Revision as of 15:00, 26 September 2013

lux pL controlled luxR with lux pR controlled ndh (LVA-tag) coding for NADH dehydrogenase II

Description

This part is made up of a quorum sensing promoter (BBa_F2621) and ndh gene with a LAV-tag. Under control of the quorum sensing promoter, ndh gene will express periodically as the promoter is periodically activated and repressed. Since the ndh gene is described detailed in Part: BBa_K1036001, here is a detailed description of quorum sensing promoter. Firstly, we should be familiar with the quorum sensing mechanism, the luxI gene is at low expression level and produces LuxI protein that synthesizes a kind of acyl-homoserine lactone (AHL), which is a small molecule that can diffuse across the cell membrane and mediate intercellular coupling when it reaches the threshold as enough biomass accumulated. AHL will bind intracellular protein LuxR, which is also consecutively produced by luxR gene. The LuxR-AHL complex can activate the luxI promoter, and the positive feedback loop is built. However, since in this circuit the luxI gene behind the luxI promoter is changed into ndh gene (with LVA-tag), so it could only be activated by AHL produced by luxI gene on another plasmid, which contains Part: BBa_K1036003.

This year our team designed a synchronous oscillator which contained three main parts(Fig.2). The first part was pSB1C3-gfp-luxI which part was BBa_K1036003 with pSB1C3 backbone. The second one was pSB3T5-aiiA which part was BBa_K546001 with pSB3T5 backbone. The last one was pSB4K5-ndh which part was BBa_K1036000 with pSB4T5 backbone.

Experimental Data

To test the expression of ndh gene, an experiment was designed. The strain E. coli BL21(wide type) carried plasmid pSB4K5-ndh was cultured in LB medium with 25 μg/ml kanamycin under the condition of 37^oC,200 rpm for 12hr.

Sequence and Features