Difference between revisions of "Part:BBa K3128011:Design"

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pUT18 plasmid from Euromedex BACTH kit was used.  
 
pUT18 plasmid from Euromedex BACTH kit was used.  
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OmpX gene was synthesized by IDT because it was unavailable on iGEM plates.
+
OmpX gene and GGS linker were synthesized by IDT because they were unavailable on iGEM plates.
  
 
===References===
 
===References===

Revision as of 17:03, 18 September 2019


OmpX-WT fused with T18 subpart of Bordetella Pertussis adenylate cyclase under lactose promoter


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 1504
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 1045
    Illegal NgoMIV site found at 1455
    Illegal AgeI site found at 1261
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

Euromedex BACTH kit contains the pUT18 plasmid with a MCS cassette followed by the T18 subpart of the Bordetella pertussis adenylate cyclase. It allows the cloning of the protein of interest in fusion with the T18 subpart. To respect RFC rules, the plasmid has been amplificated by PCR using primers that bind from either site of the MCS cassette to eliminate it. Those primers contain also restriction sites enabling the cloning of the protein in the system. The plasmid was digested by the corresponding enzymes and the protein gene was inserted.

Source

pUT18 plasmid from Euromedex BACTH kit was used. OmpX gene and GGS linker were synthesized by IDT because they were unavailable on iGEM plates.

References