Difference between revisions of "Part:BBa K2151003"
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− | . | + | <p>This part consists of E5501 (GFP with medium ribosome binding site) under the control of pHLBA, a strong constitutive bacerial promoter. Its intended use is to serve a promoter-reporter construct in lactic acid bacteria. pHLBA was initially identified in studies of <i>Lactobacillus bulgaricus</i> where it drives the expression of histone-like proteins. pHLBA is likely functional in all lactic acid bacteria. </p> |
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+ | <p>We used pHLBA as a candidate promoter to drive gene expression in both <i>Streptococcus thermophilus</i> and <i>E. coli</i>. Quantification of pHLBA using GFP in <i>E. coli</i> revealed promoter strength on par with strong Anderson promoters (93% as strong as J23100, 132% as strong as J23101).</p> | ||
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Revision as of 21:24, 8 October 2016
pHLBA-E5501: GFP under control of strong constitutive promoter
This part consists of E5501 (GFP with medium ribosome binding site) under the control of pHLBA, a strong constitutive bacerial promoter. Its intended use is to serve a promoter-reporter construct in lactic acid bacteria. pHLBA was initially identified in studies of Lactobacillus bulgaricus where it drives the expression of histone-like proteins. pHLBA is likely functional in all lactic acid bacteria.
We used pHLBA as a candidate promoter to drive gene expression in both Streptococcus thermophilus and E. coli. Quantification of pHLBA using GFP in E. coli revealed promoter strength on par with strong Anderson promoters (93% as strong as J23100, 132% as strong as J23101).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 707