Device
iccdB0.07

Part:BBa_K658005:Design

Designed by: Yidan Hu   Group: iGEM11_XMU-China   (2011-09-29)
Revision as of 03:29, 6 October 2011 by Xmuwendy (Talk | contribs) (→‎References)

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a bacteria population-control device with RBS0.07 driven by lacl+pL


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 718
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 2346
    Illegal BsaI.rc site found at 1874


Design Notes

Design considerations are the same as BBa_K658003

Source

BBa_K658003

References

[1]Miki T,Yoshioka K,Horiuchi T. Control of cell division by sex factor F in Escherichia coli. I. The 42.84-43.6 F segment couples cell division of the host bacteria with replication of plasmid DNA. Molecular Biology,1984,177(4):605-625.

[2] http://en.wikipedia.org/wiki/N-Acyl_homoserine_lactone

[3] Hanzelka BL, Greenberg E. Quorum sensing in Vibrio fischeri: evidence that S-adenosyl methionine is the amino acid substrate for autoinducer synthesis[J]. Journal of Bacteriology, 1996, 178(17): 5291-5294.

[4] Urbanowski M, Lostroh C, Greenberg E. Reversible acyl-homoserine lactone binding to purified Vibrio fischeri LuxR protein[J]. Journal of Bacteriology, 2004, 186(3): 631-637.

[5] Hansen LH, Knudsen S, Sorensen SJ . The effect of the lacY gene on the induction of IPTG inducible promoters, studied in Escherichia coli and Pseudomonas fluorescens. Curr microbiol，1998， 36 (6): 341–345.

[6]Bernard P，Couturier M. Cell killing by the F plasmid CcdB protein involves poisoning of DNA-topoisomerase II complexes. Molecular Biology,1992,226:735-745.

[7]Semit M.H,Duin J. Secondary structure of the ribosome binding site determines translational efficiency: a quantitative analysis. Molecular Biology,1990,87(19):7668-7672.