Generator
Part:BBa_I737021:Design
Designed by: Vladislav Lavrovsky Group: iGEM07_Calgary (2007-10-26)
Constitutively expressed Agarase part.
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1943
Illegal PstI site found at 366 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1943
Illegal NheI site found at 188
Illegal NheI site found at 983
Illegal PstI site found at 366 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1943
Illegal XhoI site found at 2046 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1943
Illegal PstI site found at 366 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1943
Illegal PstI site found at 366
Illegal AgeI site found at 450 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1401
Illegal SapI.rc site found at 1799
Illegal SapI.rc site found at 1877
Design Notes
There are EcorI and PstI sites. This limits construction. Future versions will be mutated by site-directed mutagenesis. The flanks of the gene were included for the signal peptide. Agarase is exported in the source organism using the TAT export system with e. coli K12 has, unfortunately so far e. coli dont degrade agar when transformed with this part. We are not sure whether it is a problem with expression or export.
Source
Cloned from Pseudoalteromonas atlantica T6C.