Difference between revisions of "Part:BBa K4260031"

 
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This is a bidirectional promoter region that helps the transcription of two different genes, one in the leader chain of DNA and other in the antisense chain. This type of arrangement is commonly found in operons, in bacteria. This part promotes the transcription of IemR, a trancriptional activator, and together both parts promote the transcription of the coding gene of isoeugenol monooxygenase.  
 
This is a bidirectional promoter region that helps the transcription of two different genes, one in the leader chain of DNA and other in the antisense chain. This type of arrangement is commonly found in operons, in bacteria. This part promotes the transcription of IemR, a trancriptional activator, and together both parts promote the transcription of the coding gene of isoeugenol monooxygenase.  
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<center>
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          <img
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              src="https://parts.igem.org/File:Promotor_pseudomonas.jpeg"
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              alt="Fig1-sp"
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              width="700"
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              align="center"
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            />
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            </center>
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<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 02:26, 14 October 2022


Promoter, for Iem & Iso

This is a bidirectional promoter region that helps the transcription of two different genes, one in the leader chain of DNA and other in the antisense chain. This type of arrangement is commonly found in operons, in bacteria. This part promotes the transcription of IemR, a trancriptional activator, and together both parts promote the transcription of the coding gene of isoeugenol monooxygenase.

         <img
             src="https://parts.igem.org/File:Promotor_pseudomonas.jpeg"
             alt="Fig1-sp"
             width="700"
             align="center"
           />


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 164