Difference between revisions of "Part:BBa K2151005"

 
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<partinfo>BBa_K2151005 short</partinfo>
 
<partinfo>BBa_K2151005 short</partinfo>
  
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<p>This part consists of E5501 (GFP with medium ribosome binding site) under the control of p32, a strong constitutive bacterial promoter. Its intended use is to serve as a promoter-reporter construct in lactic acid bacteria. p32 is used as a promoter in expression vectors functioning within <i>Streptococcus thermophilus</i> </p>
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<p>We used p32 as a candidate promoter to drive gene expression in both <i>Streptococcus thermophilus</i> and <i>E. coli</i>. Quantification of p32 using GFP revealed promoter strength on par with strong Anderson promoters (81% as strong as J23100, 115% as strong as J23101).</p></p>
  
 
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Revision as of 21:36, 8 October 2016


p32-E5501: GFP under control of strong constitutive promoter

This part consists of E5501 (GFP with medium ribosome binding site) under the control of p32, a strong constitutive bacterial promoter. Its intended use is to serve as a promoter-reporter construct in lactic acid bacteria. p32 is used as a promoter in expression vectors functioning within Streptococcus thermophilus

We used p32 as a candidate promoter to drive gene expression in both Streptococcus thermophilus and E. coli. Quantification of p32 using GFP revealed promoter strength on par with strong Anderson promoters (81% as strong as J23100, 115% as strong as J23101).

</p>

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 721