Composite

Part:BBa_K1321325

Designed by: Michael Florea   Group: iGEM14_Imperial   (2014-10-08)
Revision as of 23:44, 20 October 2014 by Mf1512 (Talk | contribs)

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 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


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal prefix found in sequence at 4802
    Illegal SpeI site found at 1063
    Illegal PstI site found at 1946
  • 12
    INCOMPATIBLE 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
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 4802
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal prefix found in sequence at 4802
    Illegal SpeI site found at 1063
    Illegal PstI site found at 1946
  • 25
    INCOMPATIBLE 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
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1004


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