Composite

Part:BBa_K191003:Design

Designed by: Le Thanh Tu NGUYEN   Group: iGEM09_EPF-Lausanne   (2009-10-11)
Revision as of 13:25, 21 October 2009 by Nltt1987 (Talk | contribs) (→‎Source)

Promoter Lac I - RBS - LovTAP - Term


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 370
    Illegal PstI site found at 627
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal PstI site found at 370
    Illegal PstI site found at 627
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 370
    Illegal PstI site found at 627
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 370
    Illegal PstI site found at 627
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 764


Design Notes

  • Notice : 2 restriction sites of PstI in LovTAP sequence so LovTAP can't be cut with PstI.


  • LovTAP was obtained by PCR and ligated into double-term plasmid ( LovTAP was cut with E and S, plasmid E and X)
  • LOVTAP-Term is then amplified by PCR and cut with E and X to be put into another plasmid of high-copy and only Kanamycine resistance.
  • LacI was ligated into RBS
  • PCR on LacI-RBS, digestion with E and S then ligated into LovTAP-Term plasmid which was cut by E and X.

Source

BBa_R0010, BBa_B0030, BBa_B0015.

Plasmid containing LovTAP gene was kindly provided by the authors of : Light-activated DNA binding in a designed allosteric protein; Strickland et al., Proceedings of the National Academy of Sciences (2008) vol. 105 (31) pp. 10709

References

Light-activated DNA binding in a designed allosteric protein; Strickland et al., Proceedings of the National Academy of Sciences (2008) vol. 105 (31) pp. 10709