Difference between revisions of "Part:BBa I739003"
Stefan Luzi (Talk | contribs) (→Testing) |
Stefan Luzi (Talk | contribs) (→Testing) |
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===Testing=== | ===Testing=== | ||
− | + | Checked for uniqueness of restriction enzyme cleavage sites:<br> | |
Eco: ok<br> | Eco: ok<br> | ||
Xba: ok<br> | Xba: ok<br> | ||
Spe: ok<br> | Spe: ok<br> | ||
− | Pst: ok<br> | + | Pst: ok<br> |
+ | |||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 13:19, 11 October 2007
Constitutive expression cassette for LuxR (J23100.B0034.C0062.B0015)
Part Structure
The Biobrick encodes luxR (BBa_C0062) under control of the constitutive promoter BBa_J23100 followed by the ribosome binding site BBa_B0034. The transcription of luxR is terminated by the double terminator BBa_B0015.
Mode of Action
Two molecules of LuxR protein form a complex with two molecules of the signalling compound homoserine lactone (HSL) (e.g. AHL). This complex binds to a palindromic site on the promoter BBa_R0062, increasing the rate of transcription. So far, this LuxI/R system is the best characterized system of all cell-cell signaling systems.
Purpose
This Biobrick was designed for the [http://parts.mit.edu/igem07/index.php/ETHZ ETHZ iGEM 2007 project] and belongs to the constitutive part of the system. In the project description, this part is also termed Part 3. The constitutively synthesized luxR interacts with .... when complexed with HSL.
Testing
Checked for uniqueness of restriction enzyme cleavage sites:
Eco: ok
Xba: ok
Spe: ok
Pst: ok
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]