Difference between revisions of "Part:BBa K559011:Design"

 
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===References===
 
===References===
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[1]J.W. Sanders, G. Venema, and J. Kok, “A chloride-inducible gene expression cassette and its use in induced lysis of Lactococcus lactis,” ''Applied and environmental microbiology'', vol. 63, Dec. 1997, p. 4877.
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[2]J.W. Sanders, G. Venema, and J. Kok, “Identifcation of a sodium chloride-regulated promoter in Lactococcus lactis by single-copy chromosomal fusion with a reporter gene” ''Mol Gen Genet'', vol. 257, Dec. 1988, p. 681-685.

Revision as of 08:51, 28 October 2011

Pgad - Intracellular Chloride-Sensing Cassette


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

Synthesized part by GenScript,all the illegal sites for RFC 10 (EcoRI, XbaI, SpeI, PstI) have been substituted by other codon producing the same amino acid in E. coli.


Source

The gene sequence was obtained from the cassette from bp 821 to 2071 of GenBank sequence AF005098, which includes PgadR, gadR, Pgad and the starting codon ATG.

References

[1]J.W. Sanders, G. Venema, and J. Kok, “A chloride-inducible gene expression cassette and its use in induced lysis of Lactococcus lactis,” Applied and environmental microbiology, vol. 63, Dec. 1997, p. 4877.

[2]J.W. Sanders, G. Venema, and J. Kok, “Identifcation of a sodium chloride-regulated promoter in Lactococcus lactis by single-copy chromosomal fusion with a reporter gene” Mol Gen Genet, vol. 257, Dec. 1988, p. 681-685.