Team:Paris Saclay/Notebook/August/30

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Contents

Notebook : August 30

summary

  • check the size by Gel electrophoresis for PCR clonies on Gibson assembly and ligation promoter fnr(repressor) plus RBS_AmilCP+Term_PSB1C3 .
  • Do ligation for For promoter fnr(repressor)+ RBS_LacZ+Term_PSB1C3 , promoter fnr(activator)nirK + RBS_LacZ+Term_PSB3K3 and promoter fnr(repressor) + RBS_LacZ+Term_PSB3K3 and Transformation and

incubation.



lab work


  • A.aero/anaerobic regulation system


1 -Gel electrophoresis of PCR clonies on Gibson assembly .

[[]]
  • Well 1 : 6µL DNA Ladder
  • Well AA 1-8 : Clonies from Gibson FNR_part1, FNR part1 and plasmid PSB1C3
  • Well AB 1-8 : Clonies from Gibson FNR_part1, FNR part1 and plasmid PSB1C3 Concentrate3
  • Well AC 1-8 :Clonies from Gibson RBS_BphR2_part1, BphR2_part2 and plasmid PSB1C3
  • Well AD 1-8 :Clonies from Gibson RBS_FNR part1, FNR_part2 and plasmid PSB1C3
  • Well AE 1-8 :Clonies from Gibson RBS_FNR part1, FNR_part2 and plasmid PSB1C3 Concentrate
  • Well AF 1-8 :Clonies from Gibson RBS_BphR2_part1, BphR2_part2 and plasmid PSB1C3 Concentrate
  • Gel : 1.0%

2 -Gel electrophoresis of ligation promoter fnr(repressor) plus RBS_AmilCP+Term_PSB1C3 .

[[]]
  • Well 0: 6µL DNA Ladder
  • Well 1: clone1 of ligation promoter fnr(repressor) plus RBS_AmilCP+Term_PSB1C3
  • Well 2: clone2 of ligation promoter fnr(repressor) plus RBS_AmilCP+Term_PSB1C3
  • Well 3: clone3 of ligation promoter fnr(repressor) plus RBS_AmilCP+Term_PSB1C3
  • Well 4: clone4 of ligation promoter fnr(repressor) plus RBS_AmilCP+Term_PSB1C3
  • Gel : 1.0%



Ligation


For promoter fnr(repressor)+ RBS_LacZ+Term_PSB1C3  :
promoter fnr(repressor) 8µl
RBS_LacZ+Term 3µl
Ligation buffer 2µl
Ligation T4 enzyme 2µl
H2O 6µl

Transformation theligation and spread in LB plates with Chlorenphenicol and Xgal. incubated at 37°C in aerobic condition over night.

For promoter fnr(activator)nirK + RBS_LacZ+Term_PSB3K3  :


promoter fnr(activator)nirK 3µl
RBS_LacZ+Term 3µl
Plasmid PSB3K3 5µl
Ligation buffer 2µl
Ligation T4 enzyme 1µl
H2O 6µl

Transformation theligation and spread in LB plates with k and Xgal. incubated at 37°C in anaerobic condition over night.


For promoter fnr(repressor) + RBS_LacZ+Term_PSB3K3  :


promoter fnr(repressor) 3µl
RBS_LacZ+Term 3µl
Plasmid PSB3K3 5µl
Ligation buffer 2µl
Ligation T4 enzyme 1µl
H2O 6µl

Transformation theligation and spread in LB plates with k and Xgal. incubated at 37°C in aerobic condition over night.


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Notebook : August 23

Lab work

A - Aerobic/Anaerobic regulation system

Objective : characterize Bba_K1155000, Bba_K1155004, Bba_K1155005, Bba_K1155006

1 - Results of liquid culture of Pfnr-RBS-Amil CP-Term in PSB1C3 in aerobic and anaerobic conditions

XiaoJing

IT WORKS !!!

PsPfnr3008.jpg

In anaerobic conditions, thank to promotor RBS-Amil CP-Term, the dectetion gene is activated and we can see a violet coloration of bacterias.

In aerobic conditions, promotor RBS-Amil CP-Term is inactive, the dectetion gene isn't activated and we can't see any coloration of bacterias.

2 - Results of culture of Pfnr-RBS-Amil CP-Term in PSB1C3, NirB with RBS-LacZ-Term in PSB1C3 in aerobic and anaerobic conditions

XiaoJing

Purification of 08/22/13 didn't work. We have blue colonies for Pfnr with RBS-Amil CP-Term in PSB1C3 in aerobic and anaerobic conditions. We also have blue colonies for NirB with RBS-LacZ-Term in PSB1C3 in anaerobic conditions.

PsPfnrcult3008.jpg PsNirBcult3008.jpg

3 - Ligation of Pfnr with RBS-LacZ-Term in PSB1C3

XiaoJing

Used quantities :

  • Pfnr : 8µL
  • RBS-LacZ-Term in PSB1C3 : 3µL
  • Buffer ligation : 2µL
  • Ligase : 1µL
  • H2O : 6µL

4 - Transformation of ligation of Pfnr with RBS-LacZ-Term in PSB1C3 in DH5α

XiaoJing

Protocol : Bacterial transformation

A - Aerobic/Anaerobic regulation system / B - PCB sensor system

Objective : obtaining FNR and BphR2 proteins

1 - Electrophoresis of Colony PCR of FNR, RBS-FNR and RBS-BphR2

]]
  • Well 1 : 6µL DNA Ladder
  • Well 2 to 17 : 5µL of FNR+1µl of 6X loading dye
  • Well 18 to 26 : 5µL of RBS-BphR2+1µl of 6X loading dye
  • Well 27 : 6µL DNA Ladder
  • Well 28 to 41 : 5µL of RBS-FNR+1µl of 6X loading dye
  • Well 42 to 49 : 5µL of RBS-BphR2+1µl of 6X loading dye
  • WEll 50 : 6µL DNA Ladder
  • Gel : 1%

Expect sizes :

  • FNR : 1096 bp
  • RBS-FNR : 1014 bp
  • RBS-BphR2 : 1469 bp

We obtain fragment at right size for FNR and RBS-FNR. The Gisbon assembly of 08/26/13 was good.