Part:BBa_K1321321

Anderson J23118-RFP in pSEVA331-Bb

This is Anderson promoter J23118 driving the expression of Elowitz RBS-mFRP in pSEVA331-Bb plasmid backbone (part BBa_K1321300) and 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 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 can't be quality controlled and thus maintained by 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

Assembly Compatibility:

• 10
  INCOMPATIBLE WITH RFC[10]

  Illegal prefix found in sequence at 3776
  Illegal SpeI site found at 37
  Illegal PstI site found at 920
  
• 12
  INCOMPATIBLE WITH RFC[12]

  Illegal EcoRI site found at 3776
  Illegal NheI site found at 7
  Illegal NheI site found at 30
  Illegal SpeI site found at 37
  Illegal PstI site found at 920
  Illegal NotI site found at 913
  Illegal NotI site found at 3782
  
• 21
  INCOMPATIBLE WITH RFC[21]

  Illegal EcoRI site found at 3776
  
• 23
  INCOMPATIBLE WITH RFC[23]

  Illegal prefix found in sequence at 3776
  Illegal SpeI site found at 37
  Illegal PstI site found at 920
  
• 25
  INCOMPATIBLE WITH RFC[25]

  Illegal prefix found in sequence at 3776
  Illegal XbaI site found at 3791
  Illegal SpeI site found at 37
  Illegal PstI site found at 920
  Illegal NgoMIV site found at 2095
  Illegal AgeI site found at 616
  Illegal AgeI site found at 728
  
• 1000
  COMPATIBLE WITH RFC[1000]