Difference between revisions of "Part:BBa K649105"
Line 3: Line 3:
 
      
 
      
  
−
[[Image:Lsrr.png|thumb|center|500px|Fluorescence intensity is decreased by LsrR repression.<br>This work is done by Hiroki Yoshise.]]
+
[[Image:20111028133941%21LsrR_repression1.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, <i>lsrK</i> has mutation and does not work properly and oher genes work correctly.
 
As we described in [https://parts.igem.org/Part:BBa_K649101 BBa_K649101], in this part, <i>lsrK</i> has mutation and does not work properly and oher genes work correctly.

Revision as of 14:23, 28 October 2011

PlsrA-gfp-PlsrR-lsrR


Fluorescence intensity is decreased by LsrR repression.
This work is done by Hiroki Yoshise.

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 lsrA promoter. 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


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 2579
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 2253
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 770