Team:ETH Zurich/Biology/Journal
From 2011.igem.org
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- | {{:Team:ETH Zurich/Templates/ | + | {{:Team:ETH Zurich/Templates/HeaderNew}} |
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
+ | = Lab Journal = | ||
+ | '''Here you can follow the progress of our project as it is coming together.''' | ||
+ | {{:Team:ETH Zurich/Templates/SectionEnd}} | ||
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
== '''Week 1: 20.6-26.6''' == | == '''Week 1: 20.6-26.6''' == | ||
- | |||
* First meeting | * First meeting | ||
- | * Brainstorming | + | * [[Team:ETH_Zurich/Team/Brainstorming|Brainstorming]] |
- | + | {{:Team:ETH Zurich/Templates/SectionEnd}} | |
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
== ''' Week 2: 27.6-3.7''' == | == ''' Week 2: 27.6-3.7''' == | ||
+ | * [[Team:ETH_Zurich/Team/Brainstorming|Brainstorming]] | ||
+ | {{:Team:ETH Zurich/Templates/SectionEnd}} | ||
- | + | {{:Team:ETH Zurich/Templates/SectionStart}} | |
- | + | ||
- | + | ||
== ''' Week 3: 4.7-10.7''' == | == ''' Week 3: 4.7-10.7''' == | ||
* Working on the design of the system | * Working on the design of the system | ||
- | * Design of several Operons for AlcR and several PCR | + | <gallery widths=300px heights=200px> |
+ | File:IMG_5009.JPG | ||
+ | File:IMG 5010.jpg | ||
+ | </gallery> | ||
+ | |||
+ | * Design of several Operons for AlcR and several PCR primers | ||
+ | {{:Team:ETH Zurich/Templates/SectionEnd}} | ||
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
== '''Week 4: 11.7-17.7''' == | == '''Week 4: 11.7-17.7''' == | ||
- | * Ordering of the LacI<sub>M1</sub> and | + | * Ordering of the LacI<sub>M1</sub> and codon-optimized AlcR gene |
* Making of competent DH5-α cells | * Making of competent DH5-α cells | ||
* Cloning of the AlcR-testsystem | * Cloning of the AlcR-testsystem | ||
+ | {{:Team:ETH Zurich/Templates/SectionEnd}} | ||
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
== '''Week 5: 18.7-24.7''' == | == '''Week 5: 18.7-24.7''' == | ||
* First test of the AlcR-system in 96-well plates | * First test of the AlcR-system in 96-well plates | ||
- | + | {{:Team:ETH Zurich/Templates/SectionEnd}} | |
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
== '''Week 6: 25.7-31.7''' == | == '''Week 6: 25.7-31.7''' == | ||
* Transformation of the parts from the iGEM plates | * Transformation of the parts from the iGEM plates | ||
- | + | {{:Team:ETH Zurich/Templates/SectionEnd}} | |
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
== '''Week 7: 1.8-7.8''' == | == '''Week 7: 1.8-7.8''' == | ||
Line 37: | Line 53: | ||
* Ligation and Transformation of | * Ligation and Transformation of | ||
- | ** | + | ** P<sub>R</sub> and luxI |
- | ** | + | ** P<sub>R</sub> and lacI |
** P<sub>lac</sub> and GFP<sub>LVA</sub> | ** P<sub>lac</sub> and GFP<sub>LVA</sub> | ||
** P<sub>lux</sub> and mCherry | ** P<sub>lux</sub> and mCherry | ||
Line 45: | Line 61: | ||
* First meeting with Dr. Oliver Frey (Bio engineering laboratory, Prof. Andreas Hierlemann, D-BSSE ETHZ) to exchange ideas about microfluidic design | * First meeting with Dr. Oliver Frey (Bio engineering laboratory, Prof. Andreas Hierlemann, D-BSSE ETHZ) to exchange ideas about microfluidic design | ||
- | + | {{:Team:ETH Zurich/Templates/SectionEnd}} | |
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
== '''Week 8: 8.8-14.8''' == | == '''Week 8: 8.8-14.8''' == | ||
+ | [[File:Lab5.jpg|right|300px]] | ||
* Synthesized LacI<sub>M1</sub> Gen arrived | * Synthesized LacI<sub>M1</sub> Gen arrived | ||
Line 57: | Line 75: | ||
** P<sub>tet</sub> and LacI<sub>M1</sub> | ** P<sub>tet</sub> and LacI<sub>M1</sub> | ||
** P<sub>tet</sub>-LacI<sub>M1</sub> and Terminator | ** P<sub>tet</sub>-LacI<sub>M1</sub> and Terminator | ||
- | |||
* Improving of the testsystem | * Improving of the testsystem | ||
- | ** Exchange of | + | ** Exchange of some rare codons in AlcR by PCR |
- | ** His-tagging of AlcR | + | ** His-tagging of AlcR for detection in Western blot |
- | ** | + | ** include sfGFP |
- | * Transformation of | + | * Transformation of P<sub>R</sub> |
- | * | + | * Creation of competent JM101 cells |
** Check for transformation efficiency | ** Check for transformation efficiency | ||
- | + | {{:Team:ETH Zurich/Templates/SectionEnd}} | |
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
== '''Week 9: 15.8-21.8''' == | == '''Week 9: 15.8-21.8''' == | ||
- | + | [[File:IMG 6171 Kopie.JPG|right|300px]] | |
* Growth and repression test of AlcR-system with M9-medium | * Growth and repression test of AlcR-system with M9-medium | ||
* Ligation and Transformation of | * Ligation and Transformation of | ||
- | ** | + | ** P<sub>R</sub> and lacI |
- | ** | + | ** P<sub>R</sub> and luxI |
** P<sub>tet</sub> and CI | ** P<sub>tet</sub> and CI | ||
- | ** | + | ** P<sub>R</sub>-lacI and terminator |
- | ** | + | ** P<sub>R</sub>-luxI and terminator |
+ | {{:Team:ETH Zurich/Templates/SectionEnd}} | ||
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
== '''Week 10: 22.8-28.8''' == | == '''Week 10: 22.8-28.8''' == | ||
+ | * Transformation and Ligation | ||
+ | ** P<sub>tet</sub>-CI and Terminator | ||
+ | * Preparation of chemically competent DH5-α and JM101 cells | ||
+ | {{:Team:ETH Zurich/Templates/SectionEnd}} | ||
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
+ | == '''Week 11: 29.8-4.9''' == | ||
+ | * Transformation and Ligation | ||
+ | ** P<sub>tet</sub>-CI and Terminator | ||
+ | * Diffusion test through tube system filled with agarose and cells | ||
+ | * Test of the improved AlcR system | ||
+ | {{:Team:ETH Zurich/Templates/SectionEnd}} | ||
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
+ | == '''Week 12: 5.9.-11.9''' == | ||
+ | [[File:Lab6.JPG|right|300px]] | ||
+ | |||
+ | *Design of a system to characterize our new biobrick LacI<sub>M1</sub> | ||
+ | **Transformation and Ligation | ||
+ | *** P<sub>Tet</sub> and LacI | ||
+ | *** P<sub>Lac</sub> and GFP assam | ||
+ | |||
+ | *Design of an additional construct to test the band pass filter | ||
+ | **Transformation and Ligation | ||
+ | ***P<sub>const</sub> and TetR<sub>LVA</sub> | ||
+ | |||
+ | *Growth-test of ''E. coli'' in M9 with reduced Ampicillin concentration | ||
+ | |||
+ | *AlcR test with reduced Ampicillin concentration | ||
+ | |||
+ | *Testdigest of λP-luxI-Terminator | ||
+ | |||
+ | *Alternative Sensor system: Xylene system | ||
+ | **Transformation and Ligation | ||
+ | *** P<sub>const</sub> and XylR | ||
+ | *** P<sub>Xyl</sub> and CI | ||
+ | *** P<sub>Xyl</sub> and LacI <sub>M1</sub> | ||
+ | {{:Team:ETH Zurich/Templates/SectionEnd}} | ||
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
+ | |||
+ | == '''Week 13: 12.9.-18.9''' == | ||
+ | [[File:IMG 6442.JPG|right|300px]] | ||
+ | * PCR of the pBR322 Ori | ||
+ | * PCR of the gen cluster for the upper TOL pathway | ||
+ | * first test of cell printing | ||
+ | *Transformation and Ligation of | ||
+ | ** P<sub>const</sub>-TetR- P<sub>Tet</sub>-LacI<sub>M1</sub> and P<sub>R</sub>-GFPassam | ||
+ | * Western Blot of AlcR | ||
+ | * Making of competent DH5-α cells | ||
+ | * Design and construction of Psb6A5 | ||
+ | {{:Team:ETH Zurich/Templates/SectionEnd}} | ||
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
+ | |||
+ | == '''Week 14: 19.9.-25.9''' == | ||
+ | * Characterization of LacI<sub>M1</sub> | ||
+ | * Cloning of all biobricks into pSB1C3 | ||
+ | * PCR of LacI and CI | ||
+ | * wiki | ||
+ | {{:Team:ETH Zurich/Templates/SectionEnd}} | ||
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
+ | == '''Week 15: 26.9.-02.10''' == | ||
+ | [[File:IMG 6649.JPG|right|300px]] | ||
+ | * design of Pu promoter | ||
+ | * test of Pu promoter | ||
+ | * test for indol degradation | ||
+ | * Poster | ||
+ | * Preparing the presentation | ||
+ | {{:Team:ETH Zurich/Templates/SectionEnd}} | ||
+ | |||
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
+ | |||
+ | == '''European Jamboree 30.9-2.10''' == | ||
+ | * Sightseeing and having fun in Amsterdam | ||
+ | * Gold Medal | ||
+ | * Honorable Mention in category ''Best Model'' | ||
+ | * [https://2011.igem.org/Jamborees Jamboree] | ||
+ | {{:Team:ETH Zurich/Templates/SectionEnd}} | ||
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
+ | |||
+ | == '''Week 16: 03.10.-09.10''' == | ||
+ | * proof of concept with an arabinose inducable system | ||
+ | * cloning for the xylene system | ||
+ | * cloning of the lac-testsystem to compaire LacI<sub>M1</sub> | ||
+ | {{:Team:ETH Zurich/Templates/SectionEnd}} | ||
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
+ | == '''Week 17: 10.10.-16.10''' == | ||
+ | * cloning of the alarm-test system | ||
+ | * cloning the final system with xylene | ||
+ | * cloning the arabinose system | ||
+ | * cloning the AlcR (codon optimized) system | ||
+ | * building a channel out of different materials | ||
+ | * Design a assay for testing the alarm system | ||
+ | * Sender receiver test on plates | ||
+ | {{:Team:ETH Zurich/Templates/SectionEnd}} | ||
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
+ | |||
+ | == '''Week 18: 17.10.-23.10''' == | ||
+ | * Cloning | ||
+ | * inactivating of the kanamycin casette of BW27749 to get BW27783 | ||
+ | * Make competent BW27783 and DH5-α cells | ||
+ | * Sender receiver test on plates with sterile filtrated supernatant | ||
+ | * Sender an receiver test in tube | ||
+ | * Dose response experiment for xylene | ||
+ | * Dose response experiment for acetaldehyde | ||
+ | {{:Team:ETH Zurich/Templates/SectionEnd}} | ||
+ | {{:Team:ETH Zurich/Templates/SectionStart}} | ||
+ | |||
+ | == '''Week 19: 24.10-30.10''' == | ||
+ | * Cloning | ||
+ | * Microscope experiments of the channel with and without degradation | ||
+ | * Alarm test with AHL | ||
+ | * Dose response experiment for acetaldehyde | ||
+ | * Dose response experiment for arabinose | ||
+ | {{:Team:ETH Zurich/Templates/SectionEnd}} | ||
+ | {{:Team:ETH Zurich/Templates/HeaderNewEnd}} |
Latest revision as of 19:50, 27 October 2011
Lab Journal
Here you can follow the progress of our project as it is coming together.
Week 3: 4.7-10.7
- Working on the design of the system
- Design of several Operons for AlcR and several PCR primers
Week 4: 11.7-17.7
- Ordering of the LacIM1 and codon-optimized AlcR gene
- Making of competent DH5-α cells
- Cloning of the AlcR-testsystem
Week 5: 18.7-24.7
- First test of the AlcR-system in 96-well plates
Week 6: 25.7-31.7
- Transformation of the parts from the iGEM plates
Week 7: 1.8-7.8
- Growth test of DH5-α with AlcR-system in flasks
- Ligation and Transformation of
- PR and luxI
- PR and lacI
- Plac and GFPLVA
- Plux and mCherry
- Ptet and CI -had to be redone because of point mutation in the primer (week 9)
- Pconst and luxR
- First meeting with Dr. Oliver Frey (Bio engineering laboratory, Prof. Andreas Hierlemann, D-BSSE ETHZ) to exchange ideas about microfluidic design
Week 8: 8.8-14.8
- Synthesized LacIM1 Gen arrived
- Ligation and Transformation of
- Plac-GFPLVA and Terminator
- Plux-mCherry and Terminator
- Pconst-luxR and Terminator
- Plac-GFPLVA-Terminator and Plux-mCherry-Terminator on one plasmid
- Ptet and LacIM1
- Ptet-LacIM1 and Terminator
- Improving of the testsystem
- Exchange of some rare codons in AlcR by PCR
- His-tagging of AlcR for detection in Western blot
- include sfGFP
- Transformation of PR
- Creation of competent JM101 cells
- Check for transformation efficiency
Week 9: 15.8-21.8
- Growth and repression test of AlcR-system with M9-medium
- Ligation and Transformation of
- PR and lacI
- PR and luxI
- Ptet and CI
- PR-lacI and terminator
- PR-luxI and terminator
Week 10: 22.8-28.8
- Transformation and Ligation
- Ptet-CI and Terminator
- Preparation of chemically competent DH5-α and JM101 cells
Week 11: 29.8-4.9
- Transformation and Ligation
- Ptet-CI and Terminator
- Diffusion test through tube system filled with agarose and cells
- Test of the improved AlcR system
Week 12: 5.9.-11.9
- Design of a system to characterize our new biobrick LacIM1
- Transformation and Ligation
- PTet and LacI
- PLac and GFP assam
- Transformation and Ligation
- Design of an additional construct to test the band pass filter
- Transformation and Ligation
- Pconst and TetRLVA
- Transformation and Ligation
- Growth-test of E. coli in M9 with reduced Ampicillin concentration
- AlcR test with reduced Ampicillin concentration
- Testdigest of λP-luxI-Terminator
- Alternative Sensor system: Xylene system
- Transformation and Ligation
- Pconst and XylR
- PXyl and CI
- PXyl and LacI M1
- Transformation and Ligation
Week 13: 12.9.-18.9
- PCR of the pBR322 Ori
- PCR of the gen cluster for the upper TOL pathway
- first test of cell printing
- Transformation and Ligation of
- Pconst-TetR- PTet-LacIM1 and PR-GFPassam
- Western Blot of AlcR
- Making of competent DH5-α cells
- Design and construction of Psb6A5
Week 14: 19.9.-25.9
- Characterization of LacIM1
- Cloning of all biobricks into pSB1C3
- PCR of LacI and CI
- wiki
Week 15: 26.9.-02.10
- design of Pu promoter
- test of Pu promoter
- test for indol degradation
- Poster
- Preparing the presentation
European Jamboree 30.9-2.10
- Sightseeing and having fun in Amsterdam
- Gold Medal
- Honorable Mention in category Best Model
- Jamboree
Week 16: 03.10.-09.10
- proof of concept with an arabinose inducable system
- cloning for the xylene system
- cloning of the lac-testsystem to compaire LacIM1
Week 17: 10.10.-16.10
- cloning of the alarm-test system
- cloning the final system with xylene
- cloning the arabinose system
- cloning the AlcR (codon optimized) system
- building a channel out of different materials
- Design a assay for testing the alarm system
- Sender receiver test on plates
Week 18: 17.10.-23.10
- Cloning
- inactivating of the kanamycin casette of BW27749 to get BW27783
- Make competent BW27783 and DH5-α cells
- Sender receiver test on plates with sterile filtrated supernatant
- Sender an receiver test in tube
- Dose response experiment for xylene
- Dose response experiment for acetaldehyde
Week 19: 24.10-30.10
- Cloning
- Microscope experiments of the channel with and without degradation
- Alarm test with AHL
- Dose response experiment for acetaldehyde
- Dose response experiment for arabinose