Difference between revisions of "Part:BBa K3962343:Design"

 
 
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===Design Notes===
 
===Design Notes===
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pBAD has been intensively investigated and has tight regulation upon downstream genes. It is the most suitable promoter for regulating toxin genes and preventing their toxic effects. For RelE, it has also been used as a part of a kill switch.  
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pBAD has been intensively investigated and has tight regulation upon downstream genes. It is the most suitable promoter for regulating toxin genes and preventing their toxic effects because glucose can be used to repress its activity. Codon optimization was performed for the expression of the gene in E. coli.  
  
  

Latest revision as of 07:54, 16 October 2021


arabinose-mediated inducible expression of toxin RelE


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1205
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 1144
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 979
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 961


Design Notes

pBAD has been intensively investigated and has tight regulation upon downstream genes. It is the most suitable promoter for regulating toxin genes and preventing their toxic effects because glucose can be used to repress its activity. Codon optimization was performed for the expression of the gene in E. coli.



Source

All parts come from the iGEM registry.


References