completed the PCR cycling parameters listed above both PCR reaction batches were mixed together and the cycling parameters listed above were one time more applied, the amount of cycles was raised to 20
  • Digestion of the parental DNA with DpnI: Addition of 1 µl DpnI to the PCR batch and incubate for 1 h at 37 °C.

Transformation of E. coli XL1 blue with P65

Investigator: Jeff, Rosario, Johanna, Andi, Flo, Leonie

Aim of the experiment: Transformation of E. coli XL1 blue with P65 .

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 2 µl of DNA was added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

Transformation of E. coli XL1 blue with P66

Investigator: Jeff, Rosario, Flo, Johanna, Andi, Leonie

Aim of the experiment: Transformation of E. coli XL1 blue with P66.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 2 µl of DNA was added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

Transformation of E. coli XL1 blue with P67

Investigator: Jeff, Rosario, Johanna, Andi, Leonie, Flo

Aim of the experiment: Transformation of E. coli XL1 blue with P67.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 2 µl of DNA was added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

Tuesday, May 14th

Analytical digestion of P15 and P19 to P52

Investigator: Leonie, Florian, Johanna

Aim of the experiment: Analytical digestion and gelelectrophoresis of P15 and P19 to P52 to check the sequencing results.

Procedure:

  • Batch for analytical digestion of P15 and P19 to P52
volume reagent
5 µl Plasmid DNA
5 µl Mastermix
=10 µl TOTAL

Batch of Mastermix

volume reagent
40 µl NEBuffer 4 (10x)
4 µl BSA (100x)
0.2 µl NotI(10 U/µl)
148 µl ddH2O
=200 µl TOTAL
  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed at 90 V for 60 min.

Gel 1

Gel 2

  • Discussion:
  • Gel 1, Row 1:
lane part plasmid band 1 band 2 result
2 EreA pDEST14 3,25 kb no cut, no restriction sites in pDEST14
3 mCherry(LMU) pSB1C3 2,0 kb 750 bp probably right
4 GFP(LMU)(845 bp) pSB1C3 2,0 kb 750 bp maybe switched with mKate2(LMU)
5 mKate2(LMU)(702 bp) pSB1C3 2,0 kb 900 bp maybe switched with GFP(LMU)
6 35S + Strong Plant + GFP(1775 bp) pSB1C3 2,0 kb 750 bp ?
7 UVR8(1332 bp) pSB1C3 2,0 kb 1,1 kb ?
8 mStrawberry(708 bp) pSB1C3 2,0 kb 1,4 kb ?
9 DREB1C promoter(463 bp) pSB1C3 2,5 kb probably only one cut -> one NotI site mutated
10 Laccase(1587 bp) pSB1C3 2,0 kb 1,3 kb ?
11 SV40(419 bp) pSB1C3 2,0 kb 1,6 kb this could be the laccase
12 cjBlue(696 bp) pSB1C3 2,0 kb 0,5 kb ?
  • Gel 1, Row 2:
lane part plasmid band 1 band 2 result
2 alcA (843 bp) pSB1C3 2,0 kb 0,7 kb ?
3 eforRed (681 bp) pSB1C3 plasmid plasmid bands (coiled, supercoiled, etc.)
4 amilGFP (699 bp) pSB1C3 2,0 kb 0,7 kb right part
5 mCFP (714 bp) pSB1C3 2,0 kb 0,7 kb right part
6 RD29A promoter (1535 bp) pSB1C3 2,0 kb 1,5 kb right part
7 amilCP (669 bp) pSB1C3 2,0 kb 0,7 kb right part
8 CMV promoter (580 bp) pSB1C3 2,0 kb 0,6 kb right part
9 middle linker (24 bp) pMA-BBFR 2,4 kb short insert went through the gel
10 GSAT (108 bp) pMA-BBFR 2,4 kb 0,1 kb right part
11 GFP(720 bp) pSB1A2 ?
12 long linker (36 bp) pMA-BBFR 2,4 kb short insert went through the gel
  • Gel 2:
lane part plasmid band 1 band 2 result
2 SEG linker (108 bp) pMA-BBFR 2,4 kb short insert went through the gel
3 short linker (12 bp) pMA-BBFR 2,4 kb short insert went through the gel
4 FluA (522 bp) pMA-BBFR 2,4 kb 0,5 kb right part
5 mCherry (769 bp) pSB2K3 4,4 kb 0,75 kb right part
6 Cerulean (778 bp) pSB2K3 ?
7 mRFP1 (706 bp) pSB2K3 4,4 kb 0,7 kb right part
8 mOrange (769 bp) pSB2K3 4,4 kb 0,75 kb right part
9 PIF3-20aa (366 bp) pSB1C3 2,0 kb 0,35 kb right part
10 20aa-PIF3 (366 bp) pSB1C3 2,0 kb 0,35 kb two plasmids and two insert can be seen
11 LexA (ca. 6 kb) pSB1C3 > 8 kb only one cut, huge plasmid

Picking of Plasmid P23 (CaMV35S) and Ligation Product F8 + F15 (TEV)

Investigator: Jeff, Florian

Aim of the study: Picking of Plasmid P23 (CaMV35S) and Ligation Product F8 + F15 (TEV) for Miniprep.

Operational sequence:

  • Picking and overnight culture after standard laboratory's protocol. (CamR LB-medium)
  • 1 colony of P23 were picked.
  • 7 colonies of F8 + F15 were picked.

Sequencing of P63 & P64

Investigators: Louise

Aim of the experiment: Sequencing of genes for which no prior sequencing results were available.

Procedure: The DNA was prepared for sequencing according to the Eurofins SmartSeq Kit protocol (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer).

The different genes we sequenced received the following barcodes:

Label Name Barcode1 Barcode2
p63 EreA FR01002349 FR01002350
p64 EreA FR01002351 FR01002352

Wednesday, May 15th

Preparative digestion of psB1C3-RFP-generator (P60) and another psB1C3 (P8) as well as P64 (EreA in defect psB1C3 (F8)) with XbaI & AgeI

Investigator: Louise,Leonie,Johanna

Aim of the experiment:Preparative digestion of psB1C3-RFP-generator (P60) and another psB1C3 (P8) as well as P64 (EreA in defect psB1C3 (F8)) with XbaI & AgeI to recover EreA and prepare two new vectors for cloning.

Procedure:

  • Batch for preparative digestion of PCR product and EreB (F2) with XbaI & AgeI.
volume reagent
20 µl Plasmid (P8,P60,P64)
4 µl NEBuffer 4
0.4 µl BSA (100x)
1 µl AgeI-HF
1 µl XbaI
13.6 µl ddH2O
=40 µl TOTAL
  • Incubation for 2.5 h at 37 °C
  • The digested fragments were labelled F17(P8), F18(P60), F19(P64)

PCR, purification and analytical geleletrophoresis of and EreB (P16)

Investigator: Jeff, Louise

Aim of the experiment: PCR of EreB (P16).

Procedure:

Operational sequence:

  • PCR reaction mixture
volume reagent
10 µl 5x OneTaq Standard Reaction Buffer
1 µl 10 mM dNTPs
1 µl 10 µM Forward Primer (O31 (EreB_for))
1 µl 10 µM Reverse Primer (O32 (EreB_rev))
0.25 µL OneTaq Hot Start DNA Polymerase (Finally: 1.25 units/50 µL)
1 µl Plasmid DNA (P15; P16)
35.75 µL ddH2O Water
=50 µL TOTAL
  • Mix with pipette
  • The PCR program TMKS was performed after following scheme:
Initial denaturation 94 °C 30 s
30 cycles 94 °C 30 s
52 °C 60 s
68 °C 80 s
Final extension 68 °C 5 min
Hold 4 °C infinite
  • After PCR, the product was purified with QIAquick PCR Purification Kit, Qiagen.
  • 4 µl of the purified PCR products were mixed with 0.4 µl DNA loading buffer (10x) for analytical gelelectrophoresis
  • Analytical gelelectrophoresis was performed at 90 V for 30 min in 1% agarose gel.
1 kbp ladder F16
Fragment-size like expected

TUM13 20130515 PCR P16.png

Purification and ligation of digested products F17, F18, F19

Investigator: Jeff, Louise

Aim of the experiment: Purification and ligation of digested products F17, F18, F19.

Procedure:

  • To purify the digested Fragments the QIAquick PCR Purification Kit was used. The concentration of the purified product was found to be XX ng/µl via Nano drop.

Ligation of F19 + FXX(pSB1C3)

  • Ligation batch for F19+FXX (positive control)
volume reagent
1.35 µl F8 (74.3 ng/µl, 2086 bp)
X µl F14 (5 ng/µl, 1257 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
=20 µl TOTAL
  • Negative control was also prepared. Instead of the insert, the same volume of ddH2O was added to the reaction batch.
  • Cycled ligation has been performed after following protocol in a thermocycler:
99 cycles 12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
Hold 16 °C infinite

Analytical digestion and analytical gelelectrophoresis of P90-P97 (TEV protease, XbaI+AgeI) and P97 (CaMV p35S, XbaI+PstI)

Investigator: Jeff

Aim of the experiment: Analytical digestion and analytical gelelectrophoresis of P90-P97 (TEV protease, XbaI+AgeI) and P97 (CaMV p35S, XbaI+PstI).

Procedure:

  • Mastermix for analytical digestion of P90-P96 with XbaI+AgeI-HF:
volume reagent
16 µl NEBuffer 4 (10x)
1.6 µl BSA (100x)
2 µl XbaI (20 U/µl)
2 µl AgeI-HF (20 U/µl)
118.4 µl ddH2O
=140 µl TOTAL
  • Batch for digestion of P90-P96 with XbaI+AgeI-HF:
volume reagent
2.5 µl Plasmid DNA
17.5 µl Mastermix
=20 µl TOTAL
  • Batch for digestion of P90-P96 with XbaI+AgeI-HF:
volume reagent
2.5 µl Plasmid DNA
2 µl NEBuffer 4 (10x)
0.2 µl BSA (100x)
0.25 µl XbaI (20 U/µl)
0.25 µl AgeI-HF (20 U/µl)
14.8 µl ddH2O
=20 µl TOTAL
  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed at 90 V for 60 min.

Results:

1 kbp ladder DNA ladder Digestion of P90 Digestion of P91 Digestion of P92 Digestion of P93 Digestion of P94 Digestion of P95 Digestion of P96 Digestion of P97
Insert has expected length Insert has expected length Insert has expected length Insert has expected length Corrupt Insert has expected length Insert has expected length Corrupt
  • The inserts for TEV semm to be right in the most cases, but the backbone has mutated and it should be cloned into a new pSB1C3 with new same restriction enzymes (XbaI+AgeI)!
  • The forward sequencing of CaMV p35S is right but the analytical digestion is wrong. Maybe further parts are downstream of the promoter?! Reverse sequencing should be performed for further analysis.

TUM13 20130515 P90-P96 XbaI.png

Thursday, May 16th

Preparative digestion of pSH21 (P61), psB1A2(P41) and P96 (TEV S19V)

Investigator: Jeff, Katrin

Aim of the experiment: Preparative digestion of pSH21 (P61)and psB1A2(P41) with EcoRI and P96 (TEV S19V) with XbaI & AgeI for subsequent ligation.

Procedure:

  • Batch for preparative digestion of pSH21 with EcoRI
volume reagent
20 µl Plasmid DNA P61
4 µl Buffer 4(10x)
1 µl EcoRI (20 U/µl)
15 µl ddH2O
=40 µl TOTAL
  • Batch for preparative digestion of psB1A2 with EcoRI
volume reagent
20 µl Plasmid DNA P41
4 µl Buffer 4(10x)
1 µl EcoRI (20 U/µl)
15 µl ddH2O
=40 µl TOTAL
  • Batch for preparative digestion of P96 (TEV S219V) with XbaI & AgeI.
volume reagent
20 µl Plasmid DNA P96
4 µl Buffer 4(10x)
1 µl XbaI (20 U/µl)
1 µl AgeI-HF (20 U/µl)
13.6 µl ddH2O
=40 µl TOTAL
  • Incubation for 3 h at 37 °C.
  • The resulting fragments were named: F23 (P41) and F22 (P61)
  • 4 µl of DNA loading buffer (10x) were added to the reaction batch containing pSH21 (P61) after digestion and were loaded on an 1% agarose gel for preparative gelelectrophoresis.
  • Preparative gelelectrophoresis was performed at 70 V for 90 min.
1 kbp ladder P61 digestion = F23
Fragment-size like expected; band was cut out

TUM13 20130516 P96 XbaI.AgeI P61 EcoRI.png

  • The band had the expected length. They were cut out and purified using the QIAquick Gel Extraction Kit, QIAGEN

Preparative digestion of ereB (P64) with XbaI & AgeI.

Investigator: Jeff, Louise, Katrin

Aim of the experiment:Preparative digestion of EreB (P64) with XbaI & AgeI.

Procedure:

  • Batch for preparative digestion of PCR product and EreB (F2) with XbaI & AgeI.
volume reagent
20 µl Plasmid
4 µl NEBuffer 4
0.4 µl BSA (100x)
1 µl AgeI-HF
1 µl XbaI
13.6 µl ddH2O
=40 µl TOTAL
  • Incubation for 2.5 h at 37 °C
  • The digested fragments were labelled

Dephosphorylation of F23

Investigator: Jeff, Katrin

Aim of the experiment: Dephosphorylation of cut vector psB1A2 to prevent re-ligation

Procedure:

  • the digestion product was purified with QIAquick PCR Purification Kit, Qiagen in order to change the buffer
  • Batch for the dephosphorylation of F23
volume reagent
30 µl Plasmid DNA F23 (2 µg)
4 µl 10X Fast AP buffer
2 µl FastAP Thermosensitive Alkaline

Phosphatase

4 µl ddH2O
=40 µl TOTAL
  • the reaction batch was spun briefly and incubated at 37 °C for 10 minutes
  • the reaction was stopped by heating to 75 °C for 5 minutes

Ligation of pSH21 (F22) with psB1A2(F23), TEV (P96), EreA (P64), pSB1A2(P41)

Investigator: Jeff, Katrin

Aim of the experiment: ligation of pSH21 (F22) with pSB1A2(F23), TEV (F20) with pSB1C3 (F17), EreA (F19)with pSB1C3 (F17) and EreB (F21) with pSB1C3 (F17)

Procedure:

  • Ligation batch for EreB (F21) with pSB1C3 (F17)
volume reagent
1.6 µl F17 (61,4 ng/µl)
15,4  µl F21 (8,3 ng/µl)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
=20 µl TOTAL


  • Ligation batch for TEV (F20) with pSB1C3 (F17)
volume reagent
1.6 µl F17 (61,4 ng/µl)
4,1  µl F20 (24,7  ng/µl)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
11,3 µl ddH20
=20 µl TOTAL
  • Ligation batch for pSH21 (F22) with pSB1A2(F23)
volume reagent
0,85  µl F23 (118,1 ng/µl)
2,3  µl F22 (119,0  ng/µl)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
13,85 µl ddH20
=20 µl TOTAL
  • Ligation batch for EreA (F19) with pSB1C3 (F17)
volume reagent
1.6 µl F17 (61,4 ng/µl)
6,4  µl F19 (8,3 ng/µl)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
9  µl ddH20
=20 µl TOTAL


  • Negative control was also prepared. Instead of the insert, the same volume of ddH2O was added to the reaction batch.
  • the ligation was performed at 16 °C overnight

Friday, May 17th

Transformation of E. coli XL1 blue with F17+F19, F17+F20, F17+F21, F22+F23, F17 (negative control), F23 (negative control)

Investigator: Jeff, Katrin

Aim of the experiment: Transformation of ligation products F17+F21 (pSB1C3, EreB), F17+F20 (pSB1C3, TEV), F17+F19 (pSB1C3, EreA), F23+F22 (pSB1A2, pSH21) and negative controls

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 5 µl of DNA was added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on chloramphenicol plates (F17+F19, F17+F20, F17+F21, F17 negative) or ampicillin plates (F23+F22, F23 negative control)
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was discarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on chloramphenicol plates (F17+F19, F17+F20, F17+F21) or ampicillin plates (F23+F22)

Quick Change mutagenesis to remove mutations found by sequencing in our gene constructs

Investigator: Jeff, Leonie

Aim of the experiment: removal of forbidden restiction sites from laccase

Operational sequence

PCR general setup

volume reagent
5 µl 10x Pfu Ultra II buffer
1 µl DNA template (p28)
0,5 µl each 1:10 dilution of appropriate Oligos (1: O26 + O27, 2: O28 + O29, 3: O30 + O31, 4: O32 + O33 )
42 µl ddH2O
1 µl dNTP mix
1 µl Pfu Ultra II DNA polymerase (2.5 U / µl)


PCR cycling parameters

Segment Cycles Temperature Time
1 1 95 °C 30 sec
2 12 95 °C 30 s
55 °C 1 min
68 °C 4 min
3 1 4 °C hold

Transformation of E. coli XL1 blue with the 4 Quickchangeproducts using 1: O26 + O27, 2: O28 + O29, 3: O30 + O31, 4: O32 + O33

Investigator: Jeff, Andi, Johanna, Leonie

Aim of the experiment: Transformation of E. coli XL1 blue with the 4 Quickchangeproducts using 1: O26 + O27, 2: O28 + O29, 3: O30 + O31, 4: O32 + O33

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 5 µl of DNA was added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on chloramphenicol plates 1: O26 + O27, 2: O28 + O29, 3: O30 + O31, 4: O32 + O33
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was discarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on chloramphenicol plates (1: O26 + O27, 2: O28 + O29, 3: O30 + O31, 4: O32 + O33)

Saturday, May 18th

Picking of transformed Plasmid E. coli XL1 blue with F17+F19, F17+F20, F17+F21, F22+F23

Investigator: Andi, Jeff

Aim of the study: Picking of transformed Plasmid F17+F19, F17+F20, F17+F21, F22+F23 .

Operational sequence:

  • Picking and overnight culture after standard laboratory's protocol. (CamR/AmpR LB-medium)
  • 2 colonies were picked for every Transformation product.

Sunday, May 19th

Miniprep of overnight culture of transformated E. coli XL1 blue with F17+F19, F17+F20, F17+F21, F22+F23

Investigator: Jeff, Andi

Aim of the experiment: Miniprep of overnight culture of transformated E. coli XL1 blue with F17+F19, F17+F20, F17+F21, F22+F23 of 2 clones picked the day before

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)

Analytical digestion and analytical gelelectrophoresis of F17+F19, F17+F20, F17+F21 and F22+F23

Investigator: Jeff, Andi

Aim of the experiment: Analytical digestion and analytical gelelectrophoresis of ligation products F17+F19, F17+F20, F17+F21, F22+F23.

Procedure:

  • Mastermix for analytical digestion of F17+F19, F17+F20, F17+F21 with XbaI+PstI-HF:
volume reagent
14 µl NEBuffer 4 (10x)
1.4 µl BSA (100x)
1.75 µl XbaI (20 U/µl)
1.75 µl AgeI-HF (20 U/µl)
103.6 µl ddH2O
=122.5 µl TOTAL
  • Batch for digestion of F22+F23 with EcoRI-HF:
volume reagent
2.5 µl Plasmid DNA
2 µl NEBuffer 4 (10x)
15.25 µl ddH2O
0.25 µl EcoRI-HF (20 U/µl)
=20 µl TOTAL
  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed two times for each ligation product at 90 V for 60 min.

Results:

1 kbp ladder DNA ladder Digestion of F17+F19 Digestion of F17+F19 Digestion of F17+F20 Digestion of F17+F20 Digestion of F17+F21 Digestion of F17+F21 Digestion of F22+F23 Digestion of F22+F23
Insert has expected length Insert has expected length, the first line represents the rest of the uncut Plasmid Insert has expected length Insert has expected length, the first line represents the rest of the uncut Plasmid Insert has expected length Insert has expected length Insert has expected length, insert and cut Plasmid overlay each other, because of the same length Corrupt

TUM13 20130519 P98-P103 XbaI.PstI P104-P105 EcoRI(1).png

Quick Change mutagenesis to remove forbidden restriction sites of P28 (Laccase), P100 (TEV S219V), P102 (EreB)

Investigator: Jeff, Andi

Aim of the experiment: Removal of forbidden restiction sites from P28 (Laccase), P100 (TEV S219V), P102 (EreB).

Operational sequence

PCR general setup

Procedure:

PCR

Reaction batch 1

volume reagent
2.5 µl 10x Pfu Ultra II buffer
4 µl Plasmid template (P28/P100/P102)
1 µl 1:10 dilution of O26 (for P28, 10 µM)/O16 (for P102, 10 µM)/O36 (for P100, 10 µM)
16.5 µl ddH2O
0.5 µl dNTP mix
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)

Reaction batch 2

volume reagent
2.5 µl 10x Pfu Ultra II buffer
4 µl Plasmid P38 template
1 µl 1:10 dilution of O27 (for P28, 10 µM)/O17 (for P102, 10 µM)/O37 (for P100, 10 µM)
16.5 µl ddH2O
0.5 µl dNTP mix
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)

PCR cycling parameters

Segment Cycles Temperature Time
1 1 95 °C 30 s
2 10 95 °C 30 s
55 °C 1 min
68 °C 4 min
  • Having completed the PCR cycling parameters listed above both PCR reaction batches were mixed together and the cycling parameters listed above were one time more applied, but the amount of cycles have been increased to 20.
  • Digestion of the parental DNA with DpnI: Addition of 1 µl DpnI to the reaction batch and incubate for 1 h at 37 °C.

Analytical gelelectrophoresis of QuickChange products of P100, P102 and P28 to check whether the QuickChange PCR and DpnI digestion were successful

Investigator:

Aim of the experiment:

Procedure:

TUM13 20130519 P28QC P100QC P102QC.png

Transformation of the Quickchange products with P28, P100 and P102 into E. coli XL1 blue

Investigator: Jeff, Andi

Aim of the experiment: Transformation of E. coli XL1 blue with P28, P102 and P100.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 2 µl of DNA was added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

Week 5

Tuesday, May 21st

Quick Change mutagenesis to remove forbidden restriction sites - SDMI - of P28 (Laccase), P100 (TEV S219V), P102 (EreB)

Investigator: Jeff, Andi, Johanna

Aim of the experiment: Removal of forbidden restiction sites from P28 (Laccase), P100 (TEV S219V), P102 (EreB).

Operational sequence

PCR general setup

Procedure:

PCR

Reaction batch 1

volume reagent
2.5 µl 10x Pfu Ultra II buffer
4 µl Plasmid template (P28/P100/P102)
1 µl 1:10 dilution of O26 (for P28, 10 µM)/O16 (for P102, 10 µM)/O36 (for P100, 10 µM)
16.5 µl ddH2O
0.5 µl dNTP mix
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)

Reaction batch 2

volume reagent
2.5 µl 10x Pfu Ultra II buffer
4 µl Plasmid P38 template
1 µl 1:10 dilution of O27 (for P28, 10 µM)/O17 (for P102, 10 µM)/O37 (for P100, 10 µM)
16.5 µl ddH2O
0.5 µl dNTP mix
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)

PCR cycling parameters

Segment Cycles Temperature Time
1 1 95 °C 30 s
2 10 95 °C 30 s
55 °C 1 min
68 °C 4 min
  • Having completed the PCR cycling parameters listed above both PCR reaction batches were mixed together and the cycling parameters listed above were one time more applied, but the amount of cycles have been increased to 20.
  • Digestion of the parental DNA with DpnI: Addition of 1 µl DpnI to the reaction batch and incubate for 1 h at 37 °C.

Analytical gelelectrophoresis of QuickChange products of P100, P102 and P28 to check whether the QuickChange PCR and DpnI digestion were successful

Investigator:

Aim of the experiment:

Procedure:

TUM13 20130521 P28QC P100QC P102QC.png

Transformation of the Quickchange products with P28, P100 and P102 into E. coli XL1 blue

Investigator: Jeff, Andi, Johanna

Aim of the experiment: Transformation of E. coli XL1 blue with P28, P102 and P100.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 2 µl of DNA was added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

Sequencing of P105, P28, P100, P102 & P98

Investigators: Jeff, Andi,Johanna

Aim of the experiment: Sequencing of genes for which no prior sequencing results were available.

Procedure: The DNA was prepared for sequencing according to the Eurofins SmartSeq Kit protocol (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer).

The different genes we sequenced received the following barcodes:

Label Name Barcode1 Barcode2
p105 IRES FR01002288 FR01002269
p102 EreB FR01002270 FR01002275
p100 TEV S219V FR01002278 FR01002279
p98 EreA FR01002276 FR01002277
p28 Laccase FR01002280

Preparation of Knop-Medium for Moss

Investigator: Jeff, Andi, Johanna, Rosario

Aim of the experiment: Preparation of Knop-Medium for Moss

Procedure:

  • All four prepared stocks have been: 25g/L KH2PO4; 25g/L KCl; 25g/L MgSO4 x 7 H2O; 100g/L Ca(NO3)2
  • Volume of prepared Medium: 1L
  • 10 ml of each stock were converted into a 1,8L Erlenmeyer flask and filled up to 1L with destilled water (ELGA); 12,5mg FeSO4 x 7 H2O were added; the pH was set to 5.8 with KOH
  • The prepared Volume of 1L was shared equally to 500ml Erlenmeyer flasks, so each Erlenmeyer flask contained 200 ml of the Knop-Medium
  • All flasks have been autoclaved

Picking of transformed Plasmid E. coli XL1 blue with QuickChange products of P100 (TEV, QC with O36/O37) and P102 (EreB, QC with O16/O17)

Investigator: Andi, Jeff, Johanna, Rosario

Aim of the study: Picking of transformed Plasmid E. coli XL1 blue with QuickChange products of P100 (TEV, QC with O36/O37) and P102 (EreB, QC with O16/O17) from Sunday, May 19th.

Operational sequence:

  • Picking and overnight culture after standard laboratory's protocol. (CamR LB-medium)
  • 3 colonies for P100QC (TEV, QC with O36/O37) and 5 colonies from P102QC (EreB, QC with O16/O17) were picked from the plates.

Wednesday, May 22nd

Miniprep of overnight culture of transformated E. coli XL1 blue with QuickChange products of P100 (TEV, QC with O36/O37) and P102 (EreB, QC with O16/O17)

Investigator: Jeff

Aim of the experiment: Miniprep of overnight culture of transformated E. coli XL1 blue with QuickChange products of P100 (TEV, QC with O36/O37) and P102 (EreB, QC with O16/O17).

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)

Picking of transformed Plasmid E. coli XL1 blue with QuickChange products of P28 (Laccase, QC with O26/O27)

Investigator: Jeff

Aim of the study: Picking of transformed Plasmid E. coli XL1 blue with QuickChange products of P28 (Laccase, QC with O26/O27).

Operational sequence:

  • Picking and overnight culture after standard laboratory's protocol. (CamR LB-medium)
  • 8 colonies for P28QC (Laccase, QC with O26/O27) were picked from the plates.

Analytical digestion and analytical gelelectrophoresis of P106, P107, P108, P109, P110, P111, P112, P113

Investigator: Jeff, Rosario, Leonie

Aim of the experiment: Analytical digestion and analytical gelelectrophoresis of Quickchanges to check whether the transformation of E. coli Xl1 Blue with QuickChanges products of P100 (TEV, QC with O36/O37: P111, P112, P113) and P102 (EreB, QC with O16/O17: P106, P107, P108, P109, P110) were successful

Procedure:
Mastermix for analytical digestion of P106, P107, P108, P109, P110, P111, P112, P113 with AgeI-HF and XbaI:

volume reagent
20 µl NEBuffer 4 (10x)
2 µl BSA (100x)
2.5 µl AgeI-HF (20 U/µl)
2.5 µl XbaI
148 µl ddH2O
= 175 µl TOTAL
  • 17,5 µl Mastermix with 2,5 µl Plasmid


Mastermix for analytical digestion of P111, P112, P113 with XbaI and SpeI and P106, P107, P108, P109, P110 with XbaI and PstI-HF:

volume reagent
20 µl NEBuffer 4 (10x)
2 µl BSA (100x)
2.5 µl XbaI
148 µl ddH2O
= 172,5 µl TOTAL
  • 17,25 µl Mastermix with 2,5 µl Plasmid and 0,25 µl SpeI or PstI respectively


Mastermix for analytical digestion of with P106, P107, P108, P109, P110 EcoRI and SpeI:

volume reagent
12 µl NEBuffer 4 (10x)
1,2 µl BSA (100x)
1,5 µl EcoRI-HF
1,5 µl SpeI-HF
88.8 µl ddH2O
= 105 µl TOTAL
  • 17,5 µl Mastermix with 2,5 µl Plasmid


Mastermix for analytical digestion of with P106, P107, P108, P109, P110 XbaI and SpeI:

volume reagent
12 µl NEBuffer 4 (10x)
1,2 µl BSA (100x)
1,5 µl XbaI
1,5 µl SpeI-HF
88.8 µl ddH2O
= 105 µl TOTAL
  • 17,5 µl Mastermix with 2,5 µl Plasmid


  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed at 90 V for 60 min.


Results:
TUM13 20130522 P111-P113 XbaI.AgeI P111-P113 XbaI.SpeI.png

1 kbp ladder DNA ladder P111 XbaI + AgeI P112 XbaI + AgeI P113 XbaI + AgeI P111 XbaI + SpeI P112 XbaI + SpeI P113 XbaI + SpeI
Ctrl Ctrl Ctrl QC succesful QC failed QC succesful


TUM13 20130522 P106-P110 XbaI.AgeI P106-P110 XbaI.PstI.png

1 kbp ladder DNA ladder P106 XbaI + AgeI P107 XbaI + AgeI P108 XbaI + AgeI P109 XbaI + AgeI P110 XbaI + AgeI P106 XbaI + PstI P107 XbaI + PstI P108 XbaI + PstI P109 XbaI + PstI P110 XbaI + PstI
Ctrl Ctrl Ctrl Ctrl Ctrl PstI inside as should be; useless experiment PstI inside as should be; useless experiment PstI inside as should be; useless experiment PstI inside as should be; useless experiment PstI inside as should be; useless experiment


TUM13 20130522 P106-P110 XbaI.SpeI P106-P110 EcoRI.SpeI.png

1 kbp ladder DNA ladder P106 XbaI + SpeI P107 XbaI + SpeI P108 XbaI + SpeI P109 XbaI + SpeI P110 XbaI + SpeI P106 EcoRI + SpeI P107 EcoRI + SpeI P108 EcoRI + SpeI P109 EcoRI + SpeI P110 EcoRI + SpeI
Ctrl Ctrl Ctrl Ctrl Ctrl QC succesful QC succesful QC succesful QC succesful QC failed

Thursday, May 23rd

Sequencing of P111, P113 and P109 (?)

Investigator: Jeff

Aim of the experiment: Sequencing of P111, P113 and P109 to check whether the QuickChange brought further unwanted mutations.

Procedure:

PCR of P111 (TEV S219V, SpeI-less) to generate Split-TEV

Investigator: Jeff

Aim of the experiment: PCR of P111 (TEV S219V, SpeI-less) to generate Split-TEV. To generate N-TEV, the primer O38 and O39 were used. To generate C-TEV, the primer O40 and O41 were used.

Procedure:

Operational sequence:

  • PCR reaction mixture
volume reagent
10 µl 5x OneTaq Standard Reaction Buffer
1 µl 10 mM dNTPs
1 µl 10 µM Forward Primer (O38 (N_Split_TEV_fw) for generating N-TEV; O40 (C_Split_TEV_fw) for generating C-TEV)
1 µl 10 µM Reverse Primer (O39 (N_Split_TEV_rv) for generating N-TEV; O41 (C_Split_TEV_rv) for generating C-TEV)
0.25 µL OneTaq Hot Start DNA Polymerase (Finally: 1.25 units/50 µL)
1 µl Plasmid DNA (P111)
35.75 µL ddH2O Water
=50 µL TOTAL
  • Mix with pipette
  • The PCR program was performed after following scheme with following conditions:
Initial denaturation 94 °C 30 s
30 cycles 94 °C 30 s
51 °C 60 s
68 °C 30 s
Final extension 68 °C 5 min
Hold 4 °C infinite
  • After PCR, the product was purified with QIAquick PCR Purification Kit, Qiagen.
  • Resulting product was labeled as F24 (N-TEV) and F25 (C-TEV).

Analytical gelelectrophoresis of F24 and F25 (N-TEV and C-TEV)

Investigator: Jeff, Rosario

Aim of the experiment: Analytical gelelectrophoresis of F24 and F25 (N-TEV and C-TEV) to check whether PCR has worked.

Procedure:

  • 4 µl of F24 and F25 were mixed with seperately with 0.44 µl of DNA loading buffer (10x) and analytical gelelectrophoresis was performed at 1% agarose gel for 60 min at 90 V.

TUM13 20130523 F24 F25.png

  • PCR products has expected length, but there are unspecific products. So we have to be cautious and have to check if we ligate the right products.

Preparative digestion of PCR products (N-TEV and C-TEV) of P111 (TEV S219V, SpeI-less) with XbaI & AgeI

Investigator: Jeff, Rosario

Aim of the experiment: Preparative digestion of PCR products (N-TEV and C-TEV) of P111 (TEV S219V, SpeI-less) with XbaI & AgeI to clone it into pSB1C3.

Procedure:

  • Batch for preparative digestion of PCR products (N-TEV and C-TEV) of P111 (TEV S219V, SpeI-less) with XbaI & AgeI.
volume reagent
25 µl PCR product F24/F25
5 µl NEBuffer 4
0.5 µl BSA (100x)
1 µl AgeI-HF
1 µl XbaI
17.5 µl ddH2O
=50 µl TOTAL
  • Incubation for 150 min at 37 °C.
  • Digested products were purified with QIAquick PCR Purification Kit, QIAGEN.
  • The digested fragments were labelled F26 (digestion of F24 with XbaI&AgeI) and F27 (digestion of F25 with XbaI&AgeI)

Ligation of F17+F26 (N-TEV in pSB1C3) and F17+F27 (C-TEV in pSB1C3)

Investigator: Jeff, Rosario

Aim of the experiment: Ligation of F17+F26 (N-TEV in pSB1C3) and F17+F27 (C-TEV in pSB1C3).

Procedure:

  • Ligation batch for F17+F26:
volume reagent
1.63 µl F17 (61.4 ng/µl, 2086 bp)
3.20 µl F26 (15.9 ng/µl, 354 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
12.17 µl ddH2O
=20 µl TOTAL
  • Ligation batch for F17+F27 (positive control)
volume reagent
1.63 µl F17 (61.4 ng/µl, 2086 bp)
2.41 µl F27 (21.1 ng/µl, 354 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
12.96 µl ddH2O
=20 µl TOTAL
  • Negative control was also prepared. Instead of the insert, the same volume of ddH2O was added to the reaction batch.
  • Cycled ligation has been performed after following protocol in a thermocycler:
99 cycles 12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
Hold 16 °C infinite
  • Lid temperature = 37 °C

Miniprep of overnight culture of transformated E. coli XL1 blue with the first Quickchange (SDMI) Product of P28

Investigator: Jeff, Andi, Rosario, Johanna, Leonie

Aim of the experiment: Miniprep of overnight culture of transformated E. coli XL1 blue with the first Quickchange Product of P28. 8 clones were picked the day before.

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)

Analytical digestion and analytical gelelectrophoresis of P28, P117, P118, P119, P120, P121, P122, P123

Investigator: Rosario, Andi, Leonie, Johanna, Jeff

Aim of the experiment: Analytical digestion and analytical gelelectrophoresis of ligation products P28, P117, P118, P119, P120, P121, P122, P123.

Procedure:

  • Mastermix for analytical digestion of P28, P117, P118, P119, P120, P121, P122, P123 AgeI-HF:
volume reagent
20 µl NEBuffer 4 (10x)
2 µl BSA (100x)
2.5 µl AgeI-HF (20 U/µl)
150.5 µl ddH2O
=175 µl TOTAL
  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed two times for each ligation product at 90 V for 60 min.

Results:

1 kbp ladder DNA ladder Digestion of P28 Digestion of P116 Digestion of P117 Digestion of P118 Digestion of P119 Digestion of P120 Digestion of P121 Digestion of P122 Digestion of P122
to be announced to be announced to be announced to be announced to be announced to be announced to be announced to be announced to be announced

Quick Change mutagenesis to remove forbidden restriction sites - SDMII - of P28 (Laccase), P106 (EreB)

Investigator: Jeff, Andi, Johanna, Rosario, Leonie

Aim of the experiment: Removal of forbidden restiction sites from P28 (Laccase), P106 (EreB).

Procedure: Quickchange - PCR

Reaction batch - P106

volume reagent Additional information
5 µl 10x Pfu Ultra II buffer
2 µl Plasmid template (P106 - 1:10 dilution) need to get to 50 ng/µl
1.25 µl 1:10 dilution of O18 (for P106, 10 µM)
1.25 µl 1:10 dilution of O19 (for P106, 10 µM)
38.5 µl ddH2O
1 µl dNTP mix
1 µl Pfu Ultra II DNA polymerase (2.5 U / µl)


PCR cycling parameters - P106

Segment Cycles Temperature Time
1 1 95 °C 30 s
2 18 95 °C 30 s
52 °C 1 min
68 °C 4 min
  • Digestion of the parental DNA with DpnI: Addition of 1 µl DpnI to the reaction batch and incubate for 1 h at 37 °C.


Reaction batch - P116 (Laccase)

volume reagent Additional information
5 µl 10x Pfu Ultra II buffer
2 µl Plasmid template - 1:5 dilution need to get to 50 ng/µl
1.25 µl 1:10 dilution of O28 for P116
1.25 µl 1:10 dilution of O29 for P116
38.5 µl ddH2O
1 µl dNTP mix
1 µl Pfu Ultra II DNA polymerase (2.5 U / µl)


PCR cycling parameters - P116

Segment Cycles Temperature Time
1 1 95 °C 30 s
2 18 95 °C 30 s
52 °C 1 min
68 °C 4 min
  • Digestion of the parental DNA with DpnI: Addition of 1 µl DpnI to the reaction batch and incubate for 1 h at 37 °C.

Transformation of the Quickchange products with P28, P100 and P102 into E. coli XL1 blue

Investigator: Jeff, Andi, Johanna, Rosario

Aim of the experiment: Transformation of E. coli XL1 blue with Quickchangeproduct SDM II of P106 and P116.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 2 µl of DNA was added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

Friday, May 24th

Transformation of E. coli XL1 blue with ligation products F17+F26 (N-TEV S219V in pSB1C3) and F17+F27 (C-TEV S219V in pSB1C3)

Investigator: Jeff, Florian

Aim of the experiment: Transformation of E. coli XL1 blue with ligation products F17+F26 (N-TEV S219V in pSB1C3) and F17+F27 (C-TEV S219V in pSB1C3).

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 10 µl of DNA was added to 200 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellets were resuspended in 100 µl of LB-medium and these concentrated cell suspensions was plated again on a new chlorampenicol plates.

Quick Change mutagenesis to remove forbidden restriction sites - SDMII - of P116 (Laccase), P109 (EreB)

Investigator: Volker, Louise, Katrin, Leonie, Flo

Aim of the experiment: Removal of forbidden restiction sites from P116 (Laccase), P109 (EreB).

Procedure: Quickchange - PCR

Reaction batch - P109

volume reagent Additional information
2.5 µl 10x Pfu Ultra II buffer
1 µl Plasmid template (P109 - 1:10 dilution) need to get to 50 ng/µl
1 µl 1:10 dilution of O18 (for P109, 10 µM)
1 µl 1:10 dilution of O19 (for P109, 10 µM)
18 µl ddH2O
1 µl dNTP mix 50mM
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)


PCR cycling parameters - P109

Segment Cycles Temperature Time
1 1 95 °C 30 s
2 21 95 °C 30 s
52 °C 1 min
68 °C 4 min 50 s
  • Digestion of the parental DNA with DpnI: Addition of 1 µl DpnI to the reaction batch and incubate for 1 h at 37 °C.


Reaction batch - P116 (Laccase)

volume reagent Additional information
2.5 µl 10x Pfu Ultra II buffer
1 µl Plasmid template - 1:5 dilution need to get to 50 ng/µl
1 µl 1:10 dilution of O28 for P116
1 µl 1:10 dilution of O29 for P116
18.0 µl ddH2O
1 µl dNTP mix 50 mM
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)


PCR cycling parameters - P116

Segment Cycles Temperature Time
1 1 95 °C 30 s
2 21 95 °C 30 s
52 °C 1 min
68 °C 4 min 50 s
  • Digestion of the parental DNA with DpnI: Addition of 1 µl DpnI to the reaction batch and incubate for 1 h at 37 °C.

Transformation of the Quickchange products into E. coli XL1 blue

Investigator: Volker

Aim of the experiment: Transformation of E. coli XL1 blue with Quickchangeproduct SDM II of P109 and P116.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 2 µl of DNA was added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

Saturday, May 25th

Analytical gelelectrophoresis of QuickChange products of P116 and P109 to check whether the QuickChange PCR and DpnI digestion were successful

Investigator: Volker, Louise, Katrin, Leonie, Flo

Aim of the experiment: Analytical gelelectrophoresis of QuickChange products of P116 and P109 to check whether the QuickChange PCR and DpnI digestion were successful

Procedure:

  • 5 µl of the PCR Quickchange products were either mixed with with 0.5 µl of DNA loading buffer (10x) and analytical gelelectrophoresis was performed at 1% agarose gel for 60 min at 90 V.


Picking of transformed Plasmid E. coli XL1 blue with QuickChange products of P116 (Laccase, QC with O28/O29) and P109 (EreB, QC with O18/O19)

Investigator: Volker

Aim of the study: Picking of transformed Plasmid E. coli XL1 blue with QuickChange products of P116 (Laccase, QC with O28/O29) and P109 (EreB, QC with O18/O19).

Procedure:

  • Picking and overnight culture after standard laboratory's protocol. (CamR LB-medium)
  • 5 colonies for P116QC (Laccase, QC with O28/O29) and 6 colonies for P109QC (EreB, QC with O18/O19) were picked from the plates.

Picking of E. coli XL1 blue with ligation products F17+F26 (N-TEV S219V in pSB1C3) and F17+F27 (C-TEV S219V in pSB1C3)

Investigator: Volker

Aim of the study: Picking of E. coli XL1 blue with ligation products F17+F26 (N-TEV S219V in pSB1C3) and F17+F27 (C-TEV S219V in pSB1C3).

Procedure:

  • Picking and overnight culture after standard laboratory's protocol. (CamR LB-medium)
  • 5 colonies were picked from plates for E. colis XL1 blue transformed with ligation products F17+F26 (N-TEV S219V in pSB1C3) and F17+F27 (C-TEV S219V in pSB1C3).

Sunday, May 26th

Miniprep of overnight cultures of transformated E. coli XL1 blue with QuickChange products of P116 (Laccase, QC with O28/O29) and P109 (EreB, QC with O18/O19)

Investigator: Katrin, Louise

Aim of the experiment: Miniprep of overnight cultures of transformated E. coli XL1 blue with QuickChange products of P116 (Laccase, QC with O28/O29) and P109 (EreB, QC with O18/O19).

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)

Analytical digestion and gelelectrophoresis to check whether the transformation of E. coli Xl1 Blue with QuickChanges products of P116 (Laccase, QC with O28/O29) and P109 (EreB, QC with O18/O19) were successful

Investigator: Katrin, Louise

Aim of the experiment:Analytical digestion and gelelectrophoresis to check whether the transformation of E. coli Xl1 Blue with QuickChanges products of P116 (Laccase, QC with O28/O29) and P109 (EreB, QC with O18/O19)

Procedure:

  • analytical digestion of Quickchange products of P109 (EreB, QC with O18/O19)
volume reagent
2 µl NEB CutSmart Buffer (10x)
0,25  µl PstI-HF (20 U/µl)
2,5 µl DNA from Miniprep
15,25 µl ddH2O
=20 µl TOTAL
  • in order to check if the QC was successful, P109 (before QC) was also digested


  • analytical digestion of Quickchange products of P116 (Laccase, QC with O28/O29)
volume reagent
2 µl NEB CutSmart Buffer (10x)
0,25 µl EcoRI-HF
0,25  µl NgoMIV
2,5 µl DNA from Miniprep
15  µl ddH2O
=20 µl TOTAL
  • in order to check if the QC was successful, P116 (before QC) was also digested
  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed at 90 V for 60 min.


TUM13 20130526 anal Verd P116 EcoRI.NgoMIV P128-P131,P124 EcoRI.NgoMIV P126,P137-P139 XbaI.AgeI.png

1 kbp ladder DNA ladder# P116 (Laccase before QCII) digested with EcoRI-HF, NgoMIV Laccase after QCII (P128) digested with EcoRI-HF, NgoMIV Laccase after QCII (P129) digested with EcoRI-HF, NgoMIV Laccase after QCII (P130) digested with EcoRI-HF, NgoMIV Laccase after QCII (P131) digested with EcoRI-HF, NgoMIV Laccase after QCII (P124) digested with EcoRI-HF, NgoMIV belongs to other experiment belongs to other experiment belongs to other experiment belongs to other experiment
as expected as expected as expected as expected as expected as expected

Laccase P124 was chosen for sequencing


TUM13 20130526 anal Verd PP127,P140-P142 XbaI.AgeI P125,P132-P136 PstI P109 PstI.png

1 kbp ladder DNA ladder belongs to other experiment belongs to other experiment belongs to other experiment belongs to other experiment EreB after QCII (P125) digested with PstI EreB after QCII (P132) digested with PstI EreB after QCII (P133) digested with PstI EreB after QCII (P134) digested with PstI EreB after QCII (P135) digested with PstI EreB after QCII (P136) digested with PstI EreB before QCII (P109) digested with PstI
as expected as expected as expected as expected as expected as expected as expected

EreB P125 was chosen for sequencing

Miniprep of ligation products of N-TEV (F17+F26) and C-TEV (F17+F25) with pSB1C3

Investigator: Katrin, Louise

Aim of the experiment: Miniprep of ligation products of N-TEV (F17+F26) and C-TEV (F17+F25) with pSB1C3

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)

Analytical digestion and gelelectrophoresis of ligation products F17 + F26, F17 + F27

Investigator: Katrin, Louise

Aim of the experiment: Analytical digestion and gelelectrophoresis to check whether the ligation of N-TEV (F17+F26) and C-TEV (F17+F25) in pSB1C3 were successful

Procedure:

  • analytical digestion of ligation products of N-TEV (F17+F26) and C-TEV (F17+F25)in pSB1C3

Mastermix:

volume reagent
22 µl NEB Buffer 4 (10x)
2,2  µl BSA (100X)
2,75 µl XbaI
2,75 µl AgeI-HF
162,8 µl ddH2O
=192,5 µl TOTAL


  • 2,5 µl of miniprep products were added to 17,5  µl Mastermix
  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed at 90 V for 60 min.


TUM13 20130526 anal Verd P116 EcoRI.NgoMIV P128-P131,P124 EcoRI.NgoMIV P126,P137-P139 XbaI.AgeI.png

1 kbp ladder DNA ladder# belongs to other experiment belongs to other experiment belongs to other experiment belongs to other experiment belongs to other experiment belongs to other experiment N-TEV ligated into pSB1C3 (F17 + F26) (P126) digested with XbaI, AgeI-HF N-TEV ligated into pSB1C3 (F17 + F26) (P137) digested with XbaI, AgeI-HF N-TEV ligated into pSB1C3 (F17 + F26) (P138) digested with XbaI, AgeI-HF N-TEV ligated into pSB1C3 (F17 + F26) (P139) digested with XbaI, AgeI-HF
as expected as expected as expected as expected

N-TEV ligated into pSB1C3 (F17 + F26) (P126) was chosen for sequencing


TUM13 20130526 anal Verd PP127,P140-P142 XbaI.AgeI P125,P132-P136 PstI P109 PstI.png

1 kbp ladder DNA ladder C-TEV ligated into pSB1C3 (F17 + F27) (P127) digested with XbaI, AgeI-HF C-TEV ligated into pSB1C3 (F17 + F27) (P140) digested with XbaI, AgeI-HF C-TEV ligated into pSB1C3 (F17 + F27) (P141) digested with XbaI, AgeI-HF C-TEV ligated into pSB1C3 (F17 + F27) (P142) digested with XbaI, AgeI-HF belongs to other experiment belongs to other experiment belongs to other experiment belongs to other experiment belongs to other experiment belongs to other experiment belongs to other experiment
as expected as expected as expected as expected

C-TEV ligated into pSB1C3 (F17 + F27) (P127) was chosen for sequencing

Sequencing of P124-P127

Investigators: Louise, Katrin

Aim of the experiment: Sequencing of QCII products (EreB, Laccase) and ligation product of split-TEV

Procedure: The DNA was prepared for sequencing according to the Eurofins SmartSeq Kit protocol (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer).

The different genes we sequenced received the following barcodes:

Label Name Barcode1 Barcode2
p124 Miniprep of transformation of QC product of P116 (Laccase, QC with O28/O29)(QC - SDMII - of Bpul Laccase to remove forbidden NgoMIV) FR01002337 (VR) FR01002338 (VF2)
p125 Miniprep of transformation of QC product of P109 (EreB, QC with O18/O19) (QC - SDMII - of EreB to remove forbidden PstI) FR01002339 (VR) FR01002340 (VF2)
p126 Miniprep of ligation product F17 + F26 (N-TEV) FR01002341 (VR) FR01002342 (VF2)
p127 Miniprep of ligation product F17 + F27 (C-TEV) FR01002343 (VR) FR01002344 (VF2)

Week 6

Monday, May 27th

Oligohybridization of MiniMCS (O56,O57) and Spytag (O54,O55)

Investigator: Leonie,Johanna

Aim of the experiment: Oligohybridization of MiniMCS (MiniMCSII_fw (O56) and MiniMCSII_rv (O57) and of Spytag (SpyTag_fw (O54) and SpyTag_rv (O55))

Operational sequence

  • 25 µL of 100 pmol/µl of MiniMCS fw and 25 µL of 100 pmol/µl MiniMCS rev in one Eppi. 25 µL of 100 pmol/µl of Spytag fw and 25 µL of 100 pmol/µl Spytag rev in a second Eppi
  • Heating up to 95 °C for 5 min
  • Cooling at RT in a styropor box overnight

PCR of npt-Kasette (P115), PIF3 (P51), pActin (P114) and t35S (P114)

Investigator: Leonie, Johanna

Aim of the experiment: PCR of npt-Kasette (P115), PIF3 (P51), pActin (P114) and t35S (P114).

Procedure:

Operational sequence:

  • PCR reaction mixture
volume reagent
10 µl 5x OneTaq Reaction GC Buffer
1 µl 10 mM dNTPs
1 µl 10 µM Forward Primer (P114:O62 (pActin_for); P114:O60 (t35S_for); P115:O58 (npt-Kasette_for); P51:O66 (PIF3_for))
1 µl 10 µM Reverse Primer (P114:O63 (pActin_rev); P114:O61 (t35S_rev); P115:O59 (npt-Kasette_rev); P51:O67 (PIF3_rev))
0.25 µL OneTaq Hot Start DNA Polymerase (Finally: 1.25 units/50 µL)
1 µl Plasmid DNA (P114; P115; P51)
35.75 µL ddH2O Water
=50 µL TOTAL
  • Mix with pipette
  • The PCR program was performed after following scheme:
Initial denaturation 94 °C 30 s
30 cycles 94 °C 30 s
49 °C 60 s
68 °C 100 s
Final extension 68 °C 5 min
Hold 4 °C infinite
  • After PCR, the product was purified with QIAquick PCR Purification Kit, Qiagen.

Results:

  • PCR did not work properly because primer concentration was wrong.

Preparative digestion and gelelectrophoresis of P45 (FluA-Psb1C3) with XbaI & AgeI, P39 with AgeI & PstI, P20 with NgoMIV & PstI

Investigator: Andi

Aim of the experiment:Preparative digestion of P45 (FluA-Psb1C3) with XbaI & AgeI, P39 with AgeI & PstI, P20 with NgoMIV & PstI to clone fragment of P45 into F17 (pSB1C3) and to fusion Middle linker of P39 with GFP of P20.

Procedure:

Batch for preparative digestion of P45 (FluA-Psb1C3) with XbaI & AgeIwith XbaI & AgeI.

volume reagent
20 µl P45
4 µl NEBuffer 4
0.4 µl BSA (100x)
2 µl AgeI-HF
2 µl XbaI
11.6 µl ddH2O
=40 µl TOTAL

Batch for preparative digestion of P39 (Middle-Linker) with PstI and AgeI.

volume reagent
20 µl P39
4 µl NEBuffer 4
0.4 µl BSA (100x)
2 µl AgeI-HF
2 µl PstI
11.6 µl ddH2O
=40 µl TOTAL

Batch for preparative digestion of P20 (GFP-Psb1C3) with NgoMIV and PstI.

volume reagent
20 µl P45
4 µl NEBuffer 4
0.4 µl BSA (100x)
2 µl NgoMIV
2 µl PstI
11.6 µl ddH2O
=40 µl TOTAL
  • Incubation for 120 min at 37 °C.
  • Preparative gelelectrophoresis was performed at 90 V for 1.5 h.

TUM13 20130527 P45 XbaI.AgeI P39 AgeI.PstI P20 NgoMIV.PstI.png

1 kbp ladder P20 digested with NgoMIV&PstI (=F30) P20 digested with NgoMIV&PstI (=F30) P39 digested with AgeI&PstI (=F29) P39 digested with AgeI&PstI (=F29) P45 digested with XbaI&AgeI (=F28) P45 digested with XbaI&AgeI (=F28)
lower band was cut out lower band was cut out band was cut out band was cut out lower band was cut out lower band was cut out
  • Bands were extracted by QIAquick Gel Extraction Kit, QIAGEN.

Quick Change mutagenesis to remove forbidden restriction sites - SDMIII - of P124(Laccase), P125 (EreB)

Investigator: Andi

Aim of the experiment: Removal of forbidden restiction sites from P124 (Laccase), P125 (EreB).

Procedure: Quickchange - PCR

Reaction batch - P124

volume reagent Additional information
2.5 µl 10x Pfu Ultra II buffer
1 µl Plasmid template (P124 - 1:6 dilution) need to get to 50 ng/µl
1 µl 1:10 dilution of O30 (for P125, 10 µM)
1 µl 1:10 dilution of O31 (for P125, 10 µM)
18 µl ddH2O
1 µl dNTP mix 50mM
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)

Reaction batch - P125

volume reagent Additional information
2.5 µl 10x Pfu Ultra II buffer
1 µl Plasmid template (P125 - 1:6 dilution) need to get to 50 ng/µl
1 µl 1:10 dilution of O20 (for P125, 10 µM)
1 µl 1:10 dilution of O21 (for P125, 10 µM)
18 µl ddH2O
1 µl dNTP mix 50mM
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)

PCR cycling parameters for both batches

Segment Cycles Temperature Time
1 1 95 °C 30 s
2 21 95 °C 30 s
52 °C 1 min
68 °C 4 min 50 s
  • Digestion of the parental DNA with DpnI: Addition of 1 µl DpnI to the reaction batch and incubate for 1 h at 37 °C.

Preparation of ordered primers

Investigators: Andi

Aim of the experiment: Dissolving of primer pallets to provide a concentration of 100 pmol/µl

Procedure: We added an amount of water which gave us a final primer concentration of 100 pmol/µl.

Primers were labeled as follows:

Label Oligonr.
O54 Spytag_fw
O55 Spytag_rev
O56 MiniMCSII_fw
O57 MiniMCSII_rev
O58 Npt_for
O59 Npt_rev
O60 t35S_for
O61 t35S_rev
O62 pACT_for
O63 pACT_rev
O64 NucA_for
O65 NucA_rev
O66 Pif3_for
O67 Pif3_rev

Transformation of P45, P51, P100 and P102 into E. coli XL1 blue

Investigator: Andi, Johanna

Aim of the experiment: Transformation of E. coli XL1 blue with P45, P51, P102 and P100.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 2 µl of DNA was added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

Picking of transformed Plasmid E. coli XL1 blue with P114, P115

Investigator: Andi

Aim of the study: Picking of transformed Plasmid E. coli XL1 blue with P114, P115.

Procedure:

  • Picking and overnight culture after standard laboratory's protocol. (AmpR LB-medium)
  • 5 colonies of P114 and P115 were picked from the plates.

Ligation of F29+F30 (GFP in pSB1C3 after middle linker, ( Gly-Gly-Ser-Gly)x2) and F17+F27 (FluA in pSB1C3)

Investigator: Jeff

Aim of the experiment: Ligation of F29+F30 (GFP in pSB1C3 after middle linker, ( Gly-Gly-Ser-Gly)x2) and F17+F27 (FluA in pSB1C3).

Procedure:

  • Ligation batch for F29+F30:
volume reagent
4.22 µl F29 (23.7 ng/µl, 2110 bp)
10.48 µl F30 (9.5 ng/µl, ~700 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
2.3 µl ddH2O
=20 µl TOTAL
  • Ligation batch for F17+F28:
volume reagent
1.63 µl F17 (61.4 ng/µl, 2086 bp)
7.8 µl F28 (9.6 ng/µl, 522 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
7.57 µl ddH2O
=20 µl TOTAL
  • Negative control was also prepared. Instead of the insert, the same volume of ddH2O was added to the reaction batch.
  • Cycled ligation has been performed after following protocol in a thermocycler:
99 cycles 12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
Hold 16 °C infinite
  • Lid temperature = 37 °C

Tuesday, May 28th

Analytical gelelectrophoresis of PCR products of P114 (O62&O63), P114 (O60&O61), P115 (O58&O59), P51 (O66&O67)

Investigator: Jeff, Rosario, Leonie

Aim of the experiment: Analytical gelelectrophoresis of PCR products of P114 (O62&O63), P114 (O60&O61), P115 (O58&O59), P51 (O66&O67).

Procedure:

  • 4 µl of PCR products of P114 (O62&O63), P114 (O60&O61), P115 (O58&O59), P51 (O66&O67) were mixed with seperately with 0.44 µl of DNA loading buffer (10x) and analytical gelelectrophoresis was performed at 1% agarose gel for 40 min at 90 V.

TUM13 20130528 PCR F33 F34 F35 F36.png

1 kbp ladder PCR products of P114 (O62&O63), P114 (O60&O61), P115 (O58&O59), P51 (O66&O67) PCR products of P114 (O60&O61) PCR products of P115 (O58&O59) PCR products of P51 (O66&O67)
PCR did work, but strong primer dimer signal PCR did work, but strong primer dimer signal PCR did not work PCR did work, but strong primer dimer signal
  • Wrong buffer (GC buffer, instead of standard reaction buffer, was used and 10x too much primers were also used)

Transformation of Quickchangeproduct SDMIII of P124 (Laccase) and P125 (EreB) + ligation product of F29+F30 + ligation product of F17+F19 into E. coli XL1 blue

Investigator: Andi, Johanna

Aim of the experiment: Transformation of Quickchangeproduct SDMIII of P124 (Laccase) and P125 (EreB) + ligation product of F29+F30 + ligation product of F17+F19 + ligation product of F17+NK + ligation product of F29+NK into E. coli XL1 blue.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 2 µl of DNA was added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

Sequencing of P133 and P134

Investigators: Louise, Johanna

Aim of the experiment: Sequencing of two more QCII products (EreB) Procedure: The DNA was prepared for sequencing according to the Eurofins SmartSeq Kit protocol (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer).

The different genes we sequenced received the following barcodes:

Label Name Barcode1 Barcode2
p133 Miniprep of transformation of QC product of P109 (EreB, QC with O18/O19) (QC - SDMII - of EreB to remove forbidden PstI) FR01002287 (fw) FR01002296 (rev)
p134 Miniprep of transformation of QC product of P109 (EreB, QC with O18/O19) (QC - SDMII - of EreB to remove forbidden PstI) FR01002295 (fw) FR01002294 (rev)

Miniprep of overnight cultures of transformated E. coli XL1 blue of P114 and P115

Investigator: Andi

Aim of the experiment: Miniprep of overnight cultures of transformated E. coli XL1 blue of P114 and P115.

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)

Picking of of E. coli XL1 blue transformed with P45, P51, P100, P102

Investigator: Jeff, Leonie, Rosario

Aim of the experiment: Picking of of E. coli XL1 blue transformed with P45, P51, P100, P102.

Procedure:

  • Picked pipette tips was transferred into cell-culture tubes with air-permeable, sterile cover. Each tube contain 4 mL of LB-medium + 4 µL chloramphenicol(1000x) (P51, P100, P102)/4 µL Ampicillin (1000x) (P45).
  • 1 colony for each plasmid were picked.
  • These tubes were transferred in a cell culture shaker at 37 °C and were incubated overnight.

PCR of npt-Kasette (P144), PIF3 (P51), pActin (P143) and t35S (P143)

Investigator: Rosario, Leonie, Jeff

Aim of the experiment: PCR of npt-Kasette (P144), PIF3 (P51), pActin (P143) and t35S (P143).

Procedure:

Operational sequence:

  • PCR reaction mixture
volume reagent
10 µl 5x OneTaq Reaction Standard Reaction Buffer
1 µl 10 mM dNTPs
1 µl 10 µM Forward Primer (P143:O62 (pActin_for); P143:O60 (t35S_for); P144:O58 (npt-Kasette_for); P51:O66 (PIF3_for))
1 µl 10 µM Reverse Primer (P143:O63 (pActin_rev); P143:O61 (t35S_rev); P144:O59 (npt-Kasette_rev); P51:O67 (PIF3_rev))
0.25 µL OneTaq Hot Start DNA Polymerase (Finally: 1.25 units/50 µL)
1 µl Plasmid DNA (P114; P115; P51)
35.75 µL ddH2O Water
=50 µL TOTAL
  • Mix with pipette
  • The PCR program was performed after following scheme:
Initial denaturation 94 °C 30 s
30 cycles 94 °C 30 s
47 °C 60 s
68 °C 120 s
Final extension 68 °C 5 min
Hold 4 °C infinite
  • After PCR, the product was purified with QIAquick PCR Purification Kit, Qiagen.

Analytical gelelectrophoresis of F33, F34, F35, F36

Investigator: Jeff, Rosario, Leonie

Aim of the experiment: Analytical gelelectrophoresis of F33, F34, F35, F36.

Procedure:

  • 4 µl of F33, F34, F35 and F36 were mixed with seperately with 0.44 µl of DNA loading buffer (10x) and analytical gelelectrophoresis was performed at 1% agarose gel for 40 min at 90 V.

TUM13 20130528 PCR F33 F34 F35 F36.png

1 kbp ladder F33 F33 F33 F33
PCR did not work, maybe high GC content? PCR products has expected length, some byproducts PCR products has expected length, some byproducts PCR products has expected length

Wednesday, May 29th

Transformation of E. coli XL1 blue with SDMIII product of P124, ligation product of F29+F30 and ligation product of F17+F18

Investigator: Andi

Aim of the experiment: Transformation of E. coli XL1 blue with SDMIII product of P124, ligation product of F29+F30 and ligation product of F17+F18.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 5 µl of DNA was added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

Miniprep of overnight cultures of transformated E. coli XL1 blue of P100, P102, P51, P45

Investigator: Rosario

Aim of the experiment: Miniprep of overnight cultures of transformated E. coli XL1 blue of P100, P102, P51, P45 .

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)

Picking of of E. coli XL1 blue transformed with ligation product of F17+F28

Investigator: Andi

Aim of the experiment: Picking of of E. coli XL1 blue transformed with ligation product of F17+F28.

Procedure:

  • Picked pipette tips was transferred into cell-culture tubes with air-permeable, sterile cover. Each tube contain 4 mL of LB-medium + 4 µL chloramphenicol(1000x) (
  • 3 colonies were picked.
  • These tubes were transferred in a cell culture shaker at 37 °C and were incubated overnight.

Quick Change mutagenesis to remove forbidden restriction sites - SDMIII - of P133 (EreB)

Investigator: Louise

Aim of the experiment: Removal of forbidden restiction site from P133 (EreB).

Procedure: Quickchange - PCR

Reaction batch

volume reagent Additional information
2.5 µl 10x Pfu Ultra II buffer
1 µl Plasmid template (P133 - 1:10 dilution) need to get to 50 ng/µl
1 µl 1:10 dilution of O20 (for P133, 10 µM)
1 µl 1:10 dilution of O21 (for P133, 10 µM)
18 µl ddH2O
1 µl dNTP mix 50mM
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)


PCR cycling parameters - P133

Segment Cycles Temperature Time
1 1 95 °C 30 s
2 19 95 °C 30 s
52 °C 1 min
68 °C 3 min 30 s
  • Digestion of the parental DNA with DpnI: Addition of 1 µl DpnI to the reaction batch and incubate for 1 h at 37 °C.

Transformation of the Quickchange product into E. coli XL1 blue

Investigator: Louise

Aim of the experiment: Transformation of E. coli XL1 blue with Quickchangeproduct SDM III of P133.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 10 µl of DNA was added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

Preparative digestion of t35s(F34) with XbaI & PstI, npt(F25) with EcoRI & SpeI, PIF3(F36) with XbaI & AgeI-HF and P10 with XbaI & PstI as well as with EcoRI & SpeI

Investigator: Louise

Aim of the experiment: Preparative digestion of t35s(F34) with XbaI & PstI, npt(F25) with EcoRI & SpeI, PIF3(F36) with XbaI & AgeI-HF and P10 with XbaI & PstI as well as with EcoRI & SpeI.

Procedure:

  • Batch for preparative digestion of t35s(F34) with XbaI and PstI
volume reagent
25 µl Plasmid DNA P61
5 µl CutSmart Buffer
1 µl XbaI (20 U/µl)
1 µl PstI (20 U/µl)
18 µl ddH2O
=50 µl TOTAL
  • Batch for preparative digestion of npt(F35) with EcoRI and SpeI
volume reagent
25 µl Plasmid DNA P61
5 µl CutSmart Buffer
1 µl EcoRI (20 U/µl)
1 µl SpeI (20 U/µl)
18 µl ddH2O
=50 µl TOTAL
  • Batch for preparative digestion of PIF3(F36) with XbaI and AgeI-HF
volume reagent
25 µl Plasmid DNA P61
5 µl CutSmart Buffer
1 µl XbaI (20 U/µl)
1 µl AgeI-HF (20 U/µl)
18 µl ddH2O
=50 µl TOTAL
  • Batch for preparative digestion of P10 with XbaI & PstI for backbone isolation.
volume reagent
20 µl Plasmid DNA P96
4 µl CutSmart Buffer
1 µl XbaI (20 U/µl)
1 µl PstI (20 U/µl)
14 µl ddH2O
=40 µl TOTAL
  • Batch for preparative digestion of P10 with EcoRI and SpeI for backbone isolation.
volume reagent
20 µl Plasmid DNA P96
4 µl CutSmart Buffer
1 µl EcoRI (20 U/µl)
1 µl SpeI (20 U/µl)
14 µl ddH2O
=40 µl TOTAL
  • Incubation for 2.5 h at 37 °C.
  • The resulting fragments were named: ?????
  • 5 µl of DNA loading buffer (10x) were added to the 50 µl reaction batches and 4 µl of DNA loading buffer (10x) were added to the 40 µl reaction batches after digestion and were loaded on a 1% agarose gel for preparative gelelectrophoresis.
  • Preparative gelelectrophoresis was performed at 90 V for 90 min.

TUM13 20130529 prep Verd F34 Xba.PstI F35 EcoRI.SpeI F36 XbaI.AgeI.png

1 kbp ladder DNA ladder Digestion of PCR product t35s (F34) with XbaI & PstI = F38 Digestion of PCR product npt casette (F25) with EcoRI & SpeI = F39 Digestion of PCR product PIF3 (F36) with XbaI & AgeI-HF = F40
as expected, lower band was cut out as expected, bright band was cut out as expected, bright band was cut out


TUM13 20130529 prep Verdau P10 EcoRI.SpeI P10 XbaI.PstI.png

1 kbp ladder DNA ladder Digestion of P10 with EcoRI & SpeI = F41 Digestion of P10 with XbaI & PstI = F42
as expected, lower band was cut out as expected, lower band was cut out
  • Bands were extracted by QIAquick Gel Extraction Kit, QIAGEN.

Transformation of E. coli XL1 blue with pSB1C3 containing a NLS from SV40 (BBa_K801030)

Investigator: Florian, Jeff

Aim of the experiment: Transformation of E. coli XL1 blue with pSB1C3 containing a NLS from SV40 (BBa_K801030).

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 10 µl of DNA was added to 200 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

PCR of pActin (P143)

Investigator: Florian, Jeff

Aim of the experiment: PCR of pActin (P143).

Procedure:

Operational sequence:

  • PCR reaction mixture
volume reagent
10 µl 5x OneTaq Reaction Buffer
1 µl 10 mM dNTPs
1 µl 10 µM Forward Primer (P143:O62 (pActin_for))
1 µl 10 µM Reverse Primer (P143:O63 (pActin_rev))
0.25 µL OneTaq Hot Start DNA Polymerase (Finally: 1.25 units/50 µL)
1 µl Plasmid DNA (P143)
35.75 µL ddH2O Water
=50 µL TOTAL
  • Mix with pipette
  • The PCR program was performed after following scheme:
Initial denaturation 94 °C 30 s
30 cycles 94 °C 30 s
51 °C 60 s
68 °C 80 s
Final extension 68 °C 5 min
Hold 4 °C infinite
  • After PCR, the product was purified with QIAquick PCR Purification Kit, Qiagen.

Results:

  • After analytical gelelectrophoresis there was no product visible. PCR did't work!

Ligation of F17+F40 (PIF3 in pSB1C3(RFC25)), F42+F38 (t35S in pSB1C3(RFC10)) and F41+F39(npt-casette in pSB1C3(RFC10))

Investigator: Jeff

Aim of the experiment: Ligation of F17+F40 (PIF3 in pSB1C3(RFC25)), F42+F38 (t35S in pSB1C3(RFC10)) and F41+F39(npt-casette in pSB1C3(RFC10)).

Procedure:

  • Ligation batch for F17+F40:
volume reagent
1.63 µl F17 (61.4 ng/µl, 2086 bp)
1.88 µl F40 (22.8 ng/µl, ~297 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
13.49 µl ddH2O
=20 µl TOTAL
  • Ligation batch for F42+F38:
volume reagent
1.36 µl F42 (73.5 ng/µl, 2070 bp)
3.42 µl F38 (9.2 ng/µl, 217 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
12.22 µl ddH2O
=20 µl TOTAL
  • Ligation batch for F41+F39:
volume reagent
1.11 µl F41 (89.9 ng/µl, 2070 bp)
13.74 µl F39 (16.0 ng/µl, 1517 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
2.15 µl ddH2O
=20 µl TOTAL
  • Negative control was also prepared. Instead of the insert, the same volume of ddH2O was added to the reaction batch.
  • Cycled ligation has been performed after following protocol in a thermocycler:
99 cycles 12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
Hold 16 °C infinite
  • Lid temperature = 37 °C

Thursday, May 30th

Gradient PCR of pActin (P143)

Investigator: Ingmar

Aim of the experiment: PCR of pActin

Procedure:

Operational sequence:

  • PCR reaction mixture
volume reagent
10 µl 5x OneTaq Reaction Standard Reaction Buffer
1 µl 10 mM dNTPs
1 µl 10 µM Forward Primer O62 (pActin_for)
1 µl 10 µM Reverse Primer O63 (pActin_rev)
0.25 µL OneTaq Hot Start DNA Polymerase (Finally: 1.25 units/50 µL)
1 µl Plasmid DNA P143
35.75 µL ddH2O Water
=50 µL TOTAL
  • PCR reaction mixture
volume reagent
10 µl 5x OneTaq GC Reaction Buffer
1 µl 10 mM dNTPs
1 µl 10 µM Forward Primer O62 (pActin_for)
1 µl 10 µM Reverse Primer O63 (pActin_rev)
0.25 µL OneTaq Hot Start DNA Polymerase (Finally: 1.25 units/50 µL)
1 µl Plasmid DNA P143
35.75 µL ddH2O Water
=50 µL TOTAL
  • Mix with pipette
  • The PCR program was performed after following scheme:
Initial denaturation 94 °C 30 s
30 cycles 94 °C 30 s
47 °C 60 s
68 °C 120 s
Final extension 68 °C 5 min
Hold 4 °C infinite

A temperature gradient was applied beginning at 47°C and ranging to 51°C. For each integer (47, 48, 49, 50 and 51°C) a single PCR batch was used.

  • After PCR, the product was purified with QIAquick PCR Purification Kit, Qiagen.


Analytical gelelectrophoresis Procedure:

  • 4 µl of each PCR product were mixed seperately with 0.44 µl of DNA loading buffer (10x) and analytical gelelectrophoresis was performed at 1% agarose gel for 60 min at 90 V.

TUM13 20130530 grad PCR P143 O62.O63 GCbuffer standardbuffer.png

1 kbp ladder F45 GC buffer F46 GC buffer F47 GC buffer F47 GC buffer F49 GC buffer normal buffer normal buffer normal buffer normal buffer normal buffer 1 kbp ladder
PCR products has expected length PCR products has expected length PCR products has expected length PCR products has expected length PCR products has expected length PCR products has expected length, some byproducts PCR products has expected length, some byproducts PCR products has expected length, some byproducts PCR products has expected length, some byproducts PCR products has expected length, some byproducts

Miniprep of overnight cultures of transformated E. coli XL1 blue of F17+F28 (FluA in pSB1C3 RFC25)

Investigator: Jeff, Flo

Aim of the experiment: Miniprep of overnight cultures of transformated E. coli XL1 blue of F17+F28 (FluA in pSB1C3 RFC25).

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)

Analytical digestion and gelelectrophoresis of ligation products F17+F28 (FluA in pSB1C3 RFC25)

Investigator: Flo, Jeff

Aim of the experiment: Analytical digestion and gelelectrophoresis of ligation products F17+F28 (FluA in pSB1C3 RFC25).

Procedure:

  • Analytical digestion of ligation products of F17+F28 (FluA in pSB1C3 RFC25) with XbaI & AgeI.
volume reagent
2.5 µl P150/P151/P152/P153
2 µl CutSmart Buffer (10x)
0.25 µl XbaI
0.25 µl AgeI-HF
15 µl ddH2O
=20 µl TOTAL
  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed at 90 V for 60 min.

TUM13 20130530 anal Verd P150-P153 XbaI.AgeI.png

1 kbp ladder DNA ladder# Digestion of P150 with XbaI&AgeI-HF Digestion of P151 with XbaI&AgeI-HF Digestion of P152 with XbaI&AgeI-HF Digestion of P153 with XbaI&AgeI-HF
as expected as expected as expected as expected

Preparative gelelectrophoresis of oligohybridization products F31 & F32

Investigator: Flo, Jeff

Aim of the experiment: Preparative gelelectrophoresis of oligohybridization products F31 & F32.

Procedure:

  • 50 µl of the 1:10 dilution of F31 and F32 were mixed with 5 µl of DNA loading buffer (10x).
  • Preparative gelelectrophoresis was performed 1.5 h on a 2% agarose gel at 90 V.

TUM13 20130530 F31 F32.png

1 kbp ladder F31 F32
  • Bands were extracted by QIAquick Gel Extraction Kit, QIAGEN.
  • Gelpurified F31 and F32 were labelled as F43 and F44.

Transformation of E. coli XL1 blue with F17+F40 (PIF3 in pSB1C3(RFC25)), F42+F38 (t35S in pSB1C3(RFC10)) and F41+F39(npt-casette in pSB1C3(RFC10))

Investigator: Florian, Jeff

Aim of the experiment: Transformation of E. coli XL1 blue with F17+F40 (PIF3 in pSB1C3(RFC25)), F42+F38 (t35S in pSB1C3(RFC10)) and F41+F39(npt-casette in pSB1C3(RFC10)).

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 10 µl of DNA were added to 200 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellets were resuspended in 100 µl of LB-medium and these concentrated cell suspensions were plated again on a new chlorampenicol plates.

Ligation of F42+F43 and F17+F32

Investigator: Rosario

Aim of the experiment: Ligation of F42+F43 and F17+F32.

Procedure:

  • Ligation batch for F42+F43:
volume reagent
1.36 µl F42 (73.5 ng/µl, 2070 bp)
1.51 µl F43 (5.4 ng/µl, 34 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
14.13 µl ddH2O
=20 µl TOTAL
  • Ligation batch for F17+F32:
volume reagent
1.63 µl F17 (61.4 ng/µl, 2086 bp)
0.25 µl F32 (2510.8 ng/µl, 49 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
15.12 µl ddH2O
=20 µl TOTAL
  • Negative control was also prepared. Instead of the insert, the same volume of ddH2O was added to the reaction batch.
  • Cycled ligation has been performed after following protocol in a thermocycler:
99 cycles 12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
Hold 16 °C infinite
  • Lid temperature&

Picking of of E. coli XL1 blue transformed with EreB SDMIII (P149) and BBa_K801030 (SV40 NLS)

Investigator: Louise

Aim of the experiment: Picking of of E. coli XL1 blue transformed with EreB SDMIII (P149) and BBa_K801030 (SV40 NLS).

Procedure:

  • Picked pipette tips was transferred into cell-culture tubes with air-permeable, sterile cover. Each tube contain 4 mL of LB-medium + 4 µL chloramphenicol(1000x).
  • 5 colonies of EreB SDMIII (P149) and 2 colonies of BBa_K801030 (SV40 NLS) were picked.
  • These tubes were transferred in a cell culture shaker at 37 °C and were incubated overnight.

Friday, May 31st

Miniprep of overnight cultures of transformated E. coli XL1 blue with P149 (QCIII of EreB) and BBa_K801030 (SV40 NLS)

Investigator: Louise, Jeff, Leonie, Katrin

Aim of the experiment: Miniprep of overnight cultures of transformated E. coli XL1 blue with P149 (QCIII of EreB) and BBa_K801030 (SV40 NLS)

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)

Analytical digestion and gelelectrophoresis of P149 (QCIII of EreB) with EcoRI-HF and PstI-HF

Investigator: Louise, Jeff, Leonie, Katrin

Aim of the experiment: Analytical digestion and gelelectrophoresis of P154-P158 (QCIII of EreB) with EcoRI-HF and PstI-HF to check if QCII was successful

Procedure:

  • Analytical digestion of P154-P158 (QCIII of EreB) with EcoRI-HF and PstI-HF
volume reagent
2.5 µl P149-P158/P133 (control before QCIII)
2 µl CutSmart Buffer (10x)
0.25 µl EcoRI-HF
0.25 µl PstI-HF
15 µl ddH2O
=20 µl TOTAL
  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed at 90 V for 60 min.

TUM13 20130531 anal Verd QCIII P133 P154-158 EcoRI,PstII.png

1 kbp ladder DNA ladder# Digestion of P133 with EcoRI-HF and PstI-HF Digestion of P154 with EcoRI-HF and PstI-HF Digestion of P155 with EcoRI-HF and PstI-HF Digestion of P156 with EcoRI-HF and PstI-HF Digestion of P157 with EcoRI-HF and PstI-HF Digestion of P158 with EcoRI-HF and PstI-HF
as expected as expected as expected as expected as expected as expected

Sequencing of P157 and P160

Investigators: Louise, Jeff, Leonie, Katrin

Aim of the experiment: Sequencing of QCIII product (EreB) and BBa_K801030 (SV40 NLS)

Procedure: The DNA was prepared for sequencing according to the Eurofins SmartSeq Kit protocol (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer).

The different genes we sequenced received the following barcodes:

Label Name Barcode1 Barcode2
P157 Miniprep of transformation of QCIII product of P149 (QC - SDMIII - of EreB to remove forbidden PstI) FR01002291 (VR) FR01002292 (VF2)
P160 Miniprep of transformation of BBa_K801030 (SV40 NLS) FR01002289 (VR) FR01002290 (VF2)

Ligation of F29+F30

Investigator: Leonie, Katrin

Aim of the experiment: Ligation of F29+F30

Procedure:

  • Ligation batch
volume reagent
4.22 µl F29 (23.7 ng/µl, 2110 bp))
10.48 µl F30 (9,5 ng/µl, about 700 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
2.3 µl ddH2O
=20 µl TOTAL


No negative control was prepared because there was not enough vector backbone left Ligation was performed at 37 °C overnight

Quick Change mutagenesis to remove forbidden restriction sites - SDMIII - of P124 (Laccase)

Investigator: Louise, Leonie, Katrin

Aim of the experiment: Removal of forbidden restiction site from P124 (Laccase).

Procedure: Quickchange - PCR

Reaction batch

volume reagent Additional information
2.5 µl 10x Pfu Ultra II buffer
1 µl Plasmid template (P124 - 1:10 dilution) need to get between 5 and 50 ng/µl
1 µl 1:10 dilution of O30 (for P124, 10 µM)
1 µl 1:10 dilution of O31 (for P124, 10 µM)
18 µl ddH2O
1 µl dNTP mix 50mM
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)


PCR cycling parameters - P124

Segment Cycles Temperature Time
1 1 95 °C 30 s
2 19 95 °C 30 s
52 °C 1 min
68 °C 4 min
4 °C hold

After the PCR; 1 µl of Dpn1 was added and the reaction mixture was incubated at 37°C for one hour

Preparative digestion of pActin(F46) with XbaI & PstI

Investigator: Ingmar

Aim of the experiment: Preparative digestion of pActin(F46) in order to ligat this fragment in pSB1C3 later on.

Procedure:

  • Batch for preparative digestion of pActint(F46) with XbaI and PstI
volume reagent
25 µl F46 PCR product of pActin
5 µl CutSmart Buffer
1 µl XbaI (20 U/µl)
1 µl PstI (20 U/µl)
18 µl ddH2O
=50 µl TOTAL
  • Incubation for 3 h at 37 °C.
  • 5 µl of DNA loading buffer (10x) were added to the 50 µl reaction batchesand loaded on a 1% agarose gel for preparative gelelectrophoresis.
  • Preparative gelelectrophoresis was performed at 90 V for 90 min.

TUM13 20130531 prep Verd F46 pActin XbaI+PstI.Tif

  • The band was extracted by QIAquick Gel Extraction Kit, QIAGEN. The resulting fragment was named: F50

Ligation of F42+F50 (pActin in pSB1C3)

Investigator: Ingmar

Aim of the experiment: Ligation of F42+F50 (pActin in pSB1C3(RFC25).

Procedure:

  • Ligation batch
volume reagent
1.37 µl F42
13.13 µl F50
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
2.5 µl ddH2O
=20 µl TOTAL
  • Negative control was also prepared. Instead of the insert, the same volume of ddH2O was added to the reaction batch.
  • Cycled ligation has been performed after following protocol in a thermocycler:
99 cycles 12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
Hold 16 °C infinite
  • Lid temperature = 37 °C

Picking of of E. coli XL1 blue transformed with F42+F38 (t35S), F17+F40 (Pif 3) and F41+F39 (npt)

Investigator: Ingmar

Aim of the experiment: Picking of of E. coli XL1 blue transformed with F42+F38 (t35S), F17+F40 (Pif 3) and F41+F39 (npt).

Procedure:

  • The picked colonies were transferred into cell-culture tubes with air-permeable, sterile cover containing 5 mL of LB-medium + 5 µL chloramphenicol(1000x).
  • 3 colonies of each agar plate were picked.
  • These tubes were transferred in a cell culture shaker at 37 °C and were incubated overnight.

Transformation of E. coli XL1 blue with ligation products F42+F43 and F17+F32

Investigator: Louise, Jeff

Aim of the experiment: Transformation of E. coli XL1 blue with ligation products F42+F43 and F17+F32.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 10 µl of DNA was added to 200 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellets were resuspended in 100 µl of LB-medium and these concentrated cell suspensions were plated again on new chlorampenicol plates.

Saturday, June 1st

Transformation of E. coli XL1 blue with ligation products F29+F30 (GFP in pSB1C3), F42+F50 (actin promoter in pSB1C3), F42+F50 (negative control)

Investigator: Leonie, Katrin

Aim of the experiment: Transformation of E. coli XL1 blue with ligation products F29+F30 (GFP in pSB1C3), F42+F50 (actin promoter in pSB1C3), F42+F50 (negative control)

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 5 µl of DNA were added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellets were resuspended in 100 µl of LB-medium and these concentrated cell suspensions were plated again on a new chlorampenicol plates.

Transformation of E. coli XL1 blue with QCIII product of Laccase (SDMIII of P124)

Investigator: Leonie, Katrin

Aim of the experiment: Transformation of E. coli XL1 blue with QCIII product of Laccase

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 10 µl of DNA were added to 100 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellets were resuspended in 100 µl of LB-medium and these concentrated cell suspensions were plated again on a new chlorampenicol plates.

Miniprep of overnight cultures of transformated E. coli XL1 blue with F39 + F41 (npt-casette in pSC1C3),F42+F38 (t35s in pSB1C3), F17+F40 (PIF3 in pSB1C3)

Investigator: Leonie, Katrin

Aim of the experiment: Miniprep of overnight cultures of transformated E. coli XL1 blue with F39 + F41 (npt-casette in pSC1C3),F42+F38 (t35s in pSB1C3), F17+F40 (PIF3 in pSB1C3)

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)

Analytical digestion and gelelectrophoresis of P161-163 (F39 + F41, npt-casette in pSB1C3), P164-166 (F42+F38, t35s in pSB1C3), P167-169 (F17+F40, PIF3 in pSB1C3)

Investigator: Leonie, Katrin

Aim of the experiment: Analytical digestion and gelelectrophoresis of P161-163 (F39 + F41, npt-casette in pSC1C3) with EcoRI-HF and SpeI-HF, P164-166 (F42+F38, t35s in pSB1C3) with EcoRI-HF and SpeI-HF and P167-169 (F17+F40, PIF3 in pSB1C3) with AgeI-HF and XbaI

Procedure:

  • Analytical digestion of P161-163 (F39 + F41, npt-casette in pSC1C3), P164-166 (F42+F38, t35s in pSB1C3) with EcoRI-HF and SpeI-HF
volume reagent
2.5 µl P161-P166
2 µl CutSmart Buffer (10x)
0.25 µl EcoRI-HF
0.25 µl SpeI-HF
15 µl ddH2O
=20 µl TOTAL
  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed at 90 V for 60 min.


  • Analytical digestion of P167-169 (F17+F40, PIF3 in pSB1C3) with AgeI-HF and XbaI
volume reagent
2.5 µl P167-P169
2 µl CutSmart Buffer (10x)
0.25 µl AgeI-HF
0.25 µl XbaI
15 µl ddH2O
=20 µl TOTAL
  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed at 90 V for 60 min.

TUM 13 20130601 anal Verd F41+39 EcoRI SpeI F42+38 EcoRI SpeI F17+40 XbaI+AgeI.png

1 kbp ladder DNA ladder# Digestion of P161 with EcoRI-HF and SpeI-HF Digestion of P162 with EcoRI-HF and SpeI-HF Digestion of P163 with EcoRI-HF and SpeI-HF Digestion of P164 with EcoRI-HF and SpeI-HF Digestion of P165 with EcoRI-HF and SpeI-HF Digestion of P166 with EcoRI-HF and SpeI-HF Digestion of P167 with AgeI-HF and XbaI Digestion of P168 with AgeI-HF and XbaI Digestion of P169 with AgeI-HF and XbaI
as expected as expected as expected as expected as expected as expected as expected as expected as expected

Sunday, June 2nd

Picking of of E. coli XL1 blue transformed with QCIII product of P124 and the ligation products of F17+F44 and F42+F32

Investigator: Andi

Aim of the experiment: Picking of of E. coli XL1 blue transformed with QCIII product of P124 and the ligation products of F17+F32 and F42+F32.

Procedure:

  • The picked colonies were transferred into cell-culture tubes with air-permeable, sterile cover containing 4 mL of LB-medium + 4 µL chloramphenicol(1000x).
  • 4 colonies of each agar plate were picked.
  • These tubes were transferred in a cell culture shaker at 37 °C and were incubated overnight.

Week 7

Monday, June 3rd

Analytical digestion and gelelectrophoresis of P170-P173 (F17+F32, SpyTag in pSB1C3 RFC25), P174-P177 (F42+F43, miniMCSII in pSB1C3 RFC10), P178-181 (QCIII von P142, Laccase in pSB1C3 RFC10)

Investigator: Andi, Johanna, Leonie, Jeff

Aim of the experiment: Analytical digestion and gelelectrophoresis of P170-P173 (F17+F32, SpyTag in pSB1C3 RFC25), P174-P177 (F42+F43, miniMCSII in pSB1C3 RFC10), P178-181 (QCIII von P142, Laccase in pSB1C3 RFC10).

Procedure:

  • Mastermix for analytical digestion of P170-P173 (F17+F32, SpyTag in pSB1C3 RFC25), P174-P177 (F42+F43, miniMCSII in pSB1C3 RFC10) with XbaI+PstI.
volume reagent
18 µl CutSmart Buffer (10x)
2.25 µl EcoRI-HF
2.25 µl SpeI-HF
135 µl ddH2O
=157.5 µl TOTAL
  • 17.5 µl of the mastermix was added to 2.5 µl of plasmid DNA (P170-P177)
  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed at 90 V for 60 min.


  • Analytical digestion of P178-181 (QCIII von P142, Laccase in pSB1C3 RFC10):
volume reagent
2.5 µl P178-P181
2 µl CutSmart Buffer (10x)
0.25 µl NgoMIV
0.25 µl PstI-HF
15 µl ddH2O
=20 µl TOTAL
  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed at 90 V for 60 min.

TUM13 20130603 anal Verd P170-P177 EcoRI.PstI.png

1 kbp ladder DNA ladder Digestion of P170 with EcoRI-HF and PstI-HF Digestion of P162 with EcoRI-HF and PstI-HF Digestion of P163 with EcoRI-HF and PstI-HF Digestion of P164 with EcoRI-HF and PstI-HF Digestion of P164 with EcoRI-HF and PstI-HF Digestion of P164 with EcoRI-HF and PstI-HF Digestion of P164 with EcoRI-HF and PstI-HF Digestion of P164 with EcoRI-HF and PstI-HF Digestion of P164 with EcoRI-HF and PstI-HF
as expected, insert too small to be visible as expected, insert too small to be visible as expected, insert too small to be visible as expected, insert too small to be visible as expected, insert too small to be visible as expected, insert too small to be visible as expected, insert too small to be visible as expected, insert too small to be visible as expected, insert too small to be visible


TUM13 20130603 anal Verd P142 NgoMIV.PstI P178-P181 NgoMIV.PstI.png

1 kbp ladder DNA ladder Digestion of P142 with NgoMIV and PstI-HF Digestion of P178 with NgoMIV and PstI-HF Digestion of P179 with NgoMIV and PstI-HF Digestion of P180 with NgoMIV and PstI-HF Digestion of P181 with NgoMIV and PstI-HF
Ctrl (before QuickChange III) as expected, plasmid is only linearized, all NgoMIV sites are removed as expected, plasmid is only linearized, all NgoMIV sites are removed as expected, plasmid is only linearized, all NgoMIV sites are removed as expected, plasmid is only linearized, all NgoMIV sites are removed

Tuesday, June 4th

Sequencing of P162(npt-cassete), P165(t35s), P168(PIF3), P179(LaccQCIII), P177(MiniMCS), P170(Spytag)

Investigators: Louise, Johanna

Aim of the experiment: Sequencing of P162(npt-cassete), P165(t35s), P168(PIF3), P179(LaccQCIII), P177(MiniMCS), P170(Spytag).

Procedure: The DNA was prepared for sequencing according to the Eurofins SmartSeq Kit protocol (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer).

The different genes we sequenced received the following barcodes:

Label Name Barcode1 Barcode2
P162 Miniprep of ligation product F39 + F41 (npt-casette in pSB1C3) FR01002331 (VR) FR01002330 (VF2)
P165 Miniprep of ligation product F42+F38 (t35s in pSB1C3) FR01002332 (VF2)
P168 Miniprep of ligation product F17+F40 (PIF3 in pSB1C3) FR01002333 (VF2)
P179 Miniprep of ligation product Laccase QCIII (P142) FR01002335 (VR) FR01002334 (VF2)
P177 Miniprep of ligation product MiniMCSII F42+F43 FR01002336 (VF2)
P170 Miniprep of ligation product F17+F32 (SpyTag) FR01002328 (VF2)

Preparative digestion and gelelectrophoresis of P39(middle-linker) with PstI and AgeI-HF, P20(GFP-Psb1C3) with NgoMIV and PstI, F45(pActin) with XbaI and PstI

Investigator: Louise, Johanna

Aim of the experiment: Preparative digestion of P39(middle-linker) with PstI and AgeI-HF, P20(GFP-Psb1C3) with NgoMIV and PstI, F45(pActin) with XbaI and PstI.

Procedure:

  • Batch for preparative digestion of P39(middle-linker) with PstI and AgeI-HF
volume reagent
15 µl Plasmid DNA P39
4 µl CutSmart Buffer
1 µl AgeI-HF(20 U/µl)
1 µl PstI (20 U/µl)
19 µl ddH2O
=40 µl TOTAL
  • Batch for preparative digestion of P20(GFP-Psb1C3) with NgoMIV and PstI
volume reagent
20 µl Plasmid DNA P20
4 µl CutSmart Buffer
1 µl NgoMIV (20 U/µl)
1 µl PstI (20 U/µl)
14 µl ddH2O
=40 µl TOTAL
  • Batch for preparative digestion of F45(pActin) with XbaI and PstI
volume reagent
25 µl Fragment DNA F45
5 µl CutSmart Buffer
1 µl XbaI (20 U/µl)
1 µl PstI (20 U/µl)
18 µl ddH2O
=50 µl TOTAL
  • Incubation for 3 h at 37 °C.
  • 5 µl of DNA loading buffer (10x) were added to the 50 µl reaction batches and 4 µl of DNA loading buffer (10x) were added to the 40 µl reaction batches after digestion and were loaded on a 1% agarose gel for preparative gelelectrophoresis.
  • Preparative gelelectrophoresis was performed at 90 V for 90 min.

TUM13 20130604 prep Verd P20 NgoMIV.PstI P39 AgeI.Pst F45 XbaI.PstI.png

1 kbp DNA ladder Digestion of P20 with NgoMIV & PstI = F53 Digestion of P39 with AgeI & PstI = F52 Digestion of F45 with XbaI & PstI = F51
as expected, lower band was cut out as expected, band was cut out as expected, lower band was cut out
  • Bands were extracted by QIAquick Gel Extraction Kit, QIAGEN.

Quick Change mutagenesis to remove forbidden restriction sites - SDMIV - of P179 (Laccase)

Investigator: Andi, Jeff

Aim of the experiment: Removal of forbidden restiction site SDM IV from P179 (Laccase).

Procedure: Quickchange - PCR

Reaction batch

volume reagent Additional information
2.5 µl 10x Pfu Ultra II buffer
1 µl Plasmid template (P179 - 1:6 dilution) need to get between 5 and 50 ng/µl
1 µl 1:10 dilution of O32 (for P179, 10 µM)
1 µl 1:10 dilution of O33 (for P179, 10 µM)
18 µl ddH2O
1 µl dNTP mix 50mM
0.5 µl Pfu Ultra II DNA polymerase (2.5 U / µl)


PCR cycling parameters - P179

Segment Cycles Temperature Time
1 1 95 °C 30 s
2 19 95 °C 30 s
52 °C 1 min
68 °C 4 min
4 °C hold

After the PCR; 1 µl of Dpn1 was added and the reaction mixture was incubated at 37°C for one hour

Preparative digestion and gelelectrophoresis of P182 (Gensynthesis 1) with XbaI and AgeI-HF, P183 (Gensynthesis 2) with XbaI and AgeI-HF

Investigator: Andi, Jeff

Aim of the experiment: Preparative digestion and gelelectrophoresis of P182 (Gensynthese 1) with XbaI and AgeI-HF, P183 (Gensynthese 2) with XbaI and AgeI-HF

Procedure:

  • Batch for preparative digestion of P182 with XbaI and AgeI-HF
volume reagent
15 µl Plasmid DNA P182
4 µl CutSmart Buffer
1 µl AgeI-HF(20 U/µl)
1 µl XbaI (20 U/µl)
19 µl ddH2O
=40 µl TOTAL
  • Batch for preparative digestion of P183 with XbaI and AgeI- HF
volume reagent
15 µl Plasmid DNA P183
4 µl CutSmart Buffer
1 µl AgeI-HF (20 U/µl)
1 µl XbaI (20 U/µl)
19 µl ddH2O
=40 µl TOTAL
  • Incubation for 2.5 h at 37 °C.
  • 4 µl of DNA loading buffer (10x) were added to the 40 µl reaction batches after digestion and were loaded on a 1.5% agarose gel for preparative gelelectrophoresis.
  • Preparative gelelectrophoresis was performed at 70 V for 60 min.

TUM13 20130604 prep verdau P182-183 XbaI,AgeI.png

1 kbp DNA ladder Digestion of Gensynthesis 1 with XbaI & AgeI 100 bp DNA ladder Digestion of Gensynthesis 2 with XbaI & AgeI 1 kbp DNA ladder
as expected, fragments (78 bp and 530 bp) were cut out as expected, fragments (111 bp, 206 bp and 359 bp) were cut out
  • Bands were extracted by QIAquick Gel Extraction Kit, QIAGEN.

Preparative digestion and gelelectrophoresis of P9 with XbaI and AgeI-HF

Investigator: Andi, Jeff, Leonie

Aim of the experiment: Preparative digestion and gelelectrophoresis of P9 with XbaI and AgeI-HF

Procedure:

  • Batch for preparative digestion of P9 with XbaI and AgeI-HF
volume reagent
15 µl Plasmid DNA P9
4 µl CutSmart Buffer
1 µl AgeI-HF(20 U/µl)
1 µl XbaI (20 U/µl)
19 µl ddH2O
=40 µl TOTAL
  • Incubation for 2.5 h at 37 °C.
  • The resulting fragments were named: ?????
  • 4 µl of DNA loading buffer (10x) were added to the 40 µl reaction batches after digestion and were loaded on a 1% agarose gel for preparative gelelectrophoresis.
  • Preparative gelelectrophoresis was performed at 70 V for 60 min.

TUM13 20130604 prep verdau P9 XbaI.AgeI.png

  • Gelfragmentation was like expected, both bands were cut out (upper band = PhyB, lower band = pSB1C3 RFC25)
  • Bands were extracted by QIAquick Gel Extraction Kit, QIAGEN.

Transformation of E. coli XL1 blue with Quickchange product SDM IV of P179 (Laccase)

Investigator: Andi, Jeff

Aim of the experiment: Transformation of E. coli XL1 blue with Quickchange product SDM IV of P179 (Laccase).

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 2x 10 µl of DNA was added seperately into 2x 200 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellets were resuspended in 100 µl of LB-medium and these concentrated cell suspensions were plated again on new chlorampenicol plates.

Transformation of E. coli XL1 blue with P39

Investigator: Louise, Johanna

Aim of the experiment: Transformation of E. coli XL1 blue with P39

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 10 µl of DNA was added seperately into 200 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of the cell suspension was plated on one chloramphenicol plate.
  • The rest were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellets were resuspended in 100 µl of LB-medium and these concentrated cell suspensions were plated again on new chlorampenicol plates.

Preparative digestion and gelelectrophoresis of P39 with AgeI & PstI, P20 with NgoMIV & PstI

Where is the snapshot of the gel =DDDD

Investigator: Johanna, Louise

Aim of the experiment:Preparative digestion of P39 with AgeI & PstI, P20 with NgoMIV & PstI to fusion Middle linker of P39 with GFP of P20.

Procedure:

Batch for preparative digestion of P39 (Middle-Linker) with PstI and AgeI.

volume reagent
20 µl P39
4 µl NEBuffer 4
0.4 µl BSA (100x)
2 µl AgeI-HF
2 µl PstI
11.6 µl ddH2O
=40 µl TOTAL

Batch for preparative digestion of P20 (GFP-Psb1C3) with NgoMIV and PstI.

volume reagent
20 µl P45
4 µl NEBuffer 4
0.4 µl BSA (100x)
2 µl NgoMIV
2 µl PstI
11.6 µl ddH2O
=40 µl TOTAL
  • Incubation for 150 min at 37 °C.
  • Preparative gelelectrophoresis was performed at 90 V for 1 h.

File:FOTOFOTO.png

1 kbp ladder P20 digested with NgoMIV&PstI (=F30) P39 digested with NgoMIV&PstI (=F30)
lower band was cut out band was cut out
  • Bands were extracted by QIAquick Gel Extraction Kit, QIAGEN.

Ligation of F58+F59, F55+F59, F54+F59, F56+F59, F57+F59, F52+F53, F42+F51

Investigator: Jeff, Andi, Johanna, Louise, Leonie

Aim of the experiment: Ligation of F53+F59, F58+F59, F55+F59, F54+F59, F56+F59, F57+F59, F52+F53, F42+F51.

Procedure:

  • Ligation batch for F54+F59 :
volume reagent
2.2 µl F54 (5.9 ng/µl, 90 bp)
1.5 µl F59 (66.7 ng/µl, 2100 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
13.3 µl ddH2O
=20 µl TOTAL
  • Ligation batch for F55+F59:
volume reagent
11.6 µl F55 (6.4 ng/µl, 520 bp)
1.5 µl F59 (66.7 ng/µl, 2100 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
3.9 µl ddH2O
=20 µl TOTAL
  • Ligation batch for F56+F59:
volume reagent
3.3 µl F56 (4.7 ng/µl, 110 bp)
1.5 µl F59 (66.7 ng/µl, 2100 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
12.2 µl ddH2O
=20 µl TOTAL
  • Ligation batch for F57+F59:
volume reagent
3.1 µl F57 (9.1 ng/µl, 200 bp)
1.5 µl F59 (66.7 ng/µl, 2100 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
12.4 µl ddH2O
=20 µl TOTAL
  • Ligation batch for F58+F59:
volume reagent
4.4 µl F58 (12.9 ng/µl, 400 bp)
1.5 µl F59 (66.7 ng/µl, 2100 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
11.1 µl ddH2O
=20 µl TOTAL
  • Negative Control Ligation batch for F59:
volume reagent
1.5 µl F59 (66.7 ng/µl, 2100 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
15.5 µl ddH2O
=20 µl TOTAL
  • Ligation batch for F52+F53:
volume reagent
10 µl F52 (9.9 ng/µl, XXX bp)
7 µl F53 (12.2 ng/µl, XXX bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
=20 µl TOTAL
  • Ligation batch for F42+F51:
volume reagent
1.36 µl F42 (XXX ng/µl, XXX bp)
15.64 µl F51 (8.2 ng/µl, 1237 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
=20 µl TOTAL
  • Negative control was also prepared. Instead of the insert, the same volume of ddH2O was added to the reaction batch.
  • Cycled ligation has been performed after following protocol in a thermocycler:
99 cycles 12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
12 °C 60 s
22 °C 60 s
Hold 16 °C infinite
  • Lid temperature = 37 °C

Plating of received E. coli containing biobricks

Investigator: Jeff, Andreas, Leonie

Aim of the experiment: The received biobricks were already transformed in E. coli and were in an agar stabs. These E. coli cells were transferred with an inoculation loop on antibiotic selection plates and were incubated over night.

Operational sequence:

  • Bacterias containing plasmids with biobricks were transferred with a sterile inoculation loop on antibiotic plates and were incubated at 37 °C overnight.
  • The biobricks were:
Name Function
BBa_J61032 Alkaline Phosphatase
BBa_K426020 Self lysis device
BBa_K729004 Nuclease from S. Aureus
BBa_K365001 PIF6
BBa_K648011 RBS B0034 with cI repressor C0051 under the control of constitutive promoter J23113

Wednesday, June 5th

Transformation of E. coli XL1 blue transformed with F59+F54, F59+F55, F59+F56, F59+F57, F59+F58, F42+F51 and F52+F53

Investigator: Florian, Rosario, Louise, Jeff

Aim of the experiment: Transformation of E. coli XL1 blue transformed with F59+F54, F59+F55, F59+F56, F59+F57, F59+F58, F42+F51 and F52+F53.

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 10 µl of DNA was added to 200 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • The cell suspensions were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellets were resuspended in 100 µl of LB-medium and these concentrated cell suspensions were plated again on plates containing antibiotics.

Picking of of E. coli XL1 blue transformed with BBa_K365001 (PIF6), BBa_K729004 (Nuclease from Staphylococcus aureus), BBa_K648011 (XylE RFC25), BBa_J61032 (Alkaline phosphotase), BBa_K426020 (BBa_K426020)

Investigator: Rosario, Florian, Louise, Jeff

Aim of the experiment: Picking of of E. coli XL1 blue transformed with BBa_K365001 (PIF6), BBa_K729004 (Nuclease from Staphylococcus aureus), BBa_K648011 (XylE RFC25), BBa_J61032 (Alkaline phosphotase), BBa_K426020 (BBa_K426020).

Procedure:

  • Picked pipette tips was transferred into cell-culture tubes with air-permeable, sterile cover. Each tube contain 4 mL of LB-medium + 4 µL chloramphenicol(1000x) or ampicillin(1000x).
  • 2 colonies of each plate were picked.
  • These tubes were transferred in a cell culture shaker at 37 °C and were incubated overnight.

Thursday, June 6th

Miniprep of overnight cultures of transformated E. coli XL1 blue with P39, P20, genesynthesis 1&2 and BBa_J61032, BBa_K426020, BBa_K729004, BBa_K365001, BBa_K648011

Investigator: Ingmar

Aim of the experiment:Miniprep of overnight cultures of transformated E. coli XL1 blue with P39, P20, genesynthesis 1&2 and BBa_J61032, BBa_K426020, BBa_K729004, BBa_K365001, BBa_K648011

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
  • The resulting DNA were eluted in tubes labeled as follows:
Content New Tube
P39P184
P39P185
P20P186
P20P187
BBa_J61032P188
BBa_J61032P189
BBa_K426020P190
BBa_K426020P191
BBa_K729004P192
BBa_K729004P193
BBa_K365001P194
BBa_K365001P195
BBa_K648011P196
BBa_K648011P197
Genesynthesis 2P198
Genesynthesis 2P199
Genesynthesis 1P200
Genesynthesis 1P201

Analytical digestion and gelelectrophoresis of P188-P197 (latest received biobricks: BBa_J61032, BBa_K426020, BBa_K729004, BBa_K365001, BBa_K648011)

Investigator: Leonie, Jeff

Aim of the experiment: Analytical digestion and gelelectrophoresis of P188-P197 (latest received biobricks: BBa_J61032, BBa_K426020, BBa_K729004, BBa_K365001, BBa_K648011).

Procedure:

volume reagent
2 µl CutSmart Buffer (10x)
0.25 µl EcoRI-HF
0.25 µl SpeI-HF
15 µl ddH2O
2.5 µl Plasmid
=20 µl TOTAL

Mastermix (12x)

volume reagent
24 µl CutSmart Buffer (10x)
3 µl EcoRI-HF
03 µl SpeI-HF
180 µl ddH2O
=210 µl TOTAL
  • 17.5 µl Mastermix + 2.5 µl Plasmid each
  • Incubation for 90 min at 37 °C.
  • Analytical gelelectrophoresis was performed at 90 V


TUM13 20130606 anal Verd P188-P197 EcoRI.SpeI.png

1 kb Marker P188 Alk.Phos. P189 Alk.Phos. P190 self lysis device P191 self lysis device P192 Nuclease P193 Nuclease P194 PIF6 P195 PIF6 P196 RBS P197 RBS
successful successful successful successful successful successful successful successful successful successful

Picking of of E. coli XL1 blue transformed with the ligation products of F52+F53, F59+F58, F59+F54, F59+F55, F59+F57 and F59+F56

Investigator: Ingmar

Aim of the experiment: Picking of of E. coli XL1 blue transformed with the ligation products of F52+F53, F59+F58, F59+F54, F59+F55, F59+F57 and F59+F56

Procedure:

  • The picked colonies were transferred into cell-culture tubes with air-permeable, sterile cover containing 4 mL of LB-medium + 4 µL chloramphenicol(1000x) or ampecillin (1000x).
  • 2 colonies of each agar plate were picked.
  • These tubes were transferred in a cell culture shaker at 37 °C and were incubated overday.
  • The ligation of F42 and F51 was not successful and has to be repeated. One reason for the failure could be secondary structures of the promoter. Therefore the new ligation batch should be heated to 95°C for a while before adding the T4 ligase.

PCR of P192 (Thermonuclease, O64 & O65) and P194 (PIF6, O42 & O43)

Investigator: Jeff

Aim of the experiment: PCR of P192 (Thermonuclease, O64 & O65) and P194 (PIF6, O42 & O43).

Procedure:

Operational sequence:

  • PCR reaction mixture
volume reagent
10 µl 5x OneTaq Standard Reaction Buffer
1 µl 10 mM dNTPs
1 µl 10 µM Forward Primer (P192: O64 (NucA_fw); P194: O42 (PIF6_fw))
1 µl 10 µM Reverse Primer (P192: O65 (NucA_rv); P194: O43 (PIF6_rv))
0.25 µL OneTaq Hot Start DNA Polymerase (Finally: 1.25 units/50 µL)
1 µl 1:1000 dilution of plasmid DNA (P192; P194)
35.75 µL ddH2O Water
=50 µL TOTAL
  • Mix with pipette
  • The gradient PCR program was performed after following scheme with following conditions:
Initial denaturation 94 °C 30 s
30 cycles 94 °C 30 s
55 °C 60 s
68 °C 30 s
Final extension 68 °C 5 min
Hold 4 °C infinite
  • After PCR, the product was purified with QIAquick PCR Purification Kit, Qiagen.
  • PCR product of P192 = F61; PCR product of 194 = F62

QuikChange mutagenesis to remove forbidden restriction sites - SDMIV - of P179 (Laccase)

Investigator: Jeff

Aim of the experiment: Removal of forbidden restiction site from P179 (Laccase).

Procedure: Quickchange - PCR

Reaction batch

volume reagent Additional information
2.5 µl 10x Pfu Ultra II buffer
0.5 µl Plasmid template (P179 - 1:10 dilution) need to get between 2.5 ng and 25 ng for a reaction batch of 25 µl
1 µl 1:10 dilution of O32 (10 µM)
1 µl 1:10 dilution of O33 (10 µM)
18.5 µl ddH2O
1 µl dNTP mix 50 mM
0.5 µl Pfu Ultra II DNA polymerase (2.5 U/µl)


PCR cycling parameters - P179

Segment Cycles Temperature Time
1 1 95 °C 30 s
2 19 95 °C 30 s
52 °C 1 min
68 °C 4 min
4 °C hold

After the PCR; 1 µl of Dpn1 was added and the reaction mixture was incubated at 37°C for one hour

Analytical gelelectrophoresis of F61 (PCR product of P192, Thermonuclease), F62 (PCR product of P194, PIF6) and the DpnI digestion of the SDMIV product of P179

Investigator: Rosario, Andi, Jeff

Aim of the experiment: Analytical gelelectrophoresis of F61 (PCR product of P192, Thermonuclease), F62 (PCR product of P194, PIF6) and the DpnI digestion of the SDMIV product of P179.

Procedure:

  • 4 µl of F61 or F62 or the DpnI digestion of the SDMIV product of P179 were mixed with 0.444 µl of DNA loading buffer (10x)
  • Analytical gelelectrophoresis was performed at 90 V for 1 h on a 1% agarose gel.

TUM13 20130606 PCR F61 F62 QCIV- P179.png

1 kbp DNA ladder PCR product F61 PCR product F62 DpnI digestion of QCIV of P179
successful successful successful

Ligation of F42+F51

Investigator: Ingmar

Aim of the experiment: Ligation of F42+F51.

Procedure:

  • Ligation batch for F42+F51:
volume reagent
0.68 µl F42 (73.5 ng/µl, 2070 bp)
15.64 µl F51 (10.93 ng/µl, 1237 bp)
5.39 µl ddH2O
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
=20 µl TOTAL
  • Negative control was also prepared. Instead of the insert, the same volume of ddH2O was added to the reaction batch.
  • The reaction batch was heated up to 95°C for 5 min before the enzyme and buffer were added.
  • The ligation was performed for two hours at room temperature.
  • Lid temperature = 37 °C

Transformation of E. coli XL1 blue with F42+F51 (pActin in pSB1C3 RFC10) and DpnI digestion of the SDMIV product of P179 (Laccase)

Investigator: Katrin

Aim of the experiment: Transformation of E. coli XL1 blue with F42+F51 (pActin in pSB1C3 RFC10 )and DpnI digestion of the SDMIV product of P179 (Laccase).

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 10 µl of DNA was added to 200 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • The cell suspensions were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellets were resuspended in 100 µl of LB-medium and these concentrated cell suspensions were plated again on plates containing antibiotics (CamR).

Sequencing of Biobricks P188/189 (alk.Phos., 1475 bp), P190/191 (self lysis device, 2910 bp), P192/193 (Nuclease, 561 bp), P194/195 (PIF6, 300 bp), P196/197 (RBS, 918 bp)

Investigators: Leonie

Aim of the experiment: Sequencing of the Biobrick MiniPreps

Procedure: Peparation of DNA for sequencing according to the Eurofins SmartSeq Kit protocol (15 µl of plasmid DNA (50 - 100 ng/µl) and 2 µl sequencing primer 10 µM):


Label Konz. ng/µl Vol. BB µl Vol H2O µl
P188 160.6 5 10
P189 123.6 7.5 7.5
P190 319.2 3 12
P191 127.0 10 5
P192 336.9 3 12
P193 230.6 4 11
P194 156.6 5 10
P195 197.4 4 11
P196 90.3 10 5
P197 230.2 4 11


The different genes received the following barcodes:

Label Name Barcode1 Barcode2
P188 alk.Phos. FR01002327 (O3) FR01002326 (O4)
P189 alk.Phos. FR01002325 (O3) FR01002320 (O4)
P190 self lysis device FR01002319 (O3) FR01002318 (O4)
P191 self lysis device FR01002317 (O3) FR01002316 (O4)
P192 Nuclease FR01002315 (O3) - (O4)
P193 Nuclease FR01002314 (O3) - (O4)
P194 PIF6 FR01002313 (O3) - (O4)
P195 PIF6 FR01002312 (O3) - (O4)
P196 RBS FR01002324 (O3) FR01002323 (O4)
P197 RBS FR01002322 (O3) FR01002321 (O4)

Preparative digestion and gelelectrophoresis of F61 (Thermonuclease), F62 (PIF6) , P165 (t35S), F31 (miniMCSII)

Investigator: Rosario, Andi, Florian, Johanna, Jeff

Aim of the experiment: Preparative digestion and gelelectrophoresis of F61 (Thermonuclease), F62 (PIF6) , P165 (t35S), F31 (miniMCSII.

Procedure:

  • Batch for preparative digestion of F61 (Thermonuclease) with XbaI & AgeI:
volume reagent
25 µl PCR product F61
5 µl CutSmart Buffer
1 µl XbaI(20 U/µl)
1 µl AgeI-HF (20 U/µl)
18 µl ddH2O
=50 µl TOTAL
  • Batch for preparative digestion of F62 (PIF6) with XbaI & AgeI:
volume reagent
25 µl PCR product F62
5 µl CutSmart Buffer
1 µl XbaI(20 U/µl)
1 µl AgeI-HF (20 U/µl)
18 µl ddH2O
=50 µl TOTAL
  • Batch for preparative digestion of P165 (t35S) with XbaI:
volume reagent
20 µl Plasmid DNA P165
4 µl CutSmart Buffer
1 µl XbaI (20 U/µl)
15 µl ddH2O
=40 µl TOTAL
  • Batch for preparative digestion of F31 (miniMCSII):
volume reagent
10 µl Oligohybridization F31
5 µl CutSmart Buffer
1 µl SpeI-HF (20 U/µl)
34 µl ddH2O
=40 µl TOTAL
  • Incubation for 3 h at 37 °C.
  • 5 µl of DNA loading buffer (10x) were added to the 50 µl reaction batches and 4 µl of DNA loading buffer (10x) were added to the 40 µl reaction batches after digestion and were loaded on an 2% agarose gel for preparative gelelectrophoresis (1% agarose gel for digestion of P165).
  • Preparative gelelectrophoresis was performed at 90 V for 60 min.

TUM13 20130606 prep Verd F31 SpeI F61 XbaI.AgeI F62 XbaI.AgeI.png

1 kbp DNA ladder Digestion of F31 with SpeI-HF Digestion of F61 with XbaI & AgeI-HF Digestion of F62 with XbaI & AgeI-HF
Fragment length as expected; band was cut out Fragment length as expected; band was cut out Fragment length as expected; band was cut out


TUM13 20130606 prep Verd P165 XbaI.png


1 kbp DNA ladder Digestion of P165 with XbaI
Fragment length as expected; band was cut out
  • Bands were extracted by QIAquick Gel Extraction Kit, QIAGEN.

Dephosphorylation of preparative digestion of P165 with FastAP

Investigator: Rosario, Jeff

Aim of the experiment: Dephosphorylation of preparative digestion of P165 with FastAP to prevent re-ligation.

Procedure:

  • After preparative digestion, gelelectrophoresis and gelextraction of P165, the digestion product was purified with QIAquick PCR Purification Kit, Qiagen.
  • Batch for the dephosphorylation of digestion product of P165
volume reagent
30 µl Digestion product of P165
4 µl 10X Fast AP buffer
2 µl FastAP Thermosensitive Alkaline Phosphatase
4 µl ddH2O
=40 µl TOTAL
  • The reaction batch was spun briefly and incubated at 37 °C for 10 min.
  • The reaction was stopped by heating to 75 °C for 5 min.
  • The dephosphorylized digestion product of P165 product was purified with QIAquick PCR Purification Kit, Qiagen.
  • The resulting product was labelled as F63

Ligation of F58+F59, F55+F59, F54+F59, F56+F59, F57+F59, F52+F53, F42+F51

Investigator: Jeff, Rosario

Aim of the experiment: Ligation of F53+F59, F58+F59, F55+F59, F54+F59, F56+F59, F57+F59, F52+F53, F42+F51.

Procedure:

  • Ligation batch for F59+F65 (Thermonuclease in pSB1C3 RFC25):
volume reagent
1.5 µl F59 (66.7 ng/µl, 2086 bp)
4.56 µl F65 (14.1 ng/µl, 447 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
10.94 µl ddH2O
=20 µl TOTAL
  • Ligation batch for F59+F66:
volume reagent
1.5 µl F59 (66.7 ng/µl, 2086 bp)
3.78 µl F66 (11.3 ng/µl, 297 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
11.72 µl ddH2O
=20 µl TOTAL
  • Ligation batch for F63+F64:
volume reagent
12.05 µl F63 (8.3 ng/µl, 2287 bp)
4.95 µl F64 (4.3 ng/µl, 22 bp)
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
=20 µl TOTAL
  • Negative control was also prepared. Instead of the insert, the same volume of ddH2O was added to the reaction batch.
  • Ligation was performed at 16 °C overnight.

Friday, June 7th

Picking of QC IV Laccase

Investigator: Johanna

Aim of the study: Picking of QC IV Laccase (concentrated) and QC IV Laccase (diluted)

Operational sequence:

  • Picking and overnight culture after standard laboratory's protocol. (4 µl CamR and 4 ml LB-medium)
  • 3 colonies were picked for every Transformation product.

Preparation of Knop-Medium for Moss

Investigator: Andi

Aim of the experiment: Preparation of Knop-Medium for Moss

Procedure:

  • All four prepared stocks have been: 25g/L KH2PO4; 25g/L KCl; 25g/L MgSO4 x 7 H2O; 100g/L Ca(NO3)2
  • Volume of prepared Medium: 2.6L
  • 10 ml of each stock were converted into a 5L Erlenmeyer flask and filled up to 2.6L with destilled water (ELGA); 32.5mg FeSO4 x 7 H2O were added; the pH was set to 5.8 with KOH/NaOH
  • 200ml of the prepared medium was filled into three 500ml Erlenmeyer flasks, so each Erlenmeyer flask contained 200 ml of the Knop-Medium; the rest (2L) was left in the 5L EM flask
  • All flasks have been autoclaved

Miniprep of overnight cultures of transformated E. coli XL1 blue with F52+F53, F59+F54, F59+F55, F59+F56, F59+F57, F59+F58

Investigator: Rosario

Aim of the experiment:Miniprep of overnight cultures of transformated E. coli XL1 blue with F52+F53, F59+F54, F59+F55, F59+F56, F59+F57, F59+F58

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
  • The resulting DNA were eluted in tubes labeled as follows:
Content New Tube
F52+F53 IP202
F52+F53 II203
F59+F54 IP204
F59+F54 IIP205
F59+F55 IP206
F59+F55 IIP207
F59+F56 IP208
F59+F56 IIP209
F59+F57 IP210
F59+F57 IIP211
F59+F58 IP212
F59+F58 IIP213


Transformation of E. coli XL1 blue with F59 + F65 (Thermonuclease in pSB1C3), F59 + F66 (PIF6 in pSB1C3) and F63 + F64 (MiniMCS + t35S in pSB1C3)

Investigator: Florian

Aim of the experiment: Transformation of E. coli XL1 blue with F59 + F65 (Thermonuclease in pSB1C3), F59 + F66 (PIF6 in pSB1C3) and F63 + F64 (MiniMCS + t35S in pSB1C3).

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 10 µl of ligation product were added to 200 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • 100 µl of each tube were plated on agarose plates containing antibiotics (CamR).
  • The cell suspensions were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellets were resuspended in 100 µl of LB-medium and these concentrated cell suspensions were plated again on plates containing antibiotics (CamR).

Sequencing of P204 (Ligation Product F59+F54), P206 (Ligation Product F59+F55), P208 (Ligation Product F59+F56), P210 (Ligation Product F59+F57), P212 (Ligation Product F59+F58)

A monster is born!

Investigators: Louise

Aim of the experiment: Sequencing of Ig-Kappa (P204), Nanoluciferase (P206), SigP (P208), Transmembrand. (P210) and SpyCatcher (P212) Ligations in pSB1C3 RFC25

Procedure: The DNA was prepared for sequencing according to the Eurofins SmartSeq Kit protocol (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer).

The different genes we sequenced received the following barcodes:

Label Name Barcode (O3)
P204 Ig-Kappa + pSB1C3 RFC25 FR01002304
P206 Nanoluciferase + pSB1C3 RFC25 FR01002303
P208 SigP + pSB1C3 RFC25 FR01002302
P210 Transmembrand + pSB1C3 RFC25 FR01002301
P212 SpyCatcher + pSB1C3 RFC25 FR01002300

Analytical digestion and gelelectrophoresis of P202-P213

Investigator: Katrin

Aim of the experiment: Analytical digestion and gelelectrophoresis of P202-P213

Procedure:

  • Mastermix for analytical digestion of P202-P213 with XbaI+AgeI
volume reagent
30 µl CutSmart Buffer (10x)
3.75 µl XbaI
3.75 µl SpeI-HF
225 µl ddH2O
=262.5 µl TOTAL
  • 17.5 µl of the mastermix was added to 2.5 µl of plasmid DNA (P202-P203)
  • Incubation for 90 min at 37 °C.
  • Inaddition, P203 was digested for 4 and for 8 seconds in the microwave, a negative control was incubated at room temperature
  • Analytical gelelectrophoresis was performed at 90 V for 60 min.


TUM13 20130607 anal Verd P202-P210 XbaI.AgeI.png


1 kbp ladder DNA ladder Digestion of P202 with XbaI und AgeI (GFP + linker) Digestion of P203 with XbaI und AgeI (GFP + linker) Digestion of P204 with XbaI und AgeI Digestion of P205 with XbaI und AgeI Digestion of P206 with XbaI und AgeI Digestion of P207 with XbaI und AgeI Digestion of P208 with XbaI und AgeI Digestion of P209 with XbaI und AgeI Digestion of P210 with XbaI und AgeI
as expected as expected not as expected not as expected not as expected not as expected not as expected not as expected not as expected as expected (SERK-TMD)


[[File:|500px]]

1 kbp ladder DNA ladder Digestion of P211 with XbaI und AgeI Digestion of P212 with XbaI und AgeI Digestion of P213 with XbaI und AgeI Digestion of P203 with XbaI und AgeI (microwave 4 seconds) Digestion of P203 with XbaI und AgeI (microwave 8 seconds) Digestion of P203 with XbaI und AgeI (control)
as expected (SERK-TMD) not as expected not as expected not as expected interesting interesting interesting

Saturday, June 8th

Miniprep of overnight cultures of transformated E. coli XL1 blue QC IV Laccase

Investigator: Rosario

Aim of the experiment:Miniprep of overnight cultures of transformated E. coli XL1 blue QC IV Laccase

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
  • The resulting DNA were eluted in tubes labeled as follows:
Content New Tube
QC IV Laccase clone 1P214
QC IV Laccase clone 2P215
QC IV Laccase clone 3P216
QC IV Laccase clone 4P217
QC IV Laccase clone 5P218
QC IV Laccase clone 6P219

Picking of F59 + F65 (Thermonuclease in pSB1C3), F59 + F66 (PIF6 in pSB1C3) and F63 + F64 (MiniMCS + t35S in pSB1C3)

Investigator: Rosario

Aim of the study: Picking of F59 + F65 (Thermonuclease in pSB1C3), F59 + F66 (PIF6 in pSB1C3) and F63 + F64 (MiniMCS + t35S in pSB1C3) Operational sequence:

  • Picking and overnight culture after standard laboratory's protocol. (4 µl CamR and 4 ml LB-medium)
  • 2 colonies were picked for every Transformation product.


Preparative digestion and gelelectrophoresis of F47 (pActin, fragment named F68) with XbaI/SpeI, P202 (GFP+linker, fragment named F69) with NgoMIV/SpeI, P210 (SERK-TMD, fragment named F67)

Investigator: Jeff, Leonie, Katrin

Aim of the experiment: Preparative digestion and gelelectrophoresis of F47 (pActin, fragment named F68) with XbaI/SpeI, P202 (GFP+linker, fragment named F69) with NgoMIV/SpeI, P210 (SERK-TMD, fragment named F67) with AgeI/SpeI

Procedure:

  • Batch for preparative digestion of F47 (pActin, fragment named F68) with XbaI/SpeI
volume reagent
25 µl PCR product F47
5 µl CutSmart Buffer
1 µl XbaI(20 U/µl)
1 µl SpeI-HF (20 U/µl)
18 µl ddH2O
=50 µl TOTAL
  • Batch for preparative digestion of P202 (GFP+linker, fragment named F69) with NgoMIV/SpeI
volume reagent
20 µl plasmid P202
5 µl CutSmart Buffer
1 µl SpeI-HF(20 U/µl)
1 µl NgoMIV (20 U/µl)
23 µl ddH2O
=50 µl TOTAL
  • Batch for preparative digestion of P210 (SERK-TMD, fragment named F67) with AgeI/SpeI
volume reagent
20 µl Plasmid DNA P210
5 µl CutSmart Buffer
1 µl AgeI-HF (20 U/µl)
1 µl SpeI-HF (20 U/µl)
23 µl ddH2O
=50 µl TOTAL


  • Incubation for 3 h at 37 °C.
  • 5 µl of DNA loading buffer (10x) were added to the 50 µl reaction batches after digestion and were loaded on a 1% agarose gel for preparative gelelectrophoresis
  • Preparative gelelectrophoresis was performed at 90 V for 60 min.

TUM13 20130608 prep Verd F47 XbaI.SpeI.png

1 kbp DNA ladder digestion of F47 (pActin, fragment named F68) with XbaI/SpeI
Fragment length as expected; band was cut out


TUM13 20130608 prep Verd P202 NgoMIV.SpeI.png


1 kbp DNA ladder digestion of P202 (GFP+linker, fragment named F69) with NgoMIV/SpeI
Fragment length as expected; band was cut out


TUM13 20130608 prep Verd P210 AgeI.SpeI.png


1 kbp DNA ladder digestion of P210 (SERK-TMD, fragment named F67) with AgeI/SpeI
Fragment length as expected; band was cut out


  • Bands were extracted by QIAquick Gel Extraction Kit, QIAGEN.
  • Concentration determined with Nanodrop:
F68 pActin 10,4 ng/µl
F69 GFP+linker 13,0 ng/µl
F67 SERK-TMD 14,3 ng/µl

Preparative digestion and gelelectrophoresis of P7 (PhyB in pSB1C3, fragment named F75) with XbaI/SpeI and P8 (PhyB in pSC1C3, fragment named F76) with NgoMIV/SpeI

Investigator: Jeff, Leonie, Katrin

Aim of the experiment: Preparative digestion and gelelectrophoresis of P7 (PhyB in pSB1C3, fragment named F75) with XbaI/SpeI and P8 (PhyB in pSC1C3, fragment named F76) with NgoMIV/SpeI (backbones for ligation)

Procedure:

  • Batch for preparative digestion of P7 (PhyB in pSB1C3, fragment named F75) with XbaI/SpeI
volume reagent
20 µl Plasmid P7
5 µl CutSmart Buffer
1 µl XbaI(20 U/µl)
1 µl SpeI-HF (20 U/µl)
23 µl ddH2O
=50 µl TOTAL
  • Batch for preparative digestion of P8 (PhyB in pSC1C3, fragment named F76) with NgoMIV/SpeI
volume reagent
20 µl plasmid P8
5 µl CutSmart Buffer
1 µl SpeI-HF(20 U/µl)
1 µl NgoMIV (20 U/µl)
23 µl ddH2O
=50 µl TOTAL
  • Incubation for 3 h at 37 °C.
  • before gelelectrophoresis, P7 was dephosphorylated
  • 5 µl of DNA loading buffer (10x) were added to the 50 µl reaction batches after digestion and were loaded on a 0.5% agarose gel for preparative gelelectrophoresis
  • Preparative gelelectrophoresis was performed at 90 V for 60 min.

TUM13 20130608 prep Verd P7 XbaI.SpeI P8 NgoMIV.SpeI.png

1 kbp DNA ladder digestion of P7 (PhyB in pSB1C3, fragment named F75) with XbaI/SpeI digestion of P8 (PhyB in pSC1C3, fragment named F76) with NgoMIV/SpeI
Fragment lengths as expected; lower band was cut out Fragment lengths as expected; lower band was cut out


  • Bands were extracted by QIAquick Gel Extraction Kit, QIAGEN.
  • Concentration determined with Nanodrop:
F75 dephosphorylated Backbone (P7) 39,4 ng/µl
F76 dephosphorylated Backbone (P8) 52,0 ng/µl



Dephosphorylation of F75

Investigator: Jeff, Leonie, Katrin

Aim of the experiment: Dephosphorylation of cut vector pSB1C3 prevent re-ligation

Procedure:

  • the digestion product was purified with QIAquick PCR Purification Kit, Qiagen in order to change the buffer
  • Batch for the dephosphorylation of F75
volume reagent
30 µl Plasmid DNA F75 from digestion
3 µl 10X Fast AP buffer
1.3 µl FastAP Thermosensitive Alkaline

Phosphatase

=34.3 µl TOTAL
  • the reaction batch was spun briefly and incubated at 37 °C for 10 minutes
  • the reaction was stopped by heating to 75 °C for 5 minutes

Preparative digestion and gelelectrophoresis of P200 (gene synthesis 1, fragments named F70+F71) with XbaI/AgeI and P198 (gene synthesis 2, fragments named F72-F74) with XbaI/AgeI

Investigator: Jeff, Leonie, Katrin

Aim of the experiment: Preparative digestion and gelelectrophoresis of P200 (gene synthesis 1, fragments named F70+F71) with XbaI/AgeI and P198 (gene synthesis 2, fragments named F72-F74) with XbaI/AgeI

Procedure:

  • Batch for preparative digestion of P200 (gene synthesis 1, fragments named F70+F71) with XbaI/AgeI
volume reagent
20 µl Plasmid P7
5 µl CutSmart Buffer
1 µl XbaI(20 U/µl)
1 µl AgeI-HF (20 U/µl)
23 µl ddH2O
=50 µl TOTAL
  • Batch for preparative digestion of P198 (gene synthesis 2, fragments named F72-F74) with XbaI/AgeII
volume reagent
20 µl Plasmid P7
5 µl CutSmart Buffer
1 µl XbaI(20 U/µl)
1 µl AgeI-HF (20 U/µl)
23 µl ddH2O
=50 µl TOTAL
  • Incubation for 3 h at 37 °C.
  • 5 µl of DNA loading buffer (10x) were added to the 50 µl reaction batches after digestion and were loaded on a 2% agarose gel for preparative gelelectrophoresis
  • Preparative gelelectrophoresis was performed at 90 V for 60 min.

TUM13 20130608 prep Verd P200 P198 AgeI.XbaI.png

1 kbp DNA ladder digestion of P200 (gene synthesis 1, fragments named F70+F71) with XbaI/AgeI digestion of P198 (gene synthesis 2, fragments named F72-F74) with XbaI/AgeII
Fragment lengths as expected; the two lower bands were cut out (upper:F70, lower: F71) Fragment lengths as expected; all bands were cut out (upper: F72, middle: F73, lower: F74)


  • Bands were extracted by QIAquick Gel Extraction Kit, QIAGEN.
  • Concentrations measured with Nano-Drop
Fragment Name Length Concentration
F70 Nanoluciferase 510 bp 9.2 ng/µl
F71 IgKappa-SigP 67 bp 3.1 ng/µl
F72 SpyCatcher 339 bp 10.8 ng/µl
F73 SERK-TMD 186 bp 8.6 ng/µl
F74 SERK-SigP 100 bp 4.8 ng/µl


Analytical digestion and gelelectrophoresis of P214-219 (Miniprep of Laccase QC IV), P179 (control before QC IV)

Investigator: Jeff, Leonie, Katrin

Aim of the experiment: Analytical digestion and gelelectrophoresis of P214-219 (Miniprep of Laccase QC IV), P179 (control before QC IV)

Procedure:

  • Mastermix for analytical digestion of P214-219 (Miniprep of Laccase QC IV), P179 (control before QC IV)


  • 17.5 µl of the mastermix was added to 2.5 µl of plasmid DNA (P214-219, P179)
  • Incubation for 90 min at 37 °C.
  • digestion for 4 x 10 seconds in the microwave (600 watt), with two minute breaks in between the microwaving
  • Analytical gelelectrophoresis was performed at 90 V for 60 min.


TUM13 20130608 anal Verd microwave P214-219,P179 NgoMVI.AgeI.png

1 kbp DNA ladder digestion of P214 (Miniprep of Laccase QC IV clone 1) with NgoMVI/AgeI digestion of P215 (Miniprep of Laccase QC IV clone 2) with NgoMVI/AgeI digestion of P216 (Miniprep of Laccase QC IV clone 3) with NgoMVI/AgeI digestion of P217 (Miniprep of Laccase QC IV clone 4) with NgoMVI/AgeI digestion of P218 (Miniprep of Laccase QC IV clone 5) with NgoMVI/AgeI digestion of P219 (Miniprep of Laccase QC IV clone 6) with NgoMVI/AgeI digestion of P179 (Miniprep of ligation product Laccase QCIII clone 2) with NgoMVI/AgeI
as expected as expected as expected as expected as expected as expected as expected

Ligation of F75+F69 (Linker+GFP into pSB1C3) and F67+F69 (Linker+GFP into TMD-pSB1C3-Suffix)

Investigator: Jeff, Leonie Aim of the experiment: Ligation of F75+F69 (Linker+GFP into pSB1C3) and F67+F69 (Linker+GFP into TMD-pSB1C3-Suffix)

Procedure:

volume reagent
2.54 µl F75 (39.4 ng/µl, ? bp)
8.30 µl F69 (13.0 ng/µl, ? bp)
6.16 µl ddH2O
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl) =20 µl TOTAL


volume reagent
7.00 µl F67 (14.3 ng/µl, ? bp)
7.62 µl F69 (13.0 ng/µl, ? bp)
2.38 µl ddH2O
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
TOTAL
  • Incubation: 1 h 22°C


Transformation of E. coli XL1 blue with F75+F69(Linker+GFP into pSB1C3) and F67+F69 (Linker+GFP into pSB1C3-TMD-Suffix)

Investigator: Jeff, Leonie

Aim of the experiment: Transformation of E. coli XL1 blue with F75+F69(Linker+GFP into pSB1C3) and F67+F69 (Linker+GFP into pSB1C3-TMD-Suffix)

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 10 µl of DNA was added to 200 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • The cell suspensions were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellets were resuspended in 100 µl of LB-medium and these concentrated cell suspensions were plated again on plates containing antibiotics (CamR).

Sunday, June 9th

Miniprep of overnight cultures of transformated E. coli XL1 blue of F59+F65 (Nuclease), F59+F66 (PIF6), F59+F54 (Ig-K), F59+F55 (Luciferase), F59+F56 (SigP), F59+F57 (SERK-TMD), F59+F58 (SpyCatcher), F42+F51 (pActin), F63+F64

Investigator: Katrin

Aim of the experiment:Miniprep of overnight cultures of transformated E. coli XL1 blue of F59+F65 (Nuclease), F59+F66 (PIF6), F59+F54 (Ig-K), F59+F55 (Luciferase), F59+F56 (SigP), F59+F57 (SERK-TMD), F59+F58 (SpyCatcher), F42+F51 (pActin), F63+F64

Procedure:

  • Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
  • The resulting DNA were eluted in tubes labeled as follows:
Content New Tube
F59+F65 clone 1P220
F59+F65 clone 2P221
F59+F66 clone 1P222
F59+F66 clone 2P223
F59+F56 clone 1P224
F59+F56 clone 2P225
F59+F55 clone 1P226
F59+F55 clone 2P227
F59+F57 clone 1P228
F59+F57 clone 2P229
F59+F58 clone 1P230
F59+F58 clone 2P231
F63+F64 P232
F42+F51 P233
F59+F54 clone 1P234
F59+F54 clone 2P235

Analytical digestion and gelelectrophoresis of P220-P235 ((P220-231, P233-P235 with XbaI/SpeI, P232 with MfeI/Pst1)

Investigator: Katrin

Aim of the experiment: Analytical digestion and gelelectrophoresis of P220-P235 (Minipreps)

Procedure:

  • Mastermix for analytical digestion of P220-231, P233-P235 with XbaI, SpeI
volume reagent
34 µl CutSmart Buffer
4.25 µl XbaI(20 U/µl)
4.25 µl SpeI-HF (20 U/µl)
255 µl ddH2O
=266.5 µl TOTAL
  • 17.5 µl of the mastermix was added to 2.5 µl of plasmid DNA
  • reaction batch for analytical digestion of P232 with MfeI/PstI
volume reagent
2.5 µl P232
2 µl CutSmart Buffer
0.25 µl MfeI(20 U/µl)
0.25 µl PstI-HF(20 U/µl)
15 µl ddH2O
=20 µl TOTAL


  • Incubation for 60 min at 37 °C.
  • Analytical gelelectrophoresis was performed at 90 V for 60 min
  • for P224, P225, P228, P229, P230, P231, P234, P235,a 2% agarose gel was used, gelelectrophoresis was performed at 90 V for 45 min

20130609 anal Verd P220,221,222,223,226,227 XbaI.SpeI P232 MfeI.PstI P233 XbaI.SpeI.png

1 kbp DNA ladder 100 bp DNA ladder digestion of P224 (SigP, clone 1) with XbaI, SpeI digestion of P225 (SigP, clone 2) with XbaI, SpeI digestion of P228 (SERK TMD, clone 1) with XbaI, SpeI digestion of P229 (SERK TMD, clone 2) with XbaI, SpeI digestion of P230 (SpyCatcher, clone 1) with XbaI, SpeI digestion of P231 (SpyCatcher, clone 2) with XbaI, SpeI digestion of P234 (Ig-K, clone 1) with XbaI, SpeI digestion of P235 (Ig-K, clone 2) with XbaI, SpeI
not as expected not as expected as expected as expected as expected as expected fragment not visible due to small size not as expected


20130609 anal Verd P224,225,338,229,230,231,234,235 XbaI.SpeI.png

1 kbp DNA ladder digestion of P220 (Thermonuclease, clone 1) with XbaI, SpeI digestion of P221 (Thermonuclease, clone 2) with XbaI, SpeI digestion of P222 (PIF6, clone 1) with XbaI, SpeI digestion of P223 (PIF6, clone 2) with XbaI, SpeI digestion of P226 (Luciferase, clone 1) with XbaI, SpeI digestion of P227 (Luciferase, clone 2) with XbaI, SpeI digestion of P232 (miniMCS) with MfeI/PstI digestion of P233 (pActin) with XbaI, SpeI
not as expected not as expected as expected as expected as expected as expected not as expected as expected

Picking of F67+F69 (SERK-TMD+linker GFP)

Investigator: Katrin

Aim of the study: Picking of F67+F69 (SERK-TMD+linker GFP)

Operational sequence:

  • Picking and overnight culture after standard laboratory's protocol. (5 µl CamR and 5 ml LB-medium)
  • 3 colonies were picked for every Transformation product.
  • There were no colonies on the plates for ligations F68+F75 (pActin, pSB1C3),

(probably due to dephosphorylation)

Preparative digestion and gelelectrophoresis of P220 (thermonuclease, fragment corrupted) with NgoMIV/SpeI, P160 (NLS, fragment named F77) with AgeI/SpeI, P40 (GSAT linker, fragment named F79) with NgoMIV/SpeI, P7 (PhyB, fragment named F78) with AgeI/SpeI

Investigator: Katrin

Aim of the experiment: Preparative digestion and gelelectrophoresis of P220 (thermonuclease, fragment corrupted) with NgoMIV/SpeI, P160 (NLS, fragment named F77) with AgeI/SpeI, P40 (GSAT linker, fragment named F79) with NgoMIV/SpeI, P7 (PhyB, fragment named F78) with AgeI/SpeI

Procedure:

  • Batch for preparative digestion of P220 (thermonuclease, fragment corrupted) with NgoMIV/SpeI
volume reagent
20 µl P220
5 µl CutSmart Buffer
1 µl NgoMIV(20 U/µl)
1 µl SpeI-HF (20 U/µl)
14 µl ddH2O
=40 µl TOTAL
  • Batch for preparative digestion of P160 (NLS, fragment named F77) with AgeI/SpeI
volume reagent
20 µl plasmid P160
5 µl CutSmart Buffer
1 µl SpeI-HF(20 U/µl)
1 µl AgeI-HF (20 U/µl)
14 µl ddH2O
=40 µl TOTAL
  • Batch for preparative digestion of P40 (GSAT linker, fragment named F79) with NgoMIV/SpeI
volume reagent
20 µl plasmid P40
5 µl CutSmart Buffer
1 µl SpeI-HF(20 U/µl)
1 µl NgoMIV (20 U/µl)
14 µl ddH2O
=40 µl TOTAL
  • Batch for preparative digestion of P7 (PhyB, fragment named F78) with AgeI/SpeI
volume reagent
20 µl plasmid P40
5 µl CutSmart Buffer
1 µl SpeI-HF(20 U/µl)
1 µl AgeI-HF (20 U/µl)
14 µl ddH2O
=40 µl TOTAL
  • Incubation for 2 h at 37 °C.
  • 4 µl of DNA loading buffer (10x) were added to the 40 µl reaction batches containing P220 and P40 after digestion and were loaded on a 1% agarose gel for preparative gelelectrophoresis
  • the vector backbones where only a few base pairs were cut out were purified via PCR-purification
  • Preparative gelelectrophoresis was performed at 90 V for 60 min.

20130609 prep Verd P220, P40 NgoMIV.SpeI.png

digestion of P220 (thermonuclease, fragment corrupted) with NgoMIV/SpeI 1 kbp DNA ladder digestion of P40 (GSAT linker, fragment named F79) with NgoMIV/SpeI
not as expected, band was discarded as expected, lower band (108 bp) was cut out
  • the band was extracted with QIAquick Gel Extraction Kit, QIAGEN.

PCR Purification of vector backbones P7 (PhyB in pSB1C3, fragment F78), P160 (NLS in pSB1C3, fragment F77)

Investigator: Katrin

Aim of the study: PCR Purification of vector backbones P7 (PhyB in pSB1C3, fragment F78), P160 (NLS in pSB1C3, fragment F77)

  • in order to get rid of the few base pairs that were cut out during digestion, the digestion batches were purified 
with QIAquick PCR Purification Kit, Qiagen
  • the yiedls were 56.2 ng/µl for F77 and 277,6 ng/µl for F78

Ligation of F78+F79(PhyB+linker) and F59+F71 (pSB1C3+Ig-K)

Investigator: Katrin Aim of the experiment: Ligation of F78+F79(PhyB+linker) and F59+F71 (pSB1C3+Ig-K)

Procedure:

  • Ligation batch for F78+F79(PhyB+linker)
volume reagent
0.36 µl F78 (277.6 ng/µl, 4807 bp)
1.77 µl P79 (3.8 ng/µl, 108 bp)
14.87 µl ddH2O
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
=20 µl TOTAL
  • Ligation batch for F59+F71 (pSB1C3+Ig-K)
volume reagent
1.5 µl F59 (66.7 ng/µl, 2086 bp)
3.12 µl P71 (3.1 ng/µl, 67 bp)
12.38 µl ddH2O
2 µl T4 ligase buffer (10x)
1 µl T4 ligase (1 U/µl)
=20 µl TOTAL
  • Negative control was also prepared. Instead of the insert, the same volume of ddH2O was added to the reaction batch.
  • The ligation was performed for 1 hour at room temperature.

Transformation of E. coli XL1 blue with F78+F79(PhyB+linker) and F59+F71 (pSB1C3+Ig-K)

Investigator: Katrin

Aim of the experiment: Transformation of E. coli XL1 blue with F78+F79(PhyB+linker) and F59+F71 (pSB1C3+Ig-K) and negative controls F78 and F59

Procedure:

  • CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.
  • 10 µl of DNA was added to 200 µl of competent cells and gently mixed.
  • 30 min incubation on ice
  • 5 min. heat shock at 37 °C
  • Adding of 1 ml LB-medium to each tube.
  • Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker.
  • The cell suspensions were centrifuged for 1 min at 13000 rpm and the supernatant was dicarded.
  • The pellets were resuspended in 100 µl of LB-medium and these concentrated cell suspensions were plated again on plates containing antibiotics (CamR).

PCR of P192 (Thermonuclease, O64 & O65)

Investigator: Katrin

Aim of the experiment: PCR of P192 (Thermonuclease, O64 & O65)

Procedure:

Operational sequence:

  • PCR reaction mixture
volume reagent
10 µl 5x OneTaq Standard Reaction Buffer
1 µl 10 mM dNTPs
1 µl 10 µM Forward Primer O64 (NucA_fw)
1 µl 10 µM Reverse Primer O65 (NucA_rv)
0.25 µL OneTaq Hot Start DNA Polymerase (Finally: 1.25 units/50 µL)
1 µl 1:1000 dilution of plasmid DNA (P192)
35.75 µL ddH2O Water
=50 µL TOTAL
  • Mix with pipette
  • The gradient PCR program was performed after following scheme with following conditions:
Initial denaturation 94 °C 30 s
30 cycles 94 °C 30 s
55 °C 60 s
68 °C 30 s
Final extension 68 °C 5 min
Hold 4 °C infinite

Week 8

Monday, June 10rd

PCR Purification of Thermonuclease (P192)

Investigator: Leonie

Aim of the study: PCR Purification of Thermonuclease (P192)

  • After the PCR the batch was purified with QIAquick PCR Purification Kit, Qiagen
  • the yield was ?? ng/µl for F??

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