IGEM:Cambridge/2008/Notebook/Bacillus
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| + | =Working with ''B.subtilis''= | ||
| + | Building on the work of the last year's Cambridge iGEM team, we are exploring applications of the gram-positive chassis ''B.subtillis''. Easy to handle and transform, this bacterium is much better to use than ''E.coli'' wherever protein import/export is concerned, e.g. in our signalling project. An important part of our effort is to establish standard protocols and parts to work in ''B.subtillis'', characterise control elements, and develop new vectors. You can find our ''Bacillus'' protocols [[IGEM:Cambridge/2008/Protocols|here]]. | ||
=Creating new Biobrick-compatible ''B.subtilis'' vectors= | =Creating new Biobrick-compatible ''B.subtilis'' vectors= | ||
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B. subtilis Promoters to be Tested: | B. subtilis Promoters to be Tested: | ||
| - | * Pupp - constitutive, found Bacillus cereus. | + | * Pupp - constitutive, found in ''Bacillus cereus''. |
* Ppac - constitutive | * Ppac - constitutive | ||
* Pspac - lactose inducible | * Pspac - lactose inducible | ||
Revision as of 09:32, 5 September 2008
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Working with B.subtilisBuilding on the work of the last year's Cambridge iGEM team, we are exploring applications of the gram-positive chassis B.subtillis. Easy to handle and transform, this bacterium is much better to use than E.coli wherever protein import/export is concerned, e.g. in our signalling project. An important part of our effort is to establish standard protocols and parts to work in B.subtillis, characterise control elements, and develop new vectors. You can find our Bacillus protocols here. Creating new Biobrick-compatible B.subtilis vectorsWe are using the In-Fusion™ PCR method from ClonTech to create new Biobrick-compatible integrative and episomal vectors. These vectors will allow us to insert Biobricks into the Bacillus subtilis genome at the AmyE locus and as a 3-5 copy plasmid that will replicate autonomously in Bacillus.
Testing B.subtilis promoters and RBSsWe are seeking to test the expression strength and response to inducers in several promoters in B.subtilis, in combination with different Bacillus-specific ribosome binding sites. B. subtilis Promoter Testing with Beta-galactosidase AssayWe are aiming to characterize four different Bacillus subtilis promoters using the beta-galactosidase assay. (Protocol for beta-galactosidase assay as described here B. subtilis Promoters to be Tested:
Links
B. Subtilis Transformation Protcol - Electroporation
Expression and characterization of aiiA gene from Bacillus subtilis BS-1.
Links to Cambridge 2007 Wiki
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