Difference between revisions of "Part:BBa K193001"

Line 8: Line 8:
 
We improved existing BioBrick Part [https://parts.igem.org/Part:BBa_F1610 BBa_F1610], and constructed K193001.
 
We improved existing BioBrick Part [https://parts.igem.org/Part:BBa_F1610 BBa_F1610], and constructed K193001.
  
[[Image:tokyo_tech_consortium11.png]]
+
[[Image:tokyo_tech_consortium11.png|the vertical line is fluorescence intensity (a.u.)]]
 +
 
 +
luxR(AHL+),luxR(AHL-) ; strain N4830 transformed only with luxR expressing plasmid(BBa_J54140)
 +
 
 +
luxR+luxI; strain N4830 transformed with luxR expressing plasmid and luxI expressing plasmid
 +
 
 +
luxI; strain N4830 transformed with luxI expressing plasmid
 +
 
  
  

Revision as of 04:04, 22 October 2009

CI repressible LuxI enzyme generator

CI repressible LuxI enzyme generator.

This part is used to transform E.coli strain which expresses CI represser.

We improved existing BioBrick Part BBa_F1610, and constructed K193001.

the vertical line is fluorescence intensity (a.u.)

luxR(AHL+),luxR(AHL-) ; strain N4830 transformed only with luxR expressing plasmid(BBa_J54140)

luxR+luxI; strain N4830 transformed with luxR expressing plasmid and luxI expressing plasmid

luxI; strain N4830 transformed with luxI expressing plasmid


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 712
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]