Difference between revisions of "Part:BBa K193001"

 
 
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<partinfo>BBa_K193001 short</partinfo>
 
<partinfo>BBa_K193001 short</partinfo>
  
A cI repressible promoter driving production  LuxI enzyme
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CI repressible LuxI enzyme generator.
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This part is used to transform E.coli strain which expresses CI represser.
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We improved existing BioBrick Part [https://parts.igem.org/Part:BBa_F1610 BBa_F1610], and constructed K193001.
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[[Image:tokyo_tech_consortium11.png|the vertical line is fluorescence intensity (a.u.)]]
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luxR(AHL+),luxR(AHL-) ; strain N4830 transformed only with luxR expressing plasmid(BBa_J54140)
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luxR+luxI; strain N4830 transformed with luxR expressing plasmid and luxI expressing plasmid
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luxI; strain N4830 transformed with luxI expressing plasmid
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More detail information, http://2009.igem.org/Team:Tokyo_Tech/Consortium.
  
which produces an AHL (3OC6HSL).
 
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 04:08, 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

More detail information, http://2009.igem.org/Team:Tokyo_Tech/Consortium.


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]