Regulatory
cI+luxR
Part:BBa_R0065
Designed by: Vinay S Mahajan, Voichita D. Marinescu, Brian Chow, Alexander D Wissner-Gross and Peter Carr Group: Antiquity (2003-01-31)
Revision as of 18:18, 6 November 2010 by Supacalafrglstic (Talk | contribs)
Promoter (lambda cI and luxR regulated -- hybrid)
cI repressor negatively regulates this promoter and LuxR activates its transcription.The effect of cI is dominant over LuxR. This part is based on the LuxR and cI repressor regulated hybrid promoter designed and tested by Ron Weiss. It requires the binding of two cI repressor dimers for maximal repression and contains two cI repressor binding sites namely, OR1 and OR2. This promoter is leaky in the sense that 'some' transcription is seen in the absence of both cI and LuxR.
LuxI | cI | activity of promoter |
+ | + | zero |
+ | - | maximum |
- | + | zero |
- | - | leaky (no quantitative information) |
Usage and Biology
Pretty good 'off' in the absence of LuxR/HSL. [jb, 5/24/04]
- very leaky (no LuxR/HSL) at high (100-300) copy number. can only be slightly induced by LuxR+3OC6HSL. (jt, ut-austin; 08/11/05)
- Part has since been improved by the [http://2010.igem.org/Team:MIT 2010 MIT iGEM] team in the form of the part Part:BBa_K415032 where the second -10 promoter region has been removed, and the part is thus less leaky.
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/positive
//regulation/negative
//regulation/multiple
//classic/regulatory/uncategorized
//direction/forward
//chassis/prokaryote/ecoli
//promoter
//regulation/positive
//regulation/negative
//regulation/multiple
//classic/regulatory/uncategorized
negative_regulators | 1 |
positive_regulators | 1 |