Difference between revisions of "Part:BBa K3606018"

 
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<partinfo>BBa_K3606018 short</partinfo>
 
<partinfo>BBa_K3606018 short</partinfo>
  
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<h2>Usage and Biology:</h2>
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This promoter comes from a kit which contains combinations of specific constitutive bacterial promoters that vary in strength.
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<h2>Design:</h2>
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We have chosen a series of constitutive promoters with different strength which include P9. They are used to reliably drive expression of CaAP and McbABCEFG in E. coli in a controlled, reliable manner. We have tested these different, unique combinations to find the best expression level of CaAP and McbABCEFG.
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<h2> Characterization:</h2>
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<h2>Further Application:</h2>
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This part comes from a collection of precisely quantitated bacterial transcription and translation initiation elements. You can directly choose a promoter with suitable strength to drive expression of a gene of interest in E. coli from those we have tested. You can also combine them with other elements to achieve your goal.
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<h2>References:</h2>
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[1] Mutalik VK, Guimaraes JC, Cambray G, Lam C, Christoffersen MJ, Mai QA, Tran AB, Paull M, Keasling JD, Arkin AP, Endy D. Precise and reliable gene expression via standard transcription and translation initiation elements. Nat Methods. 2013 Apr;10(4):354-60. doi: 10.1038/nmeth.2404. Epub 2013 Mar 10. PMID: 23474465.
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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 06:19, 25 October 2020


P9 promoter

Usage and Biology:

This promoter comes from a kit which contains combinations of specific constitutive bacterial promoters that vary in strength.

Design:

We have chosen a series of constitutive promoters with different strength which include P9. They are used to reliably drive expression of CaAP and McbABCEFG in E. coli in a controlled, reliable manner. We have tested these different, unique combinations to find the best expression level of CaAP and McbABCEFG.

Characterization:


Further Application:

This part comes from a collection of precisely quantitated bacterial transcription and translation initiation elements. You can directly choose a promoter with suitable strength to drive expression of a gene of interest in E. coli from those we have tested. You can also combine them with other elements to achieve your goal.

References:

[1] Mutalik VK, Guimaraes JC, Cambray G, Lam C, Christoffersen MJ, Mai QA, Tran AB, Paull M, Keasling JD, Arkin AP, Endy D. Precise and reliable gene expression via standard transcription and translation initiation elements. Nat Methods. 2013 Apr;10(4):354-60. doi: 10.1038/nmeth.2404. Epub 2013 Mar 10. PMID: 23474465.


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
    COMPATIBLE WITH RFC[1000]