Difference between revisions of "Part:BBa K1541017"
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====RBS Engineering==== | ====RBS Engineering==== | ||
− | The [[Ribosome_Binding_Site|ribosomal binding site (RBS)]] is a sequence on the mRNA crucial for the translation initiation step in prokaryotes. | + | The [[Ribosome_Binding_Site|ribosomal binding site (RBS)]] is a sequence on the mRNA crucial for the translation initiation step in prokaryotes, which highly influences protein levels. The influence of the RBS sequence also depend of the genetic context and identical RBSsequences in different contexts can result in different protein expression levels[1]. |
<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> |
Revision as of 23:08, 16 October 2014
rhlI with optimized RBS
This part contains the part C0170 (RhlI), which is an autoinducer synthesis protein that produces N-butyryl-L-HSL (C4-HSL) which binds to RhlR (C0171), obtained from Pseudomonas aeruginosa. Since this part was used in a low-copy vector, RBS engineering was performed to increase expression levels of this enzyme and thus also improve the production of C4-HSL.
Usage and Biology
Quorum Sensing
RhlI is the autoinducer synthetase from Pseudomonas aeruginosa, which can synthesize the molecule N-butyryl-L-HSL (C4-HSL). C4-HSL can bind to the regulatory protein RhlR (C0171). Once C4-HSL is bound to RhlR it can activate the promoters R0071 or I14017.
RBS Engineering
The ribosomal binding site (RBS) is a sequence on the mRNA crucial for the translation initiation step in prokaryotes, which highly influences protein levels. The influence of the RBS sequence also depend of the genetic context and identical RBSsequences in different contexts can result in different protein expression levels[1].
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]