Part:BBa_K1321325
pLux02
This is the red chromoprotein eforRed (BBa_K1073022) in pSEVA331-Bb plasmid backbone (part BBa_K1321300). This construct is a member of the G.xylinus genetic engineering toolbox.
G.xylinus toolbox was designed to ease genetic engineering of cellulose-based biomaterials using the cellulose synthesizing bacterium Gluconacetobacter xylinus (parts Bba_K1321305 and BBa_K1321306) by characterizing and providing a collection of widely used parts in pSEVA331-Bb backbone. 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 as 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 toolbox 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 toolbox available for the synthetic biology community, Imperial iGEM 2014 team has made the toolbox freely available upon request, with quality control provided (see Experience). For requests, please contact Imperial iGEM 2014 team.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal prefix found in sequence at 4802
Illegal SpeI site found at 1063
Illegal PstI site found at 1946 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 4802
Illegal SpeI site found at 1063
Illegal PstI site found at 1946
Illegal NotI site found at 1939
Illegal NotI site found at 4808 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 4802
- 23INCOMPATIBLE WITH RFC[23]Illegal prefix found in sequence at 4802
Illegal SpeI site found at 1063
Illegal PstI site found at 1946 - 25INCOMPATIBLE WITH RFC[25]Illegal prefix found in sequence at 4802
Illegal XbaI site found at 4817
Illegal SpeI site found at 1063
Illegal PstI site found at 1946
Illegal NgoMIV site found at 3121
Illegal AgeI site found at 1642
Illegal AgeI site found at 1754 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1004
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