"
Team:LMU-Munich/Weekly Journal
From 2012.igem.org
| Line 47: | Line 47: | ||
<img src="https://static.igem.org/mediawiki/2012/8/8d/Bacilluss_Intro.png" height=40"/></a></html> | <img src="https://static.igem.org/mediawiki/2012/8/8d/Bacilluss_Intro.png" height=40"/></a></html> | ||
--> | --> | ||
| + | |||
| + | <div class="box" style= "background-color:#e4f1d7"> | ||
| + | ===Septmeber''=== | ||
| + | </div> | ||
| + | |||
<div class="box"> | <div class="box"> | ||
'''24-28 September 2012''' | '''24-28 September 2012''' | ||
</div> | </div> | ||
| + | |||
<div class="box"> | <div class="box"> | ||
'''17-21 September 2012''' | '''17-21 September 2012''' | ||
</div> | </div> | ||
| + | |||
<div class="box"> | <div class="box"> | ||
'''10-14 September 2012''' | '''10-14 September 2012''' | ||
| Line 60: | Line 67: | ||
To clean up our '''Sporo'''beads from vegetative ''B. subtilis'' cells we tried three different methods: French Press, sonification and lysozymes. A significant 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! | To clean up our '''Sporo'''beads from vegetative ''B. subtilis'' cells we tried three different methods: French Press, sonification and lysozymes. A significant 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! | ||
</div> | </div> | ||
| + | |||
<div class="box"> | <div class="box"> | ||
'''3-7 September 2012''' | '''3-7 September 2012''' | ||
| Line 73: | Line 81: | ||
<html><a><img src="https://static.igem.org/mediawiki/2012/7/78/BacillusBioBrickBox.png" height=40"/></a></html> 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. | <html><a><img src="https://static.igem.org/mediawiki/2012/7/78/BacillusBioBrickBox.png" height=40"/></a></html> 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. | ||
</div> | </div> | ||
| + | |||
| + | <div class="box" style= "background-color:#e4f1d7"> | ||
| + | ===August''=== | ||
| + | </div> | ||
| + | |||
<div class="box"> | <div class="box"> | ||
'''26-31 August 2012''' | '''26-31 August 2012''' | ||
| Line 93: | Line 106: | ||
The genes [http://partsregistry.org/wiki/index.php?title=Part:BBa_K823028 luc+] and [http://partsregistry.org/wiki/index.php?title=Part:BBa_K823029 mKate2], synthesized by [https://2012.igem.org/Team:LMU-Munich/Sponsors GeneArt] were successfully cloned into pSB1C3 and sequenced. | The genes [http://partsregistry.org/wiki/index.php?title=Part:BBa_K823028 luc+] and [http://partsregistry.org/wiki/index.php?title=Part:BBa_K823029 mKate2], synthesized by [https://2012.igem.org/Team:LMU-Munich/Sponsors GeneArt] were successfully cloned into pSB1C3 and sequenced. | ||
</div> | </div> | ||
| + | |||
<div class="box"> | <div class="box"> | ||
'''20-24 August 2012''' | '''20-24 August 2012''' | ||
| Line 106: | Line 120: | ||
</div> | </div> | ||
| + | |||
<div class="box"> | <div class="box"> | ||
'''13-17 August 2012''' | '''13-17 August 2012''' | ||
| Line 119: | Line 134: | ||
The xylose-inducible promoter with the according repressor (which has a constitutive promoter, RBS and terminator) P<sub><i>Xyl</i></sub> + <i>XylR</i> was cloned into pSB1C3 and sequenced. | The xylose-inducible promoter with the according repressor (which has a constitutive promoter, RBS and terminator) P<sub><i>Xyl</i></sub> + <i>XylR</i> was cloned into pSB1C3 and sequenced. | ||
</div> | </div> | ||
| + | |||
<div class="box"> | <div class="box"> | ||
'''6-10 August 2012''' | '''6-10 August 2012''' | ||
Revision as of 10:40, 15 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
|
|
Septmeber
24-28 September 2012
17-21 September 2012
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 significant 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!
3-7 September 2012
All our CotZ-GFP variants were examined with fluorescence microscopy! The brightest spores derived from our Pyz-CotZrep-GFP-T mutants!
Plates of our spores diluted at 10-2, 10-4 and 10-6 from the germination assay show NO GERMINATION for our triple and quadruple mutants, and plenty of germination for the WT168 positive control! We will try plating undiluted mutant spores to see if any germination occurs.
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.
Jara created quadruple mutants using two variations on past mutants: cwlD::kan + cwlJ::spec + gerD::cat + sleB::mls and gerD::cat + sleB::mls + cwlJ::spec + cwlD::kan.
Germination assay was performed on triple and quadruple mutants.
The BioBrick [http://partsregistry.org/wiki/index.php?title=Part:BBa_K823019 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 [http://partsregistry.org/wiki/index.php?title=Part:BBa_K823028 luc+] and [http://partsregistry.org/wiki/index.php?title=Part:BBa_K823029 mKate2], synthesized by GeneArt were successfully cloned into pSB1C3 and sequenced.
20-24 August 2012
Double negative loop with lacZa was finished and works qualitatively (Julia).
Finally we could start with the PcgeA evaluation! Contrary to our expectations it did not show any activity :(
13-17 August 2012
Jara and Jenny used last week's double mutants to create triple mutants as follows: cwlD::kan + sleB::mls + cwlJ::spec ; cwlD::kan + sleB::mls + gerD::cat ; cwlD::kan + cwlJ::spec + gerD::cat ; gerD::cat + sleB::mls + cwlJ::spec.
ß-glactosiase assay of the Anderson promoters J23100, J23102, J23103, J23106 in pSBBs1C-lacZ in B. subtilis.
The xylose-inducible promoter with the according repressor (which has a constitutive promoter, RBS and terminator) PXyl + XylR was cloned into pSB1C3 and sequenced.
6-10 August 2012
Jara and Jenny created four double-mutants using resistance-cassettes to knock out germination genes as follows: cwlD::kan + sleB::mls ; gerD::cat + sleB::mls ; gerD::cat + cwlD::kan ; cwlJ::spec + cwlD::kan. 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.
30 July - 3 August 2012
23-27 July 2012
Plate reader measurements of the Bacillus promoters PliaG, PliaI and PlepA finished. Look at Data!
16-20 July 2012
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!
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 red colony color.
2-6 July 2012
Clean deletions of germination genes sleB and cwlB from PCR accomplished. DNA purified and frozen to be later transformed with Bacillus.
β-galactosidase assays of the promoters PliaG, PliaI and 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.
25-29 June 2012
18-22 June 2012
11-15 June 2012
Clean deletions of germination genes cwlD, cwlJ, and gerD from PCR accomplished. DNA purified and frozen to be later transformed with Bacillus.
4-8 June 2012
28-1 June 2012
21-25 May 2012
Promoters PliaG, PliaI, Pveg and PlepA are now in the vector pSB1C3 as BioBrick standard for the registry. BioBricks are BBa_K823000, BBa_K823001, BBa_K823002, BBa_K823003.
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
7-11 May 2012
Cloning of PliaG, PliaI and Pveg in vector pSBBs1C-lacZ finished.
30 April-4 Mai 2012
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 cloning of the reporter vector pSBBs1C-lacZ was finished.
9-13 April 2012
Jara created the single mutant cwlD::kan.
2-6 April 2012
Jara successfully created our first single knockouts of germination genes using a resistance cassettes: sleB::mls, gerD::cat and cwlJ::spec.
Jara 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.
26-30 March 2012
Jara tried knocking out cwlB using the tet resistance cassette. Mutants of cwlB::tet grew very poorly.
19-23 March 2012
We decided which genes to knock out for the germination stop. Based on the work of [http://www.ncbi.nlm.nih.gov/pubmed/19554258 J. Kim and W. Schumann (2009)], we decided to knock out genes cwlB, gerD, cwlJ, and sleB. From the research of [http://www.ncbi.nlm.nih.gov/pubmed/11466293 B. Setlow et al (2001)], we also chose cwlD.
12-16 March 2012
5-9 March 2012
27 February - 2 March 2012
20-24 February 2012
Team fully formed!
Antibiotic abbreviation legend:
cat: chloramphenicol
kan: kanamycin
mls: Macrolide-Lincosamide-Streptogramin B
spec: spectinomycin
tet: tetracycline
