Coding

Part:BBa_K2255001:Design

Designed by: Jeremy Cartalas   Group: iGEM17_Aix-Marseille   (2017-08-28)
Revision as of 02:43, 2 November 2017 by Kamy (Talk | contribs) (→‎Design Notes)

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RBS + Acyl-CoA isomerase


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 SapI site found at 571


Design Notes

This Acyl-CoA isomerase[1] is necessary to the production of 2-cis-decenenoic acid by Pseudomonas aeruginosa, so we search its DNA sequence in the genome to create our first biobrick. This enzyme gene is on a operon along the other gene crucial for the formation of 2-cis-decenenoic acid.

We took the gene coding for the right enzyme and optimized its sequence for a production in E.coli. Then, a ribosome binding site (RBS) was added to the sequence in order to make an operon with BBa_K2255000 and BBa_K2255002. Finaly, a Rfc10 prefix and sufix was added.

Source

It came from the genomic sequence of Pseudomonas aeruginosa.

References

  1. ↑ Amari, D. T., Marques, C. N. H. & Davies, D. G. The Putative Enoyl-Coenzyme A Hydratase DspI Is Required for Production of the Pseudomonas aeruginosa Biofilm Dispersion Autoinducer cis-2-Decenoic Acid. J. Bacteriol. 195, 4600–4610 (2013).