Difference between revisions of "Part:BBa K1321325"

Latest revision as of 15:48, 6 May 2016

pLux02

This plasmid encodes for LuxR generator and mRFP1 behind pLux promoter, making mRFP1 inducible via AHL, in pSEVA331Bb backbone. See attached file for annotated sequence. This construct is a member of the Komagataeibacter genetic engineering toolkit (parts BBa_K1321295 - BBa_K1321332). File:IC14 pLux02.gb

Komagataeibacter toolkit was designed to ease genetic engineering of cellulose-based biomaterials using the cellulose synthesizing bacterium Komagataeibacter rhaeticus iGEM (parts Bba_K1321305 and BBa_K1321306). As no registry parts had been tested in K. rhaeticus, the aim of this toolkit was to determine the parts usable in K. rhaeticus and to characterize them in this host. pSEVA331-Bb is a non-standard broad host range plasmid capable of replication in K. rhaeticus and E. coli (a shuttle vector) and was selected because the registry's standard plasmid backbone pSB1C3 can not be used for K. rhaeticus engineering.

NOTE: Because the registry's standard plasmid backbone pSB1C3 is not capable of replication in Komagataeibacter or Gluconacetobacter species, the Komagataeibacter 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 Komagataeibacter toolkit available for the synthetic biology community, Imperial iGEM 2014 team has made it freely available in AddGene or upon request.

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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 __NOTOC__
 <partinfo>BBa_K1321325 short</partinfo>
-x
+This plasmid encodes for LuxR generator and mRFP1 behind pLux promoter, making mRFP1 inducible via AHL, in pSEVA331Bb backbone. See attached file for annotated sequence. This construct is a member of the ''Komagataeibacter'' genetic engineering toolkit (parts BBa_K1321295 - BBa_K1321332). [[File:IC14_pLux02.gb]]
+''Komagataeibacter'' toolkit was designed to ease genetic engineering of cellulose-based biomaterials using the cellulose synthesizing bacterium ''Komagataeibacter rhaeticus iGEM'' (parts Bba_K1321305 and BBa_K1321306). As no registry parts had been tested in ''K. rhaeticus'', the aim of this toolkit was to determine the parts usable in ''K. rhaeticus'' and to characterize them in this host. pSEVA331-Bb is a non-standard broad host range plasmid capable of replication in ''K. rhaeticus'' and ''E. coli'' (a shuttle vector) and was selected because the registry's standard plasmid backbone pSB1C3 can not be used for ''K. rhaeticus'' engineering.
+NOTE: Because the registry's standard plasmid backbone pSB1C3 is not capable of replication in ''Komagataeibacter or Gluconacetobacter'' species, the ''Komagataeibacter'' 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 ''Komagataeibacter'' toolkit available for the synthetic biology community, Imperial iGEM 2014 team has made it freely available in AddGene or upon request.
 <!-- Add more about the biology of this part here