Regulatory

Part:BBa_K1677300:Experience

Designed by: Isabelle Capell-Hattam   Group: iGEM15_BABS_UNSW_Australia   (2015-08-23)

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Applications of BBa_K1677300


A LacZ assay was carried out with p170, CP44 and ASR fused to a promoter activity reporter (BBa_I732095) in E. Coli and grown in LB with antibiotics for 8 hours. The data normalized to OD600 of the cultures reveals a decrease in lacZ production correlated with a decrease in pH for the CP44 promoter. A slight increase was observed in both p170 and ASR with the decline in pH, however expression of lacZ is much lower even at neutral pH than with CP44.


When the above data is normalized to the neutral pH value of the culture the differential expression at varying pH values becomes more pronounced. Both the E. Coli and L. Lactis ASR promoters show an increase in activity at lower pH values.
Overall this suggests that our biobricked p170 works as predicted by Madsen et al. (1999) and that it will up-regulate transcription at lower pH values.
Notably this is a significant result as the assay was carried out in E. Coli, not L. Lactis, where the promoter was initially characterized.

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