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Team:INSA-Lyon/Project/Stage3/Strategy/ompR234
From 2010.igem.org
Design of ompR234
Escherichia coli bacteria into biofilms contain many adherence structures, as curli structures composed by CsgB et CsgA proteins. Laboratory E. coli K12 strain hasn’t naturally got this phenotype. However, we had a mutant K12 MG1655 E. coli strain on which adherence phenotype had been observed. Indeed, there was a mutation in the genome of the bacteria, particularly in the ompR regulatory gene, at the position 234 (réf public!! Et schéma). The corresponding OmpR234 protein strongly activated the csgD promoter, and CsgD protein activated the CsgB et CsgA transcriptions. So, we intended to create an ompR234 coding sequence Biobrick by PCR on this bacteria genome. Chromosomic DNA PHL818 strain had been extracted with DNeasy Blood & Tissue QIAGEN kit.
Primers couple had been designed with iGEM extension, containing iGEM restriction enzymes sites: a forward primer with a perfect RBS (Ribosome Binding Site) and a reverse primer with a double transcription terminator. A PCR product about 790 pb was expected and the good band had been extracted on agarose gel with NucleoSpin Extract II, Macherey-Nagel kit. Then, we made a cloning into Promega pGEMT vector, as a temporary construction. The final goal is the construction of the ompR234 Biobrick, cloned into pSB1C3, in order to ship the new part to iGEM HQ.
We aimed to make the following construction: constitutive promoter and ompR234 CDS, cloned into a compatible iGEM plasmid backbone. Finally, we would like to do a double transformation with the regulator and also the curli promoter with β-glucosidase, as a reporter gene. This intermediate step will help us to check the functionality of the both new parts. Indeed, we could measure the glucosidase activity.
