Difference between revisions of "Part:BBa K3279006:Design"

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===Source===
 
===Source===
  
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The sequence is original from Pseudomonas syringae's genomic sequence, and we did a codon optimization.
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The sequence is originally from Pseudomonas syringae's genomic DNA and we made the codon optimization.
  
 
===References===
 
===References===

Latest revision as of 14:22, 18 October 2019


INP-N ( N-terminus of Ice-nucleation protein ) from Pseudomonas syringae


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 333
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 75
    Illegal NgoMIV site found at 408
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

The primary concern was BioBrick compatibility so that illegal sites in RFC[10] did not appear in the sequence. And the sequeces was finally designed to link with pET30a(+) and cenA gene/cex gene, so we added restriction enzyme cutting site NdeI at the 5' and EcoRV at the 3'.


Source

The sequence is originally from Pseudomonas syringae's genomic DNA and we made the codon optimization.

References