Regulatory
pRecA
Part:BBa_K093000
Designed by: Julian Wiegelmann, Danielle Nash Group: iGEM08_Waterloo (2008-10-26)
pRecA with LexA binding site
This is a pRecA promoter with LexA binding sites. LexA is cleaved by RecA when RecA is upregulated due to induction of the SOS response triggered by single stranded DNA. For this part to work it must be in a RecA+ strain of E. coli such as TG1.
Preliminary testing has been done to characterize this promoter using RFP as a reporter (K093009). The promoter is active, demonstrating minimal leaky expression compared to the constitutive promoter pconst (J23118). The ability to upregulate has been tested by exposing culture to UV to induce crosslinking, but more trials must be conducted to optimize conditions. A crosslinking agent such as mitomycin C could also be used to test induction.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
[edit]
Categories
Parameters
//rnap/prokaryote/ecoli/sigma70
//direction/forward
//chassis/prokaryote/ecoli
//promoter
//regulation/negative
//direction/forward
//chassis/prokaryote/ecoli
//promoter
//regulation/negative
negative_regulators | 1 |
positive_regulators |