Difference between revisions of "Part:BBa K624027"
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Shuttle vector between E. coli and Magnetospirillum magneticum AMB-1, containing [ori+Pmsp1+rep] (essentials of pYMB) on pUC19 | Shuttle vector between E. coli and Magnetospirillum magneticum AMB-1, containing [ori+Pmsp1+rep] (essentials of pYMB) on pUC19 | ||
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| + | *pYMB(Fig. 1) is described to contain the ori (origin of replication), rep gene (required for replication) of pMGT. Once the synthetic work had been done, pYMB is constructed by equipping the ori, the appropriate promoter for AMB-1 (Pmsp1 as our choice) and rep gene on the commercial plasmid pUC19 which was revised as the expression of Biobrick backbone psB1A1with promotor Pmsp1. The constructed vector is capable of replicating within both E. coli and AMB-1, fully sufficing a competent shuttle vector for genetic engineering the magnetotactic bateria.</font> | ||
| + | [[Image: PYMBWorkflow.jpg|center|frame|<center>Fig.1 pYMB Work Flow <br>The way we design the shuttle vector for magnetic bacteria</center>]] | ||
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Latest revision as of 07:53, 30 October 2011
pYMB (shuttle vector between Escherichia coli and Magnetospirillum magneticum AMB-1)
Shuttle vector between E. coli and Magnetospirillum magneticum AMB-1, containing [ori+Pmsp1+rep] (essentials of pYMB) on pUC19
- pYMB(Fig. 1) is described to contain the ori (origin of replication), rep gene (required for replication) of pMGT. Once the synthetic work had been done, pYMB is constructed by equipping the ori, the appropriate promoter for AMB-1 (Pmsp1 as our choice) and rep gene on the commercial plasmid pUC19 which was revised as the expression of Biobrick backbone psB1A1with promotor Pmsp1. The constructed vector is capable of replicating within both E. coli and AMB-1, fully sufficing a competent shuttle vector for genetic engineering the magnetotactic bateria.
The way we design the shuttle vector for magnetic bacteria
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal prefix found in sequence at 1
Illegal PstI site found at 1173 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1
Illegal PstI site found at 1173
Illegal NotI site found at 7
Illegal NotI site found at 1166 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1
- 23INCOMPATIBLE WITH RFC[23]Illegal prefix found in sequence at 1
Illegal PstI site found at 1173 - 25INCOMPATIBLE WITH RFC[25]Illegal prefix found in sequence at 1
Illegal XbaI site found at 16
Illegal PstI site found at 1173
Illegal NgoMIV site found at 920 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 2504
Illegal SapI site found at 1421
