Difference between revisions of "Part:BBa K396000"

 
 
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===Usage and Biology===
 
===Usage and Biology===
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T7/CI-OR1 hybrid promoter was designed to be activated by T7 RNA Polymerase and repressed by lambda CI protein. In sequence design,  lambda CI operator site 1 (OR1, Part of BBa_R1051) was directly attached to the downstream of T7 promoter sequence (BBa_I719005). This characterization was implemented to validate the promoter function. In results, the activation and repression was actually observed.
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<html><center><img src="https://static.igem.org/mediawiki/2010/1/10/T7-CI-1.png" width="600px"><br>
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<img src="https://static.igem.org/mediawiki/2010/b/bd/CI-2.png" width="600px"></center></html>
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Under the situation of CI non-expressed , T7 RNAP causes GFP expression by activating T7/CI hybrid
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promoter (Fig.1). On the other hand, under the situation of CI expressed, T7 RNAP does not cause GFP
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expression (Fig.2). The reason of this is considered as following.  Under the situation of CI expressed,
 +
even though T7 RNAP tries to  activate T7/CI promoter, the promoter Is repressed by CI because the
 +
ability of CI repression is superior to the one of T7 activation for this promoter.  So it is concluded that
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T7/CI hybrid  promoter is to be activated by T7 RNA Polymerase and repressed by lambda  CI protein,following the rules of CI repression > T7 activation.   
 +
 +
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====Reference====
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Dubendorf, J.W. & Studier, F.W. Controlling basal expression in an
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inducible T7 expression system by blocking the target T7 promoter with
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lac repressor. Journal of Molecular Biology 219, 45-59 (1991).
 +
 +
 +
  
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
 
<partinfo>BBa_K396000 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K396000 SequenceAndFeatures</partinfo>

Latest revision as of 14:23, 5 November 2010

T7/CI Hybrid Promoter with GFP (composite with LuxR generator)

T7/CI hybrid promoter is the hybrid promoter which is activated by T7 RNA Polymerase and regulated by lambda CI protein.


Usage and Biology

T7/CI-OR1 hybrid promoter was designed to be activated by T7 RNA Polymerase and repressed by lambda CI protein. In sequence design, lambda CI operator site 1 (OR1, Part of BBa_R1051) was directly attached to the downstream of T7 promoter sequence (BBa_I719005). This characterization was implemented to validate the promoter function. In results, the activation and repression was actually observed.


Under the situation of CI non-expressed , T7 RNAP causes GFP expression by activating T7/CI hybrid promoter (Fig.1). On the other hand, under the situation of CI expressed, T7 RNAP does not cause GFP expression (Fig.2). The reason of this is considered as following. Under the situation of CI expressed, even though T7 RNAP tries to activate T7/CI promoter, the promoter Is repressed by CI because the ability of CI repression is superior to the one of T7 activation for this promoter. So it is concluded that T7/CI hybrid promoter is to be activated by T7 RNA Polymerase and repressed by lambda CI protein,following the rules of CI repression > T7 activation.


Reference

Dubendorf, J.W. & Studier, F.W. Controlling basal expression in an inducible T7 expression system by blocking the target T7 promoter with lac repressor. Journal of Molecular Biology 219, 45-59 (1991).



Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 783
    Illegal NheI site found at 806
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 852
    Illegal BamHI site found at 1421
    Illegal XhoI site found at 822
    Illegal XhoI site found at 1322
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]