Difference between revisions of "Part:BBa K1529797"

Revision as of 13:21, 23 October 2014

Plux-CmR-RhlI

We constructed this part by combining BBa_K395162, BBa_B0034 and BBa_C0070.

To characterize Plux-CmR-RhlI (BBa_K1529797), we introduced Plux-CmR-RhlI on pSB3K3 with Ptet-LuxR-Ptrc-RFP on pSB6A1 to E. coli as “3OC12HSL dependent CmR and C4HSL producer cell”.
In this E. coli, constitutively expressed LuxR activates the expression of CmR and RhlI in the presence of 3OC12HSL.

To confirm 3OC12HSL-dependent CmR production, we cultured Plux-CmR-RhlI cell in LB media with Amp, Kan and Cm.
Fig.1 shows OD590 by CmR producer cells dependent on different conditions.

Fig. 1. 3OC12HSL-dependent CmR expressionh in 100 microg / mL chloramphenicol

To confirm 3OC12HSL-dependent C4HSL production, we introduced Ptet-RhlR on pSB6A1 and Plux-GFP on pSB3K3 to E. coli as “Rhl reporter cell”.
Fig.2 shows fluorescence intensity by Rhl reporter cells dependent on different conditions.

Fig. 2. C4HSL production in the presence of 3OC12HSL

From these experiments, we confirmed that the part Plux-CmR-RhlI (BBa_K1529797) worked accurately.

Moreover, by co-culturing the cells containing this part with the cells containing C4HSL dependent 3OC12HSL producer part, Prhl(RL)-CmR-LasI(BBa_K1529302), we succeeded in constructing a positive feedback system.(Fig. 3.)

Fig. 3. The growth of Customer(Plux-CmR-RhlI) and Campany(Prhl(RL)-CmR-RhlI) when co-cultured for 6 hours.

For more information, see [http://2014.igem.org/Team:Tokyo_Tech/Project our work in Tokyo_Tech 2014 wiki].

Sequence and Features