Team:Bielefeld-Germany/Labjournal/July

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===Milestones===
===Milestones===
*Poster presentation at the congress ‘[http://www.biotechnologie2020plus.de Next generation of biotechnological processes 2020+]’ in Berlin.
*Poster presentation at the congress ‘[http://www.biotechnologie2020plus.de Next generation of biotechnological processes 2020+]’ in Berlin.
-
<br><br><br><br>
+
*[[Team:Bielefeld-Germany/Partners|Sponsoring]] acquisition is nearly finished.
 +
*Problems with cloning delay the progress in the laboratory.
 +
*We have published our [http://ekvv.uni-bielefeld.de/blog/uniaktuell/entry/mit_bakterien_batterie_strom_erzeugen first press release] with a great response. The press release was picked up worldwide.
 +
<br><br>
-
===9.Week===
+
 
 +
===Week 9===
====Organization====
====Organization====
-
*We’ve presented us at the congress ‘Next generation of biotechnological processes 2020+’ in Berlin at 27. June 2013. There we have met an expert (Dr. Falk Harnisch) on the topic of MFC and we have decided to participate the German Synthetic Biology Day.
+
*We’ve presented us at the congress ‘[http://www.biotechnologie2020plus.de Next generation of biotechnological processes 2020+]’ in Berlin at June 27th, 2013. We met the expert (Dr. Falk Harnisch) on the topic of MFC and decided to participate in the [https://2013.igem.org/Team:Bielefeld-Germany/Human_Practice/Day_of_Synthetic_Biology 'Day of Synthetic Biology in Germany'].
====MFC====
====MFC====
-
 
+
*Started designing 3D models of MFCs which can be printed out by a 3D-printer
-
 
+
*Conducted experiments with ''saccharomyces cerevisiae'' and ''e. coli'' and recorded power curves for both
-
====Mediators====
+
*Ordered plastic parts for the new fuel cell model
-
 
+
====Cytochromes====
====Cytochromes====
-
*Design and order of new Primers
+
*Design and order of new primers
-
**The mtrCAB fragment has two illegal PstI restriction sites at x xbp and yy bp, so we had to design new primers to remove them. We replaced one base in each restriction site, without affecting the coding triplett, by respective primer overlaps . We ended up with three different fragments, which will be ligated back together via Gibson Assembly.
+
**The ''mtrCAB'' fragment has two illegal ''Pst''I restriction sites at 1793 bp and 2078 bp, so specific primers to remove them had to be designed. One base in each restriction site was replaced by respective primer overlaps without affecting the coding triplet. The three different fragments will be ligated back together and into the pSB1C3 shipping plasmid via Gibson Assembly.
-
**mtrCAB_Frag1_rev:
+
**''mtrCAB''_Frag1_rev (30 nt): GACCTGTTTTATCTGTTGCAGCGGCAGTAT
-
**mtrCAB_Frag2_fwd:     
+
**''mtrCAB''_Frag2_fwd (30 nt): ATACTGCCGCTGCAACAGATAAAACAGGTC    
-
**mtrCAB_Frag2_rev:  
+
**''mtrCAB''_Frag2_rev (30 nt): GGTGTGACGACTAATGCCATAATTGCAGAC 
-
**mtrCAB_Frag3_fwd:  
+
**''mtrCAB''_Frag3_fwd (30 nt): GTCTGCAATTATGGCATTAGTCGTCACACC 
-
====Biosafety====
+
====Nanowires====
 +
*Primer design for isolation of gene-cluster GSU 1776-1784 from ''Geobacter sulfurreducens'', containing overlaps for BioBrick Prefix and Suffix:
 +
**Forward GSU 1776-1784 (41):<br>GAATTCGCGGCCGCTTCTAGATGCTGAAACGTTTTCGTAAC
 +
**Reverse GSU 1776-1784 (44): <br>CTGCAGCGGCCGCTACTAGTATCATCCTACAGTGCCGGCAATTT
 +
<br>
 +
*Successful genome isolation from ''Geobacter sulfurreducens'' strain, using the GenEluteTM Bacterial Genomic DNA-Kit to prevent vigorous fragmentation of the DNA, which arises out of the standard genome isolation method with a ribolyse-step.
 +
*Successful PCR with forward and reverse primer GSU Promoter 1496-1505 and GSU 1496-1505 on the appropriate gene-cluster of ''Geobacter sulfurreducens'', using the PCR Master Mix, described in Table 3 (June) (nanowires), with adjusted template volume and the standard PCR program for amplification of ''Geobacter sulfurreducens'' gene cluster (Table 4, June).
 +
*GSU Promoter 1496-1505 and GSU 1496-1505 PCR products were isolated and purified by gel extraction.
 +
<br>
 +
[[File:iGEM_Bielefeld_2013_02.07.13_Wires.jpg|left|400px|thumb|'''Figure 1:''' Agarose gel from PCR on the gene-clusters GSU Promoter 1496-1505 (bands 2-5) and GSU 1496-1505 (bands 7-10) of ''Geobacter sulfurreducens'' strain. Ladder: GeneRuler™ 1 kb DNA Ladder from Thermo Scientific.]]
 +
<br><br>
-
 
+
===Week 10===
-
===10.Week===
+
====Organization====
====Organization====
-
*We can present new sponsors of iGEM-Team Bielefeld: Stockmeier, Baxter, Promega, BIO.NRW and Applichem will support our team.
+
*We can present new sponsors of iGEM-Team Bielefeld: Stockmeier, Baxter, Promega, BIO.NRW and AppliChem will support our team.
====MFC====
====MFC====
-
 
+
*Received plastic parts and built the first of our second generation fuel cells
====Mediators====
====Mediators====
*Glycerol dehydrogenase
*Glycerol dehydrogenase
-
**Further work on GldA Biobrick is needed: Plasmid [[Team:Bielefeld-Germany/Labjournal/Molecular#Restriction analysis|restriction analysis]] and [[Team:Bielefeld-Germany/Labjournal/Molecular#Colony PCR |colony PCR]] could not give sufficient results.  
+
**Further work on ''gldA'' BioBrick is needed: Plasmid [[Team:Bielefeld-Germany/Labjournal/Molecular#Restriction analysis|restriction analysis]] and [[Team:Bielefeld-Germany/Labjournal/Molecular#Colony PCR |colony PCR]] could not give sufficient results.  
-
**Successful PCR (standard Phusion PCR) on the <bbpart>BBa_J04450</bbpart> Biobrick plasmid using Forward Primer pSB1C3 and Reverse Primer pSB1C3 for later [[Team:Bielefeld-Germany/Labjournal/Molecular#Gibson assembly | Gibson Assembly]].
+
**Successful PCR (standard Phusion PCR) on the <bbpart>BBa_J04450</bbpart> BioBrick plasmid using forward primer pSB1C3 and reverse primer pSB1C3 for later [[Team:Bielefeld-Germany/Labjournal/Molecular#Gibson assembly | Gibson Assembly]].
-
**[[Team:Bielefeld-Germany/Labjournal/Molecular#Gibson assembly |Gibson Assembly]] with GldA PCR product and pSB1C3 PCR product.
+
**[[Team:Bielefeld-Germany/Labjournal/Molecular#Gibson assembly|Gibson Assembly]] with ''gldA'' PCR product and pSB1C3 PCR product.
-
**Screening of colonies from [[Team:Bielefeld-Germany/Labjournal/Molecular#Gibson assembly | Gibson Assembly]] with [[Team:Bielefeld-Germany/Labjournal/Molecular#Colony PCR | colony PCR]] and Plasmid [[Team:Bielefeld-Germany/Labjournal/Molecular#Restriction analysis| restriction analysis]] shows religated pSB1C3, as already seen while using [[Team:Bielefeld-Germany/Labjournal/Molecular#NEB Biobrick Assembly Kit | NEB Assembly Kit]].
+
**Screening of colonies from [[Team:Bielefeld-Germany/Labjournal/Molecular#Gibson assembly | Gibson Assembly]] with [[Team:Bielefeld-Germany/Labjournal/Molecular#Colony PCR | colony PCR]] and plasmid [[Team:Bielefeld-Germany/Labjournal/Molecular#Restriction analysis| restriction analysis]] shows re-ligated pSB1C3, as already seen while using [[Team:Bielefeld-Germany/Labjournal/Molecular#NEB BioBrick Assembly Kit | NEB Assembly Kit]].
-
====Cytochromes====
+
====Porines====
 +
*We will try to use [[Team:Bielefeld-Germany/Labjournal/Molecular#Gibson assembly | Gibson Assembly]] for cloning ''oprF'' into pSB1C3.
 +
*[[Team:Bielefeld-Germany/Labjournal/Molecular#Gibson assembly | Gibson Assembly]] with ''oprF'' PCR product and pSB1C3 PCR product. Screening of colonies from [[Team:Bielefeld-Germany/Labjournal/Molecular#Gibson assembly|Gibson Assembly]] with [[Team:Bielefeld-Germany/Labjournal/Molecular#Colony PCR | colony PCR]] and plasmid [[Team:Bielefeld-Germany/Labjournal/Molecular#Restriction analysis| restriction analysis]] shows re-ligated pSB1C3, as already seen while using [[Team:Bielefeld-Germany/Labjournal/Molecular#NEB Biobrick Assembly Kit | NEB Assembly Kit]].
-
====Biosafety====
+
====Nanowires====
 +
*PCR with forward and reverse primer GSU 1776-1784 on the appropriate gene-cluster of ''Geobacter sulfurreducens'' strain, using the PCR Master Mix, described in Table 3 (June) with adjusted template volume and the standard PCR program for amplification of ''Geobacter sulfurreducens'' gene cluster (Table 4, June) did not work as expected.
 +
*Bands of several sizes, but no band at the expected size of 9000 bp, the length of GSU 1776-1784. Because of the correct band for the control PCR on the gene cluster GSU Promoter 1496-1505 a problem with the PCR program can be eliminated.
 +
<br>
 +
[[File:iGEM_Bielefeld_2013_16.07.13_Wires.jpg|left|400px|thumb|'''Figure 2:''' Agarose gel from PCR on the gene-clusters GSU 1776-1784 (bands 2-5), the GSU Promoter 1496-1505 (band 7) and ''Geobacter sulfurreducens'' strain. Ladder: NEB 2-Log DNA Ladder (0.1-10.0 kb).]]
 +
<br><br>
-
====Porines====
 
-
*We will try to use [[Team:Bielefeld-Germany/Labjournal/Molecular#Gibson assembly | Gibson Assembly]] for cloning OprF into pSB1C3.
 
-
*[[Team:Bielefeld-Germany/Labjournal/Molecular#Gibson assembly | Gibson Assembly]] with OprF PCR product and pSB1C3 PCR product. Screening of colonies from Gibson Assembly]] with [[Team:Bielefeld-Germany/Labjournal/Molecular#Colony PCR | colony PCR]] and Plasmid [[Team:Bielefeld-Germany/Labjournal/Molecular#Restriction analysis| restriction analysis]] shows religated pSB1C3, as already seen while using [[Team:Bielefeld-Germany/Labjournal/Molecular#NEB Biobrick Assembly Kit | NEB Assembly Kit]].
 
 +
===Week 11===
-
===11.Week===
 
====Organization====
====Organization====
-
*We’ve presented us at the congress [http://www.bio.nrw.de/studentconvention BioNRW pHD Student Convention]in Düsseldorf at 13. July 2013 with a short presentation about iGEM and our project.
+
*We’ve presented us at the congress '[http://www.bio.nrw.de/studentconvention BioNRW pHD Student Convention]' in Düsseldorf at July 13th, 2013 with a short presentation about iGEM and our project.
*We proudly present our [http://ekvv.uni-bielefeld.de/blog/uniaktuell/entry/mit_bakterien_batterie_strom_erzeugen first press release.] It was amazing to see how often our press release was picked up.
*We proudly present our [http://ekvv.uni-bielefeld.de/blog/uniaktuell/entry/mit_bakterien_batterie_strom_erzeugen first press release.] It was amazing to see how often our press release was picked up.
====MFC====
====MFC====
-
 
+
*Recorded power output of ''e. coli'' in our second generation fuel cell
 +
*Manufactered different electrodes out of carbon tissue and tested them
====Mediators====
====Mediators====
*Glycerol dehydrogenase
*Glycerol dehydrogenase
-
**Repeating [[Team:Bielefeld-Germany/Labjournal/Molecular#Gibson assembly | Gibson Assembly]] shows every time a religated pSB1C3, a Gibson overlap of Prefix and Suffix with 20 bp seems to be to short, furthermore Prefix and Suffix have too many homologous regions.
+
**Repeating [[Team:Bielefeld-Germany/Labjournal/Molecular#Gibson assembly | Gibson Assembly]] shows every time a re-ligated pSB1C3, a Gibson overlap of Prefix and Suffix with 20 bp seems to be too short, furthermore Prefix and Suffix have too many homologous regions.
-
====Cytochromes====
+
====Porines====
 +
*Repeating [[Team:Bielefeld-Germany/Labjournal/Molecular#Gibson assembly | Gibson Assembly]] shows every time a re-ligated pSB1C3, a Gibson overlap of Prefix and Suffix with 20 bp seems to be too short, furthermore Prefix and Suffix have too many homologous regions.
-
====Biosafety====
+
====Nanowires====
 +
*Gibson Assembly with GSU 1491-1495, GSU 1496-1505 and GSU Promoter 1496-1505 PCR product as one fragment and the pSB1C3 PCR product, using the primer with Prefix and Suffix specific overlaps, as the second DNA fragment.
 +
*Screening of colonies from Gibson Assembly by plasmid restriction analysis shows fragments of 2000 bp, which corresponds to re-ligated pSB1C3.
 +
*PCR with forward and reverse primer GSU 1776-1784 on the appropriate gene-cluster of ''Geobacter sulfurreducens'' strain, using the PCR Master Mix, described in Table 3 (June) with adjusted template volume was repeated with the standard PCR program for amplification of ''Geobacter sulfurreducens'' gene cluster (Table 4, June) modified by a gradient of different annealing temperatures in a range of 45°C to 65°C.
 +
*No bands at the expected size of 9000 bp.
 +
<br><br>
-
====Porines====
 
-
*Repeating [[Team:Bielefeld-Germany/Labjournal/Molecular#Gibson assembly | Gibson Assembly]] shows every time a religated pSB1C3, a Gibson overlap of Prefix and Suffix with 20 bp seems to be to short, furthermore Prefix and Suffix have too many homologous regions.
 
-
===12.Week===
+
===Week 12===
 +
 
====Organization====
====Organization====
*Dr. Falk Harnisch will have a presentation at CeBiTec colloquium as an expert for our team.
*Dr. Falk Harnisch will have a presentation at CeBiTec colloquium as an expert for our team.
-
*Preparing experiments for the ‘[https://2013.igem.org/Team:Bielefeld-Germany/Human_Practice/Day_of_Synthetic_Biology Day of Synthetic Biology]’. Our ideas are to have different experiments like DNA isolation from fruit and vegetables, pipetting of bright colors, chromatography with markers, a potato battery or microscopy.
+
*Preparing experiments for the ‘[https://2013.igem.org/Team:Bielefeld-Germany/Human_Practice/Day_of_Synthetic_Biology Day of Synthetic Biology]’. Our ideas are experiments like DNA isolation from fruit and vegetables, pipetting of bright colors, chromatography with markers, a potato battery and microscopy.
*The TV station [http://www1.wdr.de/mediathek/video/sendungen/lokalzeit/lokalzeit-owl WDR] would like to contribute with us on our topic.
*The TV station [http://www1.wdr.de/mediathek/video/sendungen/lokalzeit/lokalzeit-owl WDR] would like to contribute with us on our topic.
====MFC====
====MFC====
-
 
+
*Visited the local hackerspace where we learned the basics of using a 3D printer and spent the night trying to make it work with our computers.
 +
*Continued constructing and testing different electrode designs.
====Mediators====
====Mediators====
*Glycerol dehydrogenase
*Glycerol dehydrogenase
-
**New Primerdesign for pSB1C3 with longer overlaps individually for each part in order to stop the problem of religated pSB1C3:
+
**New primer design for pSB1C3 with longer overlaps individually for each part in order to stop the problem of re-ligated pSB1C3:
-
**Forward Primer pSB1C3 GldA (43 bp): TCCTGCAAGAGTGGGAATAATACTAGTAGCGGCCGCTGCAGTC
+
**Forward primer pSB1C3 ''gldA'' (43 bp): TCCTGCAAGAGTGGGAATAATACTAGTAGCGGCCGCTGCAGTC
-
**Reverse Primer pSB1C3 GldA (43 bp): GATTGAATAATGCGGTCCATCTAGAAGCGGCCGCGAATTCCAG
+
**Reverse primer pSB1C3 ''gldA'' (43 bp): GATTGAATAATGCGGTCCATCTAGAAGCGGCCGCGAATTCCAG
Line 135: Line 147:
-
*Amplification of Fragment 1
+
*Amplification of Fragment1 with [https://2013.igem.org/Team:Bielefeld-Germany/Labjournal/Molecular#Used_enzymes Phusion polymerase]
-
**Size: 1800 bp
+
**Size: 1833 bp
-
**Program: [[Team:Bielefeld-Germany/Labjournal/ProtocolsPrograms#cyt_frag1|PhusionPCR]]
+
**Gradient: 54°C - 71°C over 8 steps
**Gradient: 54°C - 71°C over 8 steps
-
**Primer: mtrC_fwd & mtr_Frag1_rev
+
**Primer: 'mtrC'_fwd & mtr_Frag1_rev
-
**Template: S. oneidensis PCR Template from genomic DNA
+
**Template: ''S. oneidensis'' PCR Template from genomic DNA
**Notes: Annealing temperature has no significant impact on the PCR
**Notes: Annealing temperature has no significant impact on the PCR
-
*Amplification of Fragment 2
+
*Amplification of Fragment2 with  [https://2013.igem.org/Team:Bielefeld-Germany/Labjournal/Molecular#Used_enzymes Phusion polymerase]
-
**Size: 330 bp
+
**Size: 321 bp
-
**Program: [[Team:Bielefeld-Germany/Labjournal/ProtocolsPrograms#cyt_frag2|PhusionPCR]]
+
**Primer: mtr_Frag2_fwd & mtr_Frag2_rev
**Primer: mtr_Frag2_fwd & mtr_Frag2_rev
-
**Template: S. oneidensis PCR Template from genomic DNA
+
**Template: ''S. oneidensis'' PCR Template from genomic DNA
-
**Notes:  
+
**Notes: Annealing temperature has no significant impact on the PCR
-
*Amplification of Fragment 3
+
*Amplification of Fragment3 with [https://2013.igem.org/Team:Bielefeld-Germany/Labjournal/Molecular#Used_enzymes Phusion polymerase]
-
**Size: 3000 bp
+
**Size: 3057 bp
-
**Program: [[Team:Bielefeld-Germany/Labjournal/ProtocolsPrograms#cyt_frag3|PhusionPCR]]
+
**Gradient: 54°C - 71°C over 8 steps
**Gradient: 54°C - 71°C over 8 steps
**Primer: mtr_Frag3_fwd & mtrB_rev
**Primer: mtr_Frag3_fwd & mtrB_rev
-
**Template: S. oneidensis PCR Template from genomic DNA
+
**Template: ''S. oneidensis'' PCR Template from genomic DNA
-
**Notes: Annealing temperature has no significant impact on the PCR
+
**Notes:  
-
*Amplification of ccmAH cluster
+
*Amplification of ''ccmAH'' cluster
**Size:6311 bp
**Size:6311 bp
**Program: [[Team:Bielefeld-Germany/Labjournal/ProtocolsPrograms#cyt_ccmAH|PhusionPCR]]
**Program: [[Team:Bielefeld-Germany/Labjournal/ProtocolsPrograms#cyt_ccmAH|PhusionPCR]]
**Gradient: 51.5°C - 68°C over 8 steps
**Gradient: 51.5°C - 68°C over 8 steps
**Primer: ccmAH_fwd & ccmAH_rev
**Primer: ccmAH_fwd & ccmAH_rev
-
**Template: E. coli PCR Template from genomic DNA
+
**Template: ''E. coli'' PCR Template from genomic DNA
**Notes: A high annealing temperature of 68°C or more increases yield as well as reduces unspecific bands and is therefore recommended.
**Notes: A high annealing temperature of 68°C or more increases yield as well as reduces unspecific bands and is therefore recommended.
-
*Gelextraction and cleanup of Fragment 1, 2, 3 and ccmAH
+
[[Image:Bielefeld-Germany2013_ccm_gradient.jpg|300px|thumb|left|<p align="justify"> '''Figure 3: Results of a PAGE of an amplification of ''ccmAH''; Expected Size: 6.3kb; Gradient:  51.5-68°C; Ladder:Thermo Scientific GeneRuler™ 1 kb DNA Ladder.</p>]]
-
**Gelextraction and clean up with the AnalytikJena GelExtraction-Kit
+
 
 +
 
 +
*[https://2013.igem.org/Team:Bielefeld-Germany/Labjournal/ProtocolsPrograms#Used_Kits Gel extraction and cleanup] of Fragment 1, 2, 3 and ''ccmAH''
**Elution buffer was preheated to 50°C
**Elution buffer was preheated to 50°C
**We eluted each column twice, with 20 ul each and combined it afterwards
**We eluted each column twice, with 20 ul each and combined it afterwards
-
**Measurement of nucleid acid concentration via NanoDrop
+
**Measurement of nucleic acid concentration via NanoDrop
-
***Fragment1: 4-2607-304: 10.5 ng/ul</p>
+
***Fragment1: 4-2607-304: 10.5 ng/ul
-
***Fragment2: 4-2707-003: 44.6 ng/ul</p>
+
***Fragment2: 4-2707-003: 44.6 ng/ul
-
***Fragment2: 4-2707-004: 13.5 ng/ul</p>
+
***Fragment2: 4-2707-004: 13.5 ng/ul
-
***Fragment3: 4-2607-301: 11.1 ng/ul</p>
+
***Fragment3: 4-2607-301: 11.1 ng/ul
-
***Fragment3: 4-2607-302: 8.9 ng/ul</p>
+
***Fragment3: 4-2607-302: 8.9 ng/ul
-
***Fragment3: 4-2607-303: 9.2 ng/ul</p>
+
***Fragment3: 4-2607-303: 9.2 ng/ul
-
***ccmAH: 4-2807-302: 11.0 ng/ul</p>
+
***''ccmAH'': 4-2807-302: 11.0 ng/ul
-
***ccmAH: 4-2807-303: 11.5 ng/ul</p>
+
***''ccmAH'': 4-2807-303: 11.5 ng/ul
-
====Cytochromes====
+
====Porines====
 +
*New primer design for pSB1C3 with longer overlaps individually for OprF part in order to stop the problem of re-ligated pSB1C3:
 +
*Forward primer pSB1C3 ''oprF'' (43 bp): TTGAAGCCCAAGCTAAGTAATACTAGTAGCGGCCGCTGCAGTC
 +
*Reverse primer pSB1C3 ''oprF'' (43 bp): AAGGTGTTTTTCAGTTTCATCTAGAAGCGGCCGCGAATTCCAG
 +
====Nanowires====
-
====Biosafety====
+
*Multiple Gibson Assembly retries with different molar ratios of the two fragments results every time in re-ligated pSB1C3 plasmids, so that the used Gibson overlap of Prefix and Suffix is not useable.
 +
*Design of new primers for pSB1C3 amplification with longer sequence-specific overlaps for every part:
 +
**Forward pSB1C3 GSU 1491-1505 / GSU 1496-1505 / GSU Promoter 1496-1505 (43 bp): <br>GGGACGAGGTTCGTTTATGATACTAGTAGCGGCCGCTGCAGTC
 +
**Reverse pSB1C3 GSU 1496-1505 (43 bp):<br> GTATGGGGGTAATTGGCCAACTCTAGAAGCGGCCGCGAATTCC
 +
**Forward pSB1C3 GSU 1491-1495 (43 bp):<br> TTGGCATGGATGAGGAGTGATACTAGTAGCGGCCGCTGCAGTC
 +
**Reverse pSB1C3 GSU 1491-1495 / GSU 1491-1505 (43 bp):<br> CCCAGTCTGCTAGCCTGCATCTAGAAGCGGCCGCGAATTCCAG
 +
**Reverse pSB1C3 GSU Promoter 1496-1505 (43 bp): <br>ACTCGGTGACGGATCCTATCCTCTAGAAGCGGCCGCGAATTCC
 +
<br><br>
-
====Porines====
 
-
*New Primerdesign for pSB1C3 with longer overlaps individually for OprF part in order to stop the problem of religated pSB1C3:
 
-
*Forward Primer pSB1C3 OprF (43 bp): TTGAAGCCCAAGCTAAGTAATACTAGTAGCGGCCGCTGCAGTC
 
-
*Reverse Primer pSB1C3 OprF (43 bp): AAGGTGTTTTTCAGTTTCATCTAGAAGCGGCCGCGAATTCCAG
 
-
 
+
===Week 13===
-
<br><br><br><br>
+
-
<br><br><br><br>
+
-
 
+
-
 
+
-
===13.Week===
+
====Organization====
====Organization====
*Spontaneous visit of [http://www.radiobielefeld.de Radio Bielefeld] in our laboratory. In addition to a radio interview a [http://www.radiobielefeld.de/programm/bei-uns-im-programm/studenten-entwickeln-biobatterie.html short video clip] was filmed.
*Spontaneous visit of [http://www.radiobielefeld.de Radio Bielefeld] in our laboratory. In addition to a radio interview a [http://www.radiobielefeld.de/programm/bei-uns-im-programm/studenten-entwickeln-biobatterie.html short video clip] was filmed.
-
 
-
 
-
====MFC====
 
====Mediators====
====Mediators====
-
 
+
* Phenazine
-
 
+
<p align="justify">
-
====Cytochromes====
+
Almost ten PCRs were run up to this time. Unfortunately, none of them was successful. We show only two gel pictures out of many, where two different gradients were taken.
 +
We have tried to add betaine as a stabilizing agent, work with [http://www.millipore.com/publications.nsf/a73664f9f981af8c852569b9005b4eee/31140b3dbc2b4146852579d8005e9c72/$FILE/PR3366EN00.pdf KOD Hot Start polymerase] according to the manual. We tried different extention times and annealing in different temperatures.
 +
<br>
 +
The fragment [https://2013.igem.org/Team:Bielefeld-Germany/Project/Phenazine ''PhzABCDEFGH''] contains 8 illegal restriction sites and is 8505 bp long.
 +
After trying all strategies, we decided to abandon this sub-project and start with another endogenous mediator, riboflavin (see [https://2013.igem.org/Team:Bielefeld-Germany/Labjournal/August Labjournal August])</p>
 +
<ol>
 +
<li>Recipe PCR
 +
<ul><li>2x KOD Xtreme™ PCR Buffer: 25 µL</li>
 +
<li>dNTPs: 1.0 µL</li>
 +
<li>Primer1: 1.0 µL</li>
 +
<li>Primer2: 1.0 µL</li>
 +
<li>Template DNA: 1.5 µL</li>
 +
<li>DMSO: 1.5 µL</li>
 +
<li>Betaine: 12.5 µL</li>
 +
<li>KOD Hot Start Polymerase: 0.5 µL</li>
 +
<li>Dest. H2O: 6 µL</li>
 +
<li>Total volume: 50 µL</li>
 +
</ul></li>
 +
<li>Protocol PCR Two-step Cycling</li>
 +
<ul><li>Polymerase Activation 94°C for 2 min</li>
 +
<li>Denaturation 98°C for 10 s</li>
 +
<li>Annealing gradient 50.8°C-70.2°C</li>
 +
<li>Extension 72°C for 270 s/320 s</li>
 +
</ul></li></ol>
 +
<br>
 +
[[File:IGEM Bielefeld 2013 PCR gradient Phenzine.jpg|300px|thumb|left| '''PCR for ''PhzABCDEFGH''-gene cluster''', gradient with KOD-Polymerase, 270 s extension]]
 +
[[File:IGEM Bielefeld 2013 PCR gradient Phenzine2.jpg|300px|thumb|right| '''PCR for ''PhzABCDEFGH''-gene cluster''', gradient with KOD-Polymerase, 320 s extension]]
 +
<br><br><br><br><br><br><br><br><br><br><br><br><p align="justify">
 +
As is clear from the gels, we were not able to amplify the fragment and have closed this sub-project.</p>
Line 217: Line 255:
*Recipe:
*Recipe:
-
**PhusionBuffer: 5,5µL
+
**PhusionBuffer: 5.5 µL
-
**dNTPs: 1µL
+
**dNTPs: 1 µL
-
**Primer1: 1µL
+
**Primer1: 1 µL
-
**Primer2: 1µL
+
**Primer2: 1 µL
-
**Template: 1,5 µL
+
**Template: 1.5 µL
-
**DMSO: 0,5 µL
+
**DMSO: 0.5 µL
-
**Phusion: 0,5 µL
+
**Phusion: 0.5 µL
-
**Dest. H2O: 39 µL
+
**Dest. H<sub>2</sub>O: 39 µL
-
*1.AraC:
+
*1.''araC'':
**Primer: araC_d1+ araC_d2
**Primer: araC_d1+ araC_d2
**Annealing: 62°C
**Annealing: 62°C
-
**Extension: 1min
+
**Extension: 1 min
-
**Template: E.coli Genome
+
**Template: ''E.coli'' Genome
**Size: 600 bp
**Size: 600 bp
<br>
<br>
-
*2.Deletion of araC:
+
*2.Deletion of ''araC'':
**Primer: araC_d3+ araC_d4
**Primer: araC_d3+ araC_d4
**Annealing= 62°C
**Annealing= 62°C
-
**Extension: 1min
+
**Extension: 1 min
-
**Template: E.coli Genome
+
**Template: ''E.coli'' Genome
**Size: 600 bp
**Size: 600 bp
-
*3.Amplification of araC into our Biosafety system:
+
*3.Amplification of ''araC'' into our Biosafety system:
**Primer: araC_fwd+ araC rev
**Primer: araC_fwd+ araC rev
**Annealing= 62°C
**Annealing= 62°C
-
**Extension: 1min
+
**Extension: 1 min
**Template: BBa_I13458
**Template: BBa_I13458
**Size: 900 bp
**Size: 900 bp
Line 263: Line 301:
**Annealing: 62°C
**Annealing: 62°C
**Extension: 1 min
**Extension: 1 min
-
**Template: E.coli Genome
+
**Template: ''E.coli'' Genome
-
**Size: 1kb
+
**Size: 1 kb
Line 270: Line 308:
**Primer: pSB1C3_plac_alr+ pSB1C3_alr_rev
**Primer: pSB1C3_plac_alr+ pSB1C3_alr_rev
**Annealing: 62°C
**Annealing: 62°C
-
**Extension: 1min
+
**Extension: 1 min
-
**Template: E.coli Genome
+
**Template: ''E.coli'' Genome
-
**Size: 1kb
+
**Size: 1 kb
Line 280: Line 318:
**Extension: 1.30 min
**Extension: 1.30 min
**Template: pSB1C3
**Template: pSB1C3
-
**Size: 2kb
+
**Size: 2 kb
Line 288: Line 326:
**Extension: 1.30min
**Extension: 1.30min
**Template: pSB1C3
**Template: pSB1C3
-
**Size: 2kb
+
**Size: 2 kb
-
*Analysis by agarosegel
+
*Analysis by agarose gel
**Result:failed
**Result:failed
<br>
<br>
Line 297: Line 335:
*New PCR:
*New PCR:
**Program: 06 phy_cyt mit 62°C Annealing
**Program: 06 phy_cyt mit 62°C Annealing
-
**10µL 5xHF-Buffer
+
**10 µL 5xHF-Buffer
-
**4µL dNTPs
+
**4 µL dNTPs
-
**0,5µL Primer1
+
**0.5 µL Primer1
-
**0,5µL Primer2
+
**0.5 µL Primer2
-
**1µL Template
+
**1 µL Template
-
**1,5µL DMSO
+
**1.5 µL DMSO
-
**1µL Enzyme
+
**1 µL Enzyme
-
**31,5µL dest. H2O
+
**31.5 µL dest. H<sub>2</sub>O
<br>
<br>
-
*Analysis by agarosegel:
+
*Analysis by agarose gel:
-
[[File:IGEM Bielefeld 2013 Biosafety S.112 1-4.png|200px|thumb|left|Gelanalysis of PCR 1-4.]][[File:IGEM Bielefeld 2013 Biosafety S.112 5-8.jpg|200px|thumb|center|Gelanalysis of PCR 5-8.]]
+
[[File:IGEM Bielefeld 2013 Biosafety S.112 1-4.png|200px|thumb|left|Gelanalysis of PCR 1-4.]][[File:IGEM Bielefeld 2013 Biosafety S.112 5-8.jpg|200px|thumb|center|Gel analysis of PCR 5-8.]]
*PCR-Purification:
*PCR-Purification:
-
**BS1a (9-38-451) 113,6ng/µL<br>
+
**BS1a (9-38-451) 113.6 ng/µL<br>
-
**BS1b (9-38-452) 75,1 ng/µL<br>
+
**BS1b (9-38-452) 75.1 ng/µL<br>
-
**BS2a (9-38-453) 85,5 ng/µL<br>
+
**BS2a (9-38-453) 85.5 ng/µL<br>
-
**BS3a (9-38-454) 107,6 ng/µL<br>
+
**BS3a (9-38-454) 107.6 ng/µL<br>
-
**BS4a (9-38-455) 14,4 ng/µL<br>
+
**BS4a (9-38-455) 14.4 ng/µL<br>
-
**BS5a (9-38-456) 44,5 ng/µL<br>
+
**BS5a (9-38-456) 44.5 ng/µL<br>
-
**BS5b (9-38-457) 49,0 ng/µL<br>
+
**BS5b (9-38-457) 49.0 ng/µL<br>
-
**BS6a (9-38-458) 63,6 ng/µL<br>
+
**BS6a (9-38-458) 63.6 ng/µL<br>
-
**BS7a (9-38-459) 6,9 ng/µL<br>
+
**BS7a (9-38-459) 6.9 ng/µL<br>
-
**BS8a (9-38-460) 8,6 ng/µL<br>
+
**BS8a (9-38-460) 8.6 ng/µL<br>
 +
<br>
 +
*Successful PCR on the BBa_J04450 BioBrick plasmid using part specific forward and reverse primer (Week 12) for later Gibson Assembly. Isolation of the pSB1C3 PCR product by agarose gel electrophoresis and gel extraction.
 +
*Gibson Assembly, using the different new pSB1C3 PCR products and the according gene-cluster PCR products.
Line 329: Line 370:
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Latest revision as of 23:58, 28 October 2013



July


Milestones

  • Poster presentation at the congress ‘[http://www.biotechnologie2020plus.de Next generation of biotechnological processes 2020+]’ in Berlin.
  • Sponsoring acquisition is nearly finished.
  • Problems with cloning delay the progress in the laboratory.
  • We have published our [http://ekvv.uni-bielefeld.de/blog/uniaktuell/entry/mit_bakterien_batterie_strom_erzeugen first press release] with a great response. The press release was picked up worldwide.




Week 9

Organization

  • We’ve presented us at the congress ‘[http://www.biotechnologie2020plus.de Next generation of biotechnological processes 2020+]’ in Berlin at June 27th, 2013. We met the expert (Dr. Falk Harnisch) on the topic of MFC and decided to participate in the 'Day of Synthetic Biology in Germany'.


MFC

  • Started designing 3D models of MFCs which can be printed out by a 3D-printer
  • Conducted experiments with saccharomyces cerevisiae and e. coli and recorded power curves for both
  • Ordered plastic parts for the new fuel cell model

Cytochromes

  • Design and order of new primers
    • The mtrCAB fragment has two illegal PstI restriction sites at 1793 bp and 2078 bp, so specific primers to remove them had to be designed. One base in each restriction site was replaced by respective primer overlaps without affecting the coding triplet. The three different fragments will be ligated back together and into the pSB1C3 shipping plasmid via Gibson Assembly.
    • mtrCAB_Frag1_rev (30 nt): GACCTGTTTTATCTGTTGCAGCGGCAGTAT
    • mtrCAB_Frag2_fwd (30 nt): ATACTGCCGCTGCAACAGATAAAACAGGTC
    • mtrCAB_Frag2_rev (30 nt): GGTGTGACGACTAATGCCATAATTGCAGAC
    • mtrCAB_Frag3_fwd (30 nt): GTCTGCAATTATGGCATTAGTCGTCACACC


Nanowires

  • Primer design for isolation of gene-cluster GSU 1776-1784 from Geobacter sulfurreducens, containing overlaps for BioBrick Prefix and Suffix:
    • Forward GSU 1776-1784 (41):
      GAATTCGCGGCCGCTTCTAGATGCTGAAACGTTTTCGTAAC
    • Reverse GSU 1776-1784 (44):
      CTGCAGCGGCCGCTACTAGTATCATCCTACAGTGCCGGCAATTT


  • Successful genome isolation from Geobacter sulfurreducens strain, using the GenEluteTM Bacterial Genomic DNA-Kit to prevent vigorous fragmentation of the DNA, which arises out of the standard genome isolation method with a ribolyse-step.
  • Successful PCR with forward and reverse primer GSU Promoter 1496-1505 and GSU 1496-1505 on the appropriate gene-cluster of Geobacter sulfurreducens, using the PCR Master Mix, described in Table 3 (June) (nanowires), with adjusted template volume and the standard PCR program for amplification of Geobacter sulfurreducens gene cluster (Table 4, June).
  • GSU Promoter 1496-1505 and GSU 1496-1505 PCR products were isolated and purified by gel extraction.


Figure 1: Agarose gel from PCR on the gene-clusters GSU Promoter 1496-1505 (bands 2-5) and GSU 1496-1505 (bands 7-10) of Geobacter sulfurreducens strain. Ladder: GeneRuler™ 1 kb DNA Ladder from Thermo Scientific.




Week 10

Organization

  • We can present new sponsors of iGEM-Team Bielefeld: Stockmeier, Baxter, Promega, BIO.NRW and AppliChem will support our team.


MFC

  • Received plastic parts and built the first of our second generation fuel cells

Mediators


Porines


Nanowires

  • PCR with forward and reverse primer GSU 1776-1784 on the appropriate gene-cluster of Geobacter sulfurreducens strain, using the PCR Master Mix, described in Table 3 (June) with adjusted template volume and the standard PCR program for amplification of Geobacter sulfurreducens gene cluster (Table 4, June) did not work as expected.
  • Bands of several sizes, but no band at the expected size of 9000 bp, the length of GSU 1776-1784. Because of the correct band for the control PCR on the gene cluster GSU Promoter 1496-1505 a problem with the PCR program can be eliminated.


Figure 2: Agarose gel from PCR on the gene-clusters GSU 1776-1784 (bands 2-5), the GSU Promoter 1496-1505 (band 7) and Geobacter sulfurreducens strain. Ladder: NEB 2-Log DNA Ladder (0.1-10.0 kb).




Week 11

Organization

  • We’ve presented us at the congress '[http://www.bio.nrw.de/studentconvention BioNRW pHD Student Convention]' in Düsseldorf at July 13th, 2013 with a short presentation about iGEM and our project.
  • We proudly present our [http://ekvv.uni-bielefeld.de/blog/uniaktuell/entry/mit_bakterien_batterie_strom_erzeugen first press release.] It was amazing to see how often our press release was picked up.


MFC

  • Recorded power output of e. coli in our second generation fuel cell
  • Manufactered different electrodes out of carbon tissue and tested them

Mediators

  • Glycerol dehydrogenase
    • Repeating Gibson Assembly shows every time a re-ligated pSB1C3, a Gibson overlap of Prefix and Suffix with 20 bp seems to be too short, furthermore Prefix and Suffix have too many homologous regions.


Porines

  • Repeating Gibson Assembly shows every time a re-ligated pSB1C3, a Gibson overlap of Prefix and Suffix with 20 bp seems to be too short, furthermore Prefix and Suffix have too many homologous regions.


Nanowires

  • Gibson Assembly with GSU 1491-1495, GSU 1496-1505 and GSU Promoter 1496-1505 PCR product as one fragment and the pSB1C3 PCR product, using the primer with Prefix and Suffix specific overlaps, as the second DNA fragment.
  • Screening of colonies from Gibson Assembly by plasmid restriction analysis shows fragments of 2000 bp, which corresponds to re-ligated pSB1C3.
  • PCR with forward and reverse primer GSU 1776-1784 on the appropriate gene-cluster of Geobacter sulfurreducens strain, using the PCR Master Mix, described in Table 3 (June) with adjusted template volume was repeated with the standard PCR program for amplification of Geobacter sulfurreducens gene cluster (Table 4, June) modified by a gradient of different annealing temperatures in a range of 45°C to 65°C.
  • No bands at the expected size of 9000 bp.




Week 12

Organization

  • Dr. Falk Harnisch will have a presentation at CeBiTec colloquium as an expert for our team.
  • Preparing experiments for the ‘Day of Synthetic Biology’. Our ideas are experiments like DNA isolation from fruit and vegetables, pipetting of bright colors, chromatography with markers, a potato battery and microscopy.
  • The TV station [http://www1.wdr.de/mediathek/video/sendungen/lokalzeit/lokalzeit-owl WDR] would like to contribute with us on our topic.


MFC

  • Visited the local hackerspace where we learned the basics of using a 3D printer and spent the night trying to make it work with our computers.
  • Continued constructing and testing different electrode designs.

Mediators

  • Glycerol dehydrogenase
    • New primer design for pSB1C3 with longer overlaps individually for each part in order to stop the problem of re-ligated pSB1C3:
    • Forward primer pSB1C3 gldA (43 bp): TCCTGCAAGAGTGGGAATAATACTAGTAGCGGCCGCTGCAGTC
    • Reverse primer pSB1C3 gldA (43 bp): GATTGAATAATGCGGTCCATCTAGAAGCGGCCGCGAATTCCAG


Cytochromes

  • Amplification of Fragment1 with Phusion polymerase
    • Size: 1833 bp
    • Gradient: 54°C - 71°C over 8 steps
    • Primer: 'mtrC'_fwd & mtr_Frag1_rev
    • Template: S. oneidensis PCR Template from genomic DNA
    • Notes: Annealing temperature has no significant impact on the PCR
  • Amplification of Fragment2 with Phusion polymerase
    • Size: 321 bp
    • Primer: mtr_Frag2_fwd & mtr_Frag2_rev
    • Template: S. oneidensis PCR Template from genomic DNA
    • Notes: Annealing temperature has no significant impact on the PCR
  • Amplification of Fragment3 with Phusion polymerase
    • Size: 3057 bp
    • Gradient: 54°C - 71°C over 8 steps
    • Primer: mtr_Frag3_fwd & mtrB_rev
    • Template: S. oneidensis PCR Template from genomic DNA
    • Notes:
  • Amplification of ccmAH cluster
    • Size:6311 bp
    • Program: PhusionPCR
    • Gradient: 51.5°C - 68°C over 8 steps
    • Primer: ccmAH_fwd & ccmAH_rev
    • Template: E. coli PCR Template from genomic DNA
    • Notes: A high annealing temperature of 68°C or more increases yield as well as reduces unspecific bands and is therefore recommended.

Figure 3: Results of a PAGE of an amplification of ccmAH; Expected Size: 6.3kb; Gradient: 51.5-68°C; Ladder:Thermo Scientific GeneRuler™ 1 kb DNA Ladder.


  • Gel extraction and cleanup of Fragment 1, 2, 3 and ccmAH
    • Elution buffer was preheated to 50°C
    • We eluted each column twice, with 20 ul each and combined it afterwards
    • Measurement of nucleic acid concentration via NanoDrop
      • Fragment1: 4-2607-304: 10.5 ng/ul
      • Fragment2: 4-2707-003: 44.6 ng/ul
      • Fragment2: 4-2707-004: 13.5 ng/ul
      • Fragment3: 4-2607-301: 11.1 ng/ul
      • Fragment3: 4-2607-302: 8.9 ng/ul
      • Fragment3: 4-2607-303: 9.2 ng/ul
      • ccmAH: 4-2807-302: 11.0 ng/ul
      • ccmAH: 4-2807-303: 11.5 ng/ul


Porines

  • New primer design for pSB1C3 with longer overlaps individually for OprF part in order to stop the problem of re-ligated pSB1C3:
  • Forward primer pSB1C3 oprF (43 bp): TTGAAGCCCAAGCTAAGTAATACTAGTAGCGGCCGCTGCAGTC
  • Reverse primer pSB1C3 oprF (43 bp): AAGGTGTTTTTCAGTTTCATCTAGAAGCGGCCGCGAATTCCAG

Nanowires

  • Multiple Gibson Assembly retries with different molar ratios of the two fragments results every time in re-ligated pSB1C3 plasmids, so that the used Gibson overlap of Prefix and Suffix is not useable.
  • Design of new primers for pSB1C3 amplification with longer sequence-specific overlaps for every part:
    • Forward pSB1C3 GSU 1491-1505 / GSU 1496-1505 / GSU Promoter 1496-1505 (43 bp):
      GGGACGAGGTTCGTTTATGATACTAGTAGCGGCCGCTGCAGTC
    • Reverse pSB1C3 GSU 1496-1505 (43 bp):
      GTATGGGGGTAATTGGCCAACTCTAGAAGCGGCCGCGAATTCC
    • Forward pSB1C3 GSU 1491-1495 (43 bp):
      TTGGCATGGATGAGGAGTGATACTAGTAGCGGCCGCTGCAGTC
    • Reverse pSB1C3 GSU 1491-1495 / GSU 1491-1505 (43 bp):
      CCCAGTCTGCTAGCCTGCATCTAGAAGCGGCCGCGAATTCCAG
    • Reverse pSB1C3 GSU Promoter 1496-1505 (43 bp):
      ACTCGGTGACGGATCCTATCCTCTAGAAGCGGCCGCGAATTCC




Week 13

Organization

  • Spontaneous visit of [http://www.radiobielefeld.de Radio Bielefeld] in our laboratory. In addition to a radio interview a [http://www.radiobielefeld.de/programm/bei-uns-im-programm/studenten-entwickeln-biobatterie.html short video clip] was filmed.


Mediators

  • Phenazine

Almost ten PCRs were run up to this time. Unfortunately, none of them was successful. We show only two gel pictures out of many, where two different gradients were taken. We have tried to add betaine as a stabilizing agent, work with [http://www.millipore.com/publications.nsf/a73664f9f981af8c852569b9005b4eee/31140b3dbc2b4146852579d8005e9c72/$FILE/PR3366EN00.pdf KOD Hot Start polymerase] according to the manual. We tried different extention times and annealing in different temperatures.
The fragment PhzABCDEFGH contains 8 illegal restriction sites and is 8505 bp long. After trying all strategies, we decided to abandon this sub-project and start with another endogenous mediator, riboflavin (see Labjournal August)

  1. Recipe PCR
    • 2x KOD Xtreme™ PCR Buffer: 25 µL
    • dNTPs: 1.0 µL
    • Primer1: 1.0 µL
    • Primer2: 1.0 µL
    • Template DNA: 1.5 µL
    • DMSO: 1.5 µL
    • Betaine: 12.5 µL
    • KOD Hot Start Polymerase: 0.5 µL
    • Dest. H2O: 6 µL
    • Total volume: 50 µL
  2. Protocol PCR Two-step Cycling
    • Polymerase Activation 94°C for 2 min
    • Denaturation 98°C for 10 s
    • Annealing gradient 50.8°C-70.2°C
    • Extension 72°C for 270 s/320 s


PCR for PhzABCDEFGH-gene cluster, gradient with KOD-Polymerase, 270 s extension
PCR for PhzABCDEFGH-gene cluster, gradient with KOD-Polymerase, 320 s extension












As is clear from the gels, we were not able to amplify the fragment and have closed this sub-project.


Biosafety

  • Amplification of different fragments:
  • Recipe:
    • PhusionBuffer: 5.5 µL
    • dNTPs: 1 µL
    • Primer1: 1 µL
    • Primer2: 1 µL
    • Template: 1.5 µL
    • DMSO: 0.5 µL
    • Phusion: 0.5 µL
    • Dest. H2O: 39 µL


  • 1.araC:
    • Primer: araC_d1+ araC_d2
    • Annealing: 62°C
    • Extension: 1 min
    • Template: E.coli Genome
    • Size: 600 bp


  • 2.Deletion of araC:
    • Primer: araC_d3+ araC_d4
    • Annealing= 62°C
    • Extension: 1 min
    • Template: E.coli Genome
    • Size: 600 bp


  • 3.Amplification of araC into our Biosafety system:
    • Primer: araC_fwd+ araC rev
    • Annealing= 62°C
    • Extension: 1 min
    • Template: BBa_I13458
    • Size: 900 bp


  • 4.Preparation of pSB1C3:
    • Primer: pRha_rev+ pSB1C3_rha_suf
    • Annealing: 62°C
    • Extension: 1.30 min
    • Template: BBa_I13541
    • Size: 3 kb


  • 5.Preparation of pSB1C3:
    • Primer: pSB1C3_alr_fwd+ pSB1C3_alr_rev
    • Annealing: 62°C
    • Extension: 1 min
    • Template: E.coli Genome
    • Size: 1 kb


  • 6.Preparation of pSB1C3:
    • Primer: pSB1C3_plac_alr+ pSB1C3_alr_rev
    • Annealing: 62°C
    • Extension: 1 min
    • Template: E.coli Genome
    • Size: 1 kb


  • 7.Preparation of pSB1C3:
    • Primer: pSB1C3_alr_pre+ pSB1C3_alr_suf
    • Annealing: 62°C
    • Extension: 1.30 min
    • Template: pSB1C3
    • Size: 2 kb


  • 8.Preparation of pSB1C3:
    • Primer: pSB1C3_plac_pre+ pSB1C3_alr_suf
    • Annealing: 62°C
    • Extension: 1.30min
    • Template: pSB1C3
    • Size: 2 kb


  • Analysis by agarose gel
    • Result:failed


  • New PCR:
    • Program: 06 phy_cyt mit 62°C Annealing
    • 10 µL 5xHF-Buffer
    • 4 µL dNTPs
    • 0.5 µL Primer1
    • 0.5 µL Primer2
    • 1 µL Template
    • 1.5 µL DMSO
    • 1 µL Enzyme
    • 31.5 µL dest. H2O


  • Analysis by agarose gel:
Gelanalysis of PCR 1-4.
Gel analysis of PCR 5-8.


  • PCR-Purification:
    • BS1a (9-38-451) 113.6 ng/µL
    • BS1b (9-38-452) 75.1 ng/µL
    • BS2a (9-38-453) 85.5 ng/µL
    • BS3a (9-38-454) 107.6 ng/µL
    • BS4a (9-38-455) 14.4 ng/µL
    • BS5a (9-38-456) 44.5 ng/µL
    • BS5b (9-38-457) 49.0 ng/µL
    • BS6a (9-38-458) 63.6 ng/µL
    • BS7a (9-38-459) 6.9 ng/µL
    • BS8a (9-38-460) 8.6 ng/µL


  • Successful PCR on the BBa_J04450 BioBrick plasmid using part specific forward and reverse primer (Week 12) for later Gibson Assembly. Isolation of the pSB1C3 PCR product by agarose gel electrophoresis and gel extraction.
  • Gibson Assembly, using the different new pSB1C3 PCR products and the according gene-cluster PCR products.