Difference between revisions of "Part:BBa K743006"

 
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<partinfo>BBa_K743006 short</partinfo>
 
<partinfo>BBa_K743006 short</partinfo>
  
This plasmid is intended to be used as a starting backbone for further adition of dna parts by Gibson assembly between RS1 and KanR. As synechocystis naturally undergoes double homologous recombination, any sequence between RS1 and RS2 will be introduced in to it´s chromosome along with a KanR gene for selection in cyanobacteria or in E.coli
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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.
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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  
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This part 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
 
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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


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 1774
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 1774
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 1774
    Illegal XhoI site found at 2271
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 1774
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 1774
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 511