Team:LMU-Munich/Weekly Journal

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Revision as of 12:28, 7 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

Legend:

+--+--+--+--+--+--	+--+--+--+--+--	+--+--+--+--+--+--	+--+--+--+--+--+--
Bacillus Intro	Bacillus BioBrickBOX	SporeCoat FusionProteins	Germination STOP

	3-7 September 2012
	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 WT positive control! We will try plating undiluted mutant spores to see if any germination occurs.	A collection of useful tags in Freiburgs standard and with RBS included was cloned into pSB1C3. The tags are: 3xFlag, HA, cMyc, 10xHis and Streptavidin.
	26-31 August 2012
	Finally, we got our first glowing spore!! After 4 months of hard work we have our first proof that our system 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 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 pSB_Bs0K-P_spac 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 gene art were succesfully cloned into pSB1C3 and sequenced.	20-24 August 2012
	Double negative loop with lacZa finished -> works qualitatively (Julia)
	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 pSB_Bs1C-lacZ in B. subtilis. The xylose-inducible promoter with the according repressor (which has a constitutive promoter, RBS and terminator) P_{Xyl</> + <i>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 pSB_Bs3C-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 P_liaG, P_liaI and P_lepA 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 pSB_Bs3C-luxABCDE completed. Look at Data!

Cloning of the Anderson promoters J23100, J23102, J23103, J23106 in the reporter vector pSB_Bs1C-lacZ for β-galactosidase assays finished.

9-13 July 2012 The vectors pSB_Bs4S-P_Xyl , pSB_Bs1C-lacZ and pSB_Bs4S were succesfully completed and tested by restriction digest as well as red colony colour.

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 P_liaG, P_liaI and P_veg 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 P_liaG, P_liaI, P_veg and P_lepA 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 pSB_Bs3C-luxABCDE for measuring their activity as luminescence.

The Bacillus promoters P_liaG, P_liaI and P_lepA are in the Bacillus reporter vector pSB_Bs3C-luxABCDE.

14-18 May 2012

7-11 May 2012

Cloning of P_liaG, P_liaI and P_veg in vector pSB_Bs1C-lacZ finished.

30 April-4 Mai 2012

23-27 April 2012 pSB_Bs3C-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 pSB_Bs1C-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 pSB_Bs0K-P_spac 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

Retrieved from "http://2012.igem.org/Team:LMU-Munich/Weekly_Journal"

@@ Line 73: / Line 73: @@
 |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 WT positive control! We will try plating undiluted mutant spores to see if any germination occurs.
 |
+<html><a><img src="https://static.igem.org/mediawiki/2012/7/78/BacillusBioBrickBox.png" height=40"/></a></html> A collection of useful tags in Freiburgs standard and with RBS included was cloned into pSB1C3. The tags are: 3xFlag, HA, cMyc, 10xHis and Streptavidin.
 |-
@@ Line 89: / Line 91: @@
 |-
 |
+<html><a><img src="https://static.igem.org/mediawiki/2012/7/78/BacillusBioBrickBox.png" height=40"/></a></html> The BioBrick [http://partsregistry.org/wiki/index.php?title=Part:BBa_K823019 lacZ] for ''B. subtilis'' was shown to be functional in <b>pSB<sub>Bs</sub>0K-P<sub><i>spac</i></sub> </b> 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 gene art were succesfully cloned into pSB1C3 and sequenced.
@@ Line 107: / Line 111: @@
 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.
+<html><a><img src="https://static.igem.org/mediawiki/2012/7/78/BacillusBioBrickBox.png" height=40"/></a></html> ß-glactosiase assay of the Anderson promoters J23100, J23102, J23103, J23106 in <b>pSB<sub>Bs</sub>1C-<i>lacZ</i> </b> in ''B. subtilis''.
+The xylose-inducible promoter with the according repressor (which has a constitutive promoter, RBS and terminator) P<sub><i>Xyl</> + <i>XylR</i> was cloned into pSB1C3 and sequenced.
 |-
 |
@@ Line 115: / Line 121: @@
 <img src="https://static.igem.org/mediawiki/2012/f/f6/GerminationSTOP.png" height=40"/></a></html>
 |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.
+<html><a><img src="https://static.igem.org/mediawiki/2012/7/78/BacillusBioBrickBox.png" height=40"/></a></html> Finally, the last PstI site could be removed and <b>pSB<sub>Bs</sub>3C-<i>luxABCDE</i> </b> was completed.
+Also, the double terminator B0014 was cloned into pSB1C3.
@@ Line 149: / Line 159: @@
 '''9-13 July 2012'''
+<html><a><img src="https://static.igem.org/mediawiki/2012/7/78/BacillusBioBrickBox.png" height=40"/></a></html> The vectors <b>pSB<sub>Bs</sub>4S-P<sub><i>Xyl</i></sub> </b>, <b>pSB<sub>Bs</sub>1C-<i>lacZ</i> </b> and <b>pSB<sub>Bs</sub>4S </b> were succesfully completed and tested by restriction digest as well as red colony colour.
@@ Line 205: / Line 216: @@
 '''23-27 April 2012'''
+<html><a><img src="https://static.igem.org/mediawiki/2012/7/78/BacillusBioBrickBox.png" height=40"/></a></html> <b>pSB<sub>Bs</sub>3C-<i>luxABCDE</i> </b> 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'''
+<html><a><img src="https://static.igem.org/mediawiki/2012/7/78/BacillusBioBrickBox.png" height=40"/></a></html> The cloning of the reporter vector <b>pSB<sub>Bs</sub>1C-<i>lacZ</i> </b> was finished.
 '''9-13 April 2012'''
@@ Line 225: / Line 238: @@
 Jara tried knocking out ''cwlB'' using the kan resistance cassette. Mutants of ''cwlB''::kan grew very poorly.
+<html><a><img src="https://static.igem.org/mediawiki/2012/7/78/BacillusBioBrickBox.png" height=40"/></a></html> With <b>pSB<sub>Bs</sub>0K-P<sub><i>spac</i></sub> </b> our first Vector for our <b>B</b>acillus <b>B</b>io<b>B</b>rick <b>B</b>ox was completed.
 '''26-30 March 2012'''