Coding
Biosurfact

Part:BBa_K653000:Design

Designed by: Team Panama 2011   Group: iGEM11_Panama   (2011-09-26)
Revision as of 03:10, 27 September 2011 by Ernestopro (Talk | contribs) (→‎Source)

Re-designing "The Biosurfactator" The first Central American BioBrick


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 103
    Illegal BamHI site found at 663
    Illegal XhoI site found at 839
    Illegal XhoI site found at 2125
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 1018
    Illegal NgoMIV site found at 1739
    Illegal NgoMIV site found at 1852
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 328
    Illegal BsaI site found at 1368
    Illegal BsaI.rc site found at 512


Design Notes

The RhlAB gene complex has shown illegal restriction sites according to the assembly standard protocol 10. We faced this problem by applying the mutagenesis protocol that consist in doing silent mutations that change the nucleotides of our rhlAB gene that are cut by the Pstl restriction enzyme. This will give us a standardized coding sequence of the rhlAB gene compatible with the Assembly Standard protocol 10 and a new BioBrick part for the Registry.



Source

Pseudomonas aeruginosa from INDICASAT lab. and the genomic sequence of RhlAB was reviwed in genBank (ID 878955 for rhamnosyltransferase A and ID 878954 for rhamnosyltransferase B) http://www.indicasat.org.pa/ http://www.ncbi.nlm.nih.gov/gene?term=RhlA%20ID%20878955 http://www.ncbi.nlm.nih.gov/gene?term=RhlB%20ID%20878954

References