Difference between revisions of "Part:BBa K649105"
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[[Image:Lsrr.png|thumb|center|500px|Fluorescence intensity is decreased by LsrR repression.<br>This work is done by Hiroki Yoshise.]] | [[Image:Lsrr.png|thumb|center|500px|Fluorescence intensity is decreased by LsrR repression.<br>This work is done by Hiroki Yoshise.]] | ||
− | + | As we described in [https://parts.igem.org/Part:BBa_K649101 BBa_K649101], in this part, lsrK has mutation and does not work properly and oher genes work correctly. | |
We confirmed that LsrR represses lsrA promoter. We measured LsrR repression activity by using a plasmid (BBa_K649105) which have a lsrR gene downstream of lsrA promoter-gfp.By the LsrR repression, the fluorescence intensity decreased 3-fold. This result shows that LsrR successfully repressed promoter lsrA. The working part we created allow the use of AI-2 as a signaling molecule, which is a very powerful tool to build complex Synthetic Biology systems. | We confirmed that LsrR represses lsrA promoter. We measured LsrR repression activity by using a plasmid (BBa_K649105) which have a lsrR gene downstream of lsrA promoter-gfp.By the LsrR repression, the fluorescence intensity decreased 3-fold. This result shows that LsrR successfully repressed promoter lsrA. The working part we created allow the use of AI-2 as a signaling molecule, which is a very powerful tool to build complex Synthetic Biology systems. |
Revision as of 00:48, 5 October 2011
PlsrA-gfp-PlsrR-lsrR
As we described in BBa_K649101, in this part, lsrK has mutation and does not work properly and oher genes work correctly.
We confirmed that LsrR represses lsrA promoter. We measured LsrR repression activity by using a plasmid (BBa_K649105) which have a lsrR gene downstream of lsrA promoter-gfp.By the LsrR repression, the fluorescence intensity decreased 3-fold. This result shows that LsrR successfully repressed promoter lsrA. The working part we created allow the use of AI-2 as a signaling molecule, which is a very powerful tool to build complex Synthetic Biology systems.
For more information, see [http://2011.igem.org/Team:Tokyo_Tech/Projects/RPS-game/assay#6. our work in Tokyo_Tech 2011 wiki].
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 2579
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 2253
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 770