Difference between revisions of "Part:BBa K3962353: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 a suitable promoter for regulating antitoxin genes because pBAD can induce very high levels of RelE expression to neutralize toxic effects of RelB. We optimized the codon for the expression of the gene in E. coli.  
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pBAD has been intensively investigated by previous iGEM projects and has tight regulation upon downstream genes. It is a suitable promoter for regulating antitoxin genes because pBAD can induce very high levels of RelE expression to neutralize toxic effects of RelB. Codon optimization was performed for the expression of the gene in E. coli.  
  
  

Latest revision as of 08:09, 16 October 2021


Inducible expression of antitoxin RelB by pBAD


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
    Illegal XhoI site found at 1339
  • 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 by previous iGEM projects and has tight regulation upon downstream genes. It is a suitable promoter for regulating antitoxin genes because pBAD can induce very high levels of RelE expression to neutralize toxic effects of RelB. Codon optimization was performed for the expression of the gene in E. coli.


Source

All sequences of subparts are from iGEM registry.


References