Difference between revisions of "Part:BBa K819008"

 
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<partinfo>BBa_K819008 short</partinfo>
 
<partinfo>BBa_K819008 short</partinfo>
  
luxABCDE gene ligated to the rear of T7 promoter. When transformed into BL21(DE3) E.coli strain, add different amount IPTG to reach different final concentration of IPTG in the medium can induce different level of Lux ligt emission. No substrate is needed.
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Lux operon genes (from [https://parts.igem.org/Part:BBa_K325909:Design BBa_K325909]) and related RBS are placed under T7 promoter. Cells transformed with this part can produce blue luminescence while no exogenous substrate is needed.<br/><br/>luxbrick under T7 promoter is very modular, because it is transcribed by T7 polymerase, which can be placed under any other promoter, forming a interface between luxbrick and other systems.Also, when transformed into BL21 cells, it can be induced with IPTG to reach a high expression level.
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Revision as of 08:43, 25 September 2012

Lux Operon under T7 promoter

Lux operon genes (from BBa_K325909) and related RBS are placed under T7 promoter. Cells transformed with this part can produce blue luminescence while no exogenous substrate is needed.

luxbrick under T7 promoter is very modular, because it is transcribed by T7 polymerase, which can be placed under any other promoter, forming a interface between luxbrick and other systems.Also, when transformed into BL21 cells, it can be induced with IPTG to reach a high expression level.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 3014
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 2012
    Illegal XhoI site found at 2842
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 4401
    Illegal BsaI.rc site found at 1410
    Illegal SapI.rc site found at 4726