Difference between revisions of "Part:BBa K1541017"
Line 9: | Line 9: | ||
====RBS Engineering==== | ====RBS Engineering==== | ||
− | The [[Ribosome_Binding_Site|ribosomal binding site (RBS)]] | + | The [[Ribosome_Binding_Site|ribosomal binding site (RBS)]] is a sequence on the mRNA crucial for the translation initiation step in prokaryotes. |
+ | |||
<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K1541017 SequenceAndFeatures</partinfo> | <partinfo>BBa_K1541017 SequenceAndFeatures</partinfo> |
Revision as of 23:02, 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.
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]