Team:Oxford/DCMationB

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Revision as of 12:44, 23 July 2014 by Glen47 (Talk | contribs)

Part B: Biosensor Development

Glen and Fran will be tackling this area of the project in the lab while Oliver and Matt will be modelling this system to allow us to design the ideal biosensor. In the native bacterium, Methylobacterium Extorquens DM4, the DCM sensing protein (DCMR) is encoded by a dcmR gene that is opposite to the DCM degrading enzyme DCMA-encoding gene, dcmA.

Oxfordigem dcmrdcma.png

dcmR is thought to encode a repressor protein that binds to the region of DNA between dcmR and dcmA genes. Upon addition of DCM the repression is thought to be relieved and transcription of dcmA can begin. To test this hypothesis we have extracted this inter-gene region and put sfGFP downstream in place of dcmA. In this way we can inducibly express dcmR on another plasmid and then using varying levels of DCM we can investigate the dynamics of dcmR repression in this region. Thus confirming an activation or repression set-up.


Oxfordigem sfGFP.png