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Team:LMU-Munich/Weekly Journal
From 2012.igem.org
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<img src="https://static.igem.org/mediawiki/2012/7/78/BacillusBioBrickBox.png" height=40"/></a></html> | <img src="https://static.igem.org/mediawiki/2012/7/78/BacillusBioBrickBox.png" height=40"/></a></html> | ||
| - | Plate reader measurements of the ''Bacillus'' promoters [http://partsregistry.org/Part:BBa_K823000 P<sub>''liaG''</sub>], [http://partsregistry.org/Part:BBa_K823001 P<sub>''liaI''</sub>] and [http://partsregistry.org/Part:BBa_K823002 P<sub>''lepA''</sub>] finished. Look at [https://2012.igem.org/Team:LMU-Munich/Data Data]!</p> | + | Plate reader measurements of the ''Bacillus'' promoters [http://partsregistry.org/Part:BBa_K823000 P<sub>''liaG''</sub>], [http://partsregistry.org/Part:BBa_K823001 P<sub>''liaI''</sub>] and [http://partsregistry.org/Part:BBa_K823002 P<sub>''lepA''</sub>] are finished. Look at [https://2012.igem.org/Team:LMU-Munich/Data Data]!</p> |
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<img src="https://static.igem.org/mediawiki/2012/8/8d/Bacilluss_Intro.png" height=25"/></a></html> | <img src="https://static.igem.org/mediawiki/2012/8/8d/Bacilluss_Intro.png" height=25"/></a></html> | ||
| - | Not many of us are working on our modules this week, as we are helping out for [https://2012.igem.org/Team:LMU-Munich/Human_Practice/CAS_Conference CAS SynBio conference] and organising the [https://2012.igem.org/Team:LMU-Munich/Human_Practice/Students_Practical_Course Students Practical Course].</p> | + | Not many of us are working on our modules this week, as we are helping out for the [https://2012.igem.org/Team:LMU-Munich/Human_Practice/CAS_Conference CAS SynBio conference] and organising the [https://2012.igem.org/Team:LMU-Munich/Human_Practice/Students_Practical_Course Students Practical Course].</p> |
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<p align="justify"><html><a><img src="https://static.igem.org/mediawiki/2012/7/78/BacillusBioBrickBox.png" height=40"/></a></html> | <p align="justify"><html><a><img src="https://static.igem.org/mediawiki/2012/7/78/BacillusBioBrickBox.png" height=40"/></a></html> | ||
| - | The vectors [http://partsregistry.org/Part:BBa_K823024 <b>pSB<sub>Bs</sub>4S-P<sub><i>Xyl</i></sub> </b>], [http://partsregistry.org/Part:BBa_K823021 <b>pSB<sub>''Bs''</sub>1C-''lacZ''</b>] and [http://partsregistry.org/Part:BBa_K823022 <b>pSB<sub>Bs</sub>4S </b>] were succesfully completed and tested by restriction digest as well as red colony color. </p> | + | The vectors [http://partsregistry.org/Part:BBa_K823024 <b>pSB<sub>Bs</sub>4S-P<sub><i>Xyl</i></sub> </b>], [http://partsregistry.org/Part:BBa_K823021 <b>pSB<sub>''Bs''</sub>1C-''lacZ''</b>] and [http://partsregistry.org/Part:BBa_K823022 <b>pSB<sub>Bs</sub>4S </b>] were succesfully completed and tested by restriction digest as well as checked for red colony color. </p> |
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<img src="https://static.igem.org/mediawiki/2012/c/c1/SporeCoat.png" height=40"/></a></html> | <img src="https://static.igem.org/mediawiki/2012/c/c1/SporeCoat.png" height=40"/></a></html> | ||
| - | We started with the clean deletions of CgeA and CotZ this week | + | We started with the clean deletions of CgeA and CotZ this week. It seems like it will take forever if you judge from the protocol length... What took even longer is the pSB<sub>BS</sub>3C-luxABCDE-P<sub>''cgeA''</sub>, but it is finished now!</p> |
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<img src="https://static.igem.org/mediawiki/2012/f/f6/GerminationSTOP.png" height=40"/></a></html> | <img src="https://static.igem.org/mediawiki/2012/f/f6/GerminationSTOP.png" height=40"/></a></html> | ||
| - | In the knockouts part of the '''Germination'''STOP module, clean deletions of germination genes ''sleB'' and ''cwlB'' from PCR were accomplished. DNA purified and frozen to be later transformed with ''Bacillus''.</p> | + | In the knockouts part of the '''Germination'''STOP module, clean deletions of germination genes ''sleB'' and ''cwlB'' from PCR were accomplished. DNA was purified and frozen to be later transformed with ''Bacillus''.</p> |
<p align="justify"><html><a><img src="https://static.igem.org/mediawiki/2012/7/78/BacillusBioBrickBox.png" height=40"/></a></html> | <p align="justify"><html><a><img src="https://static.igem.org/mediawiki/2012/7/78/BacillusBioBrickBox.png" height=40"/></a></html> | ||
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<img src="https://static.igem.org/mediawiki/2012/c/c1/SporeCoat.png" height=40"/></a></html> | <img src="https://static.igem.org/mediawiki/2012/c/c1/SporeCoat.png" height=40"/></a></html> | ||
| - | Our first plate reader experiments with [https://2012.igem.org/Team:LMU-Munich/Data/crustpromoters P<sub>''cotyz''</sub>] and [https://2012.igem.org/Team:LMU-Munich/Data/crustpromoters P<sub>''cotv''</sub>] are running! Like expected they both show activity in the late stationary phase, thus during sporulation!</p> | + | Our first plate reader experiments with [https://2012.igem.org/Team:LMU-Munich/Data/crustpromoters P<sub>''cotyz''</sub>] and [https://2012.igem.org/Team:LMU-Munich/Data/crustpromoters P<sub>''cotv''</sub>] are running! Like expected, they both show activity in the late stationary phase, thus during sporulation!</p> |
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<img src="https://static.igem.org/mediawiki/2012/c/c1/SporeCoat.png" height=40"/></a></html> | <img src="https://static.igem.org/mediawiki/2012/c/c1/SporeCoat.png" height=40"/></a></html> | ||
pSB<sub>''BS''</sub>3C-luxABCDE-P<sub>''cotyz''</sub> and pSB<sub>''BS''</sub>3C-luxABCDE-P<sub>''cotv''</sub> integrated into the ''B. subtilis'' genome! | pSB<sub>''BS''</sub>3C-luxABCDE-P<sub>''cotyz''</sub> and pSB<sub>''BS''</sub>3C-luxABCDE-P<sub>''cotv''</sub> integrated into the ''B. subtilis'' genome! | ||
| - | Bad luck, we found an additional AgeI site in ''cgeA'' | + | Bad luck, we found an additional AgeI site in ''cgeA''. It seems that this is the reason why we could not fuse ''gfp'' to it... Mutagenesis primers are designed and ordered!</p> |
</div> | </div> | ||
Revision as of 15:29, 26 September 2012
The LMU-Munich team is exuberantly happy about the great success at the World Championship Jamboree in Boston. Our project Beadzillus finished 4th and won the prize for the "Best Wiki" (with Slovenia) and "Best New Application Project".
[ more news ]
Weekly Journal
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September
24-28 September 2012
Now, the Sporo vector is cloned into pSBBs4S and we are trying to insert lacZ.
We all are busy setting up our website and finding the best ways to display our results!
Sitting on the computer every day and analyzing the sheer number of microscopy pictures...
17-21 September 2012
Last microscopy experiments with the clean deletion mutants. They are glowing even brighter!
Finished cloning of mKate2 constructs. Now the evaluation of this reporter BioBrick with three different promoters, PliaI, PlepA and the Anderson promoter J23101, can start.
Finished cloning of Sporo vector in pSB1C3.
Evaluation of pSBBs0K-Pspac with lacZ.
Inverter measured quantitively via β-Galactosidase assay.
For our Suicide switch, the first plate reader measurement of Bacillus subtilis strain W168 containing thrC::PspoIVB-ecf41Bli aa 1-204 (through transformation with pSBBs4S-PspoIVB-ecf41Bli aa 1-204) and sacA::PydfG-luxABCDE (through transformation with pSBBs3C-luxABCDE-PydfG) was performed.
Knockouts: One last run of the germination assay on our triple and quadruple mutants. All results of these assays can be found compiled on our data page.
10-14 September 2012
To clean up our Sporobeads from vegetative B. subtilis cells we tried three different methods: French Press, sonification and lysozymes. A great difference was observed after the treatment with lysozyme! Furthermore, the lysozyme did not damage our fusion protein, as GFP fluorescence was still obtained in microscopy!
PlepA was fused into the finished vector pSBBS3C-luxABCDE to evaluate this BioBrick vector and compare in to the version where there is still one forbidden restriction site in it.
For the Suicide switch, PspoIVB-ecf41Bli aa 1-204 in pSBBS4S, and PydfG/PsspK/PspoIVB in pSBBS3C-luxABCDE were brought into B. subtilis.
More work on the knockouts: We were really surprised at our great results so far, and repeated the germination assay on our triple and quadruple mutants once again.
3-7 September 2012
All of our CotZ-GFP variants were examined with fluorescence microscopy! The brightest spores derived from our Pcotyz-cotZrep-gfp-terminator mutants.
We worked more on the knockouts aspect of the GerminationSTOP module. We ran another germination assay for our triple and quadruple mutants. Plates of our spores diluted at 10-2, 10-4 and 10-6 show NO GERMINATION for our mutants, and plenty of germination for the WT168 positive control! We will try plating undiluted mutant spores to see if any germination occurs at higher concentrations.
More work on the Suicide switch! PsspK, PspoIVB and PydfG were cloned into pSB1C3 and verified by sequencing.
PspoIVB-ecf41Bli aa1-204 were cloned into pSBBS4S and verified by sequencing.
PydfG/PsspK/PspoIVB were brought into pSBBS3C-luxABCDE.
lacZ was succesfully cloned into pSBBs4S-PXyl and is functional (blue colonies with IPTG and X-Gal).
A collection of useful tags in Freiburg standard and with RBS included was cloned into pSB1C3. The tags are: 3xFlag, HA, cMyc, 10xHis and Streptavidin.
August
26-31 August 2012
Finally, we got our first glowing spores!! After 4 months of hard work, we have the first proof that this module works.
More on germination knockouts -- we created quadruple mutants using two variations on past mutants: cwlD::kan + cwlJ::spec + gerD::cm + sleB::mls and gerD::cm + sleB::mls + cwlJ::spec + cwlD::kan. See our Strains Collection.
Germination assay was performed on triple and quadruple mutants.
For the Suicide switch, MazF and Ecf41Bli aa 1-204 were cloned into pSB1C3 and verified by sequencing.
The BioBrick lacZ for B. subtilis was shown to be functional in pSBBs0K-Pspac in E. coli and B. subtilis (blue color on plates with IPTG and X-Gal).
The genes luc+ and mKate2, synthesized by GeneArt, were successfully cloned into pSB1C3 and sequenced.
20-24 August 2012
Inverter with lacZα was finished and it works qualitatively.
Good and bad news this week. First the good news: Another big step towards the GFP-Sporobeads is done! We have the CotZ constructs in pSBBS1C! Hopefully it will integrate easily! :D
Now the bad news: Finally we could start with the PcgeA evaluation! But contrary to our expectations, this promoter did not show any activity.
13-17 August 2012
For the knockouts, we used last week's double mutants to create triple mutants as follows: cwlD::kan + sleB::mls + cwlJ::spec ; cwlD::kan + sleB::mls + gerD::cm ; cwlD::kan + cwlJ::spec + gerD::cm ; and gerD::cm + sleB::mls + cwlJ::spec. See our Strains Collection.
ß-glactosidase assay of the Anderson promoters J23100, J23102, J23103 in pSBBs1C-lacZ in B. subtilis was performed.
The xylose-inducible promoter with the according repressor (which has a constitutive promoter, RBS and terminator) xylR-PXyl was cloned into pSB1C3 and sequenced.
At last Bacillus was keen on integrating the pSBBS3C-luxABCDE-PcgeA!! And the clean deletions of CotZ and CgeA worked out, too!
6-10 August 2012
Germination knockouts: We created four double-mutants using resistance-cassettes to knock out germination genes as follows: cwlD::kan + sleB::mls ; gerD::cm + sleB::mls ; gerD::cm + cwlD::kan ; cwlJ::spec + cwlD::kan. See our Strains Collection. Of these double mutants, we tested three strains in our germination assay. We also created the resistance cassette knockout cwlB::kan.
Finally, the last PstI site could be removed and pSBBs3C-luxABCDE was completed.
Also, the double terminator B0014 was cloned into pSB1C3.
The final Promoter-CotZ-GFP-Terminator constructs in pSB1C3 are ready!! Our Promoter-CgeAmut constructs are finally finished too.
July
30 July - 3 August 2012
GFP-Terminator is ready for use and the AgeI site in CgeA is mutated!
23-27 July 2012
This week is our Human Practice week!
From the 23rd to 25th of July we enjoyed the CAS SynBio conference and the visit of 10 iGEM teams!
This weekend, high school students participated in our Students Practical Course for three days and developed their ideas for useful Sporobeads!
It was a great week!
Plate reader measurements of the Bacillus promoters PliaG, PliaI and PlepA are finished. Look at Data!
16-20 July 2012
Not many of us are working on our modules this week, as we are helping out for the CAS SynBio conference and organising the Students Practical Course.
Plate reader measurements of the Anderson promoters J23100, J23101, J23102, J23103, J23106, J23107, J23113, J23114, J23115,
J23117, J23118 in the Bacillus reporter vector pSBBs3C-luxABCDE completed. Look at Data Anderson promoters!
Cloning of the Anderson promoters J23100, J23102, J23103, J23106 in the reporter vector pSBBs1C-lacZ for β-galactosidase assays finished.
9-13 July 2012
The vectors pSBBs4S-PXyl , pSBBs1C-lacZ and pSBBs4S were succesfully completed and tested by restriction digest as well as checked for red colony color.
We started with the clean deletions of CgeA and CotZ this week. It seems like it will take forever if you judge from the protocol length... What took even longer is the pSBBS3C-luxABCDE-PcgeA, but it is finished now!
2-6 July 2012
In the knockouts part of the GerminationSTOP module, clean deletions of germination genes sleB and cwlB from PCR were accomplished. DNA was purified and frozen to be later transformed with Bacillus.
β-galactosidase assays of the promoters PliaG, PliaI, Pveg are finished. Look at Data!
Cloning of the Anderson promoters J23100, J23101, J23102, J23103, J23106, J23107, J23113, J23114, J23115,
J23117, J23118 in pSB1C3 finished.
Our first plate reader experiments with Pcotyz and Pcotv are running! Like expected, they both show activity in the late stationary phase, thus during sporulation!
June
25-29 June 2012
pSBBS3C-luxABCDE-Pcotyz and pSBBS3C-luxABCDE-Pcotv integrated into the B. subtilis genome!
Bad luck, we found an additional AgeI site in cgeA. It seems that this is the reason why we could not fuse gfp to it... Mutagenesis primers are designed and ordered!
18-22 June 2012
CotZ and GFP constructs are finished, now we can try to fuse them together!
11-15 June 2012
Knockouts: Clean deletions of germination genes cwlD, cwlJ, and gerD from PCR accomplished. DNA purified and frozen to be later transformed with Bacillus. Edit: the clean deletions were never used for transformation, but remain ready for future use.
4-8 June 2012
Still working on the Promoter-Gene and now GFP-Terminator constructs!
May
28 May-1 June 2012
GFP in BioBrick standard is readyyyy!
21-25 May 2012
pSBBS3C-luxABCDE-Pcotyz and pSBBS3C-luxABCDE-Pcotv are ready for transformation into Bacillus!
Promoters PliaG, PliaI, Pveg and PlepA are now in the vector pSB1C3 as BioBrick standard for the registry.
The Anderson promoters J23100, J23101, J23102, J23103, J23106, J23107, J23113, J23114, J23115,
J23117, J23118 are now in the Bacillus reporter vector pSBBs3C-luxABCDE for measuring their activity as luminescence.
The Bacillus promoters PliaG, PliaI and PlepA are in the Bacillus reporter vector pSBBs3C-luxABCDE.
14-18 May 2012
Combining the BioBricks and integrating them into different vectors works good! But still there are constructs missing, we'll keep on working! The fusion of the up and down fragment of CotZ finally works!
7-11 May 2012
The last weeks we tried to fuse the up and down fragment of our spore crust gene together for its clean deletion. For CgeA we have the first fused fragments! CotZ needs a little more attention. :)
Cloning of PliaG, PliaI, Pveg and in vector pSBBs1C-lacZ finished.
April
30 April-4 May 2012
We have the first essential BioBricks for this module: pSB1C3-CotZ, pSB1C3-PcotV, pSB1C3-PcotYZ, pSB1C3-PcgeA, pSB1C3-CgeA! Still working on the pSB1C3-GFP.
23-27 April 2012
pSBBs3C-luxABCDE with still one PstI site was created with RFP in the multile cloning site to have a vector for promoter measurments. edit: This PstI site was removed later and only that backbone is submitted to the registry.
16-20 April 2012
The Sporobead team starts the work in the lab!
The cloning of the reporter vector pSBBs1C-lacZ </b> was finished.
9-13 April 2012
We created the single mutant cwlD::kan.
2-6 April 2012
In our germination genes knockout work, we successfully created our first single knockouts of germination genes using a resistance cassettes: sleB::mls, gerD::cm and cwlJ::spec. See our Strains Collection.
We tried knocking out cwlB using the kan resistance cassette. Mutants of cwlB::kan grew very poorly.
With pSBBs0K-Pspac our first vector for our Bacillus BioBrick Box was completed.
March
26-30 March 2012
Knockouts: We tried knocking out cwlB using the tet resistance cassette. Mutants of cwlB::tet grew very poorly.
19-23 March 2012
For our germination gene knockouts, we decided which genes to knock out for the germination stop. Based on the work of J. Kim and W. Schumann (2009), we decided to knock out genes cwlB, gerD, cwlJ, and sleB. From the research of B. Setlow et al (2001), we also chose cwlD.
5-9 March 2012
We spent two full days (and nights) together planning our project in our "iGEM days." The idea of Beadzillus was born, and we got to know each other better as we divided the modules of the project, and learned each others' strengths and experience in different fields such as microbiology, ecology and biochemistry.
February
20-24 February 2012
Team fully formed!
Antibiotic abbreviation legend:
cm: chloramphenicol
kan: kanamycin
mls: Macrolide-Lincosamide-Streptogramin B
spec: spectinomycin
tet: tetracycline
