Difference between revisions of "Part:BBa K3183005:Design"

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===References===
 
===References===
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Darkoh, Charles, et al. “Toxin Synthesis by Clostridium Difficile Is Regulated through Quorum Signaling.” MBio, vol. 6, no. 2, May 2015, pp. e02569-14. mbio.asm.org, doi:10.1128/mBio.02569-14.
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1. Essigmann, Heather T., et al. “The Clostridium Difficile Quorum-Sensing Molecule Alters the Staphylococcus Aureus Toxin Expression Profile.” International Journal of Antimicrobial Agents, vol. 49, no. 3, Mar. 2017, pp. 391–93. DOI.org (Crossref), doi:10.1016/j.ijantimicag.2017.01.001.
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Latest revision as of 22:24, 21 October 2019


AgrC2 Quorum Sensing Histidine Kinase; C. difficile


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

Codon optimized for L. reuteri using [http://www.kazusa.or.jp/codon/cgi-bin/showcodon.cgi?species=1598 kazusa codon-usage tables.]
RF10, 12, 21, 23, 25, and 1000 Compatible

Source

Derived from the C. difficile strain CD196 Genome; synthesized in IDT gBlocks.

References

Darkoh, Charles, et al. “Toxin Synthesis by Clostridium Difficile Is Regulated through Quorum Signaling.” MBio, vol. 6, no. 2, May 2015, pp. e02569-14. mbio.asm.org, doi:10.1128/mBio.02569-14.