Difference between revisions of "Part:BBa K743006"
Juan Alamos (Talk | contribs) |
|||
Line 2: | Line 2: | ||
<partinfo>BBa_K743006 short</partinfo> | <partinfo>BBa_K743006 short</partinfo> | ||
− | This plasmid is intended to be used as a starting backbone for further | + | 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 <i>Synechocystis PCC6803</i> 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 <i>E. coli</i>. |
− | The plasmid backbone also has a Chloramphenicol resistance casette for selection in E.coli only. | + | |
+ | The plasmid backbone also has a Chloramphenicol resistance casette for selection in <i>E.coli</i> only. | ||
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. | ||
− | It was used by [http://2012.igem.org/Team:UC_Chile UC_Chile 2012 team] to succesfully transform Synechocystis | + | It was used by [http://2012.igem.org/Team:UC_Chile UC_Chile 2012 team] to succesfully transform <i>Synechocystis PCC6803</i>. |
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 19:31, 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.
It 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