Difference between revisions of "Part:BBa I739003"
Stefan Luzi (Talk | contribs) (→Purpose) |
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===Purpose=== | ===Purpose=== | ||
− | <p>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. When complexed with HSL, the constitutively synthesized LuxR interacts with the double promoters [https://parts.igem.org/wiki/index.php/Part: | + | <p>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. When complexed with HSL, the constitutively synthesized LuxR interacts with the double promoters [https://parts.igem.org/wiki/index.php/Part:BBa_I739104 BBa_I739104] and [https://parts.igem.org/wiki/index.php/Part:BBa_I739105 BBa_I739105] which are parts of composites [https://parts.igem.org/wiki/index.php/Part:BBa_I739006 BBa_I739006] and [https://parts.igem.org/wiki/index.php/Part:BBa_I739007 BBa_I739007] respectively.</p> |
===Testing=== | ===Testing=== |
Revision as of 12:50, 19 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. When complexed with HSL, the constitutively synthesized LuxR interacts with the double promoters BBa_I739104 and BBa_I739105 which are parts of composites BBa_I739006 and BBa_I739007 respectively.
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]