Part:BBa_K1321331
araC-Pbad in pSEVA331-Bb
This is araC-Pbad - Arabinose inducible regulatory promoter/repressor unit in pSEVA331-Bb plasmid backbone (part BBa_K1321300). This construct is a member of the G.xylinus genetic engineering toolkit (parts BBa_K1321295 - BBa_K1321332).
G.xylinus toolkit was designed to ease genetic engineering of cellulose-based biomaterials using the cellulose synthesizing bacterium Gluconacetobacter xylinus (parts Bba_K1321305 and BBa_K1321306). As no registry parts had been tested in G.xylinus, the aim of this toolkit was to determine the parts usable in G.xylinus and to characterize them in this host. pSEVA331-Bb is a non-standard broad host range plasmid capable of replication in G.xylinus and E.coli (a shuttle vector) and was selected because the registry's standard plasmid backbone pSB1C3 can not be used for G.xylinus engineering.
NOTE: Because the registry's standard plasmid backbone pSB1C3 is not capable of replication in Gluconacetobacter species, the G.xylinus genetic engineering toolkit is housed mainly in pSEVA331-Bb. pSEVA331-Bb is a non-standard backbone, which therefore can't be quality controlled by and maintained in the Registry. However, in order to make the G.xylinus toolkit available for the synthetic biology community, Imperial iGEM 2014 team has made it freely available upon request, with quality control provided (see Experience). To request, please contact Imperial iGEM 2014 team.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal prefix found in sequence at 4089
Illegal suffix found in sequence at 1218 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 4089
Illegal SpeI site found at 1219
Illegal PstI site found at 1233
Illegal NotI site found at 1226
Illegal NotI site found at 4095 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 4089
Illegal BamHI site found at 1144 - 23INCOMPATIBLE WITH RFC[23]Illegal prefix found in sequence at 4089
Illegal suffix found in sequence at 1219 - 25INCOMPATIBLE WITH RFC[25]Illegal prefix found in sequence at 4089
Illegal XbaI site found at 4104
Illegal SpeI site found at 1219
Illegal PstI site found at 1233
Illegal NgoMIV site found at 2408
Illegal AgeI site found at 979 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 961
None |