Difference between revisions of "Part:BBa K743006"
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The use of [https://parts.igem.org/Part:BBa_K743000 BBa_K743000] and [https://parts.igem.org/Part:BBa_K743001 BBa_K743001] as recombination sites has no deleterious phenotypic effects on the cells. | The use of [https://parts.igem.org/Part:BBa_K743000 BBa_K743000] and [https://parts.igem.org/Part:BBa_K743001 BBa_K743001] as recombination sites has no deleterious phenotypic effects on the cells. | ||
| − | + | This part was used by [http://2012.igem.org/Team:UC_Chile UC_Chile 2012 team] to succesfully transform <i>Synechocystis PCC6803</i>. | |
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Latest revision as of 19:32, 24 September 2012
psb1C3_IntK recombination plasmid for Synechocystis PCC6803
This plasmid is intended to be used as a starting backbone for further addition of DNA parts by Gibson assembly between RS1 and KanR. As Synechocystis PCC6803 undergoes double homologous recombination naturally , any sequence between RS1 and RS2 will be introduced into its chromosome along with a KanR gene for selection in cyanobacteria or in E. coli.
The plasmid backbone also has a Chloramphenicol resistance casette for selection in E.coli only. The use of BBa_K743000 and BBa_K743001 as recombination sites has no deleterious phenotypic effects on the cells.
This part was used by [http://2012.igem.org/Team:UC_Chile UC_Chile 2012 team] to succesfully transform Synechocystis PCC6803.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1774
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1774
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1774
Illegal XhoI site found at 2271 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1774
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1774
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 511