Part:BBa_K653000:Design
Re-designing "The Biosurfactator" The first Central American BioBrick
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE 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 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1018
Illegal NgoMIV site found at 1739
Illegal NgoMIV site found at 1852 - 1000INCOMPATIBLE 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.ncbi.nlm.nih.gov/gene?term=RhlA%20ID%20878955
http://www.ncbi.nlm.nih.gov/gene?term=RhlB%20ID%20878954
http://www.indicasat.org.pa/