Reporter

Part:BBa_K861175

Designed by: Kuanwei Shneg, Xian Xia   Group: iGEM12_WHU-China   (2012-09-08)
Revision as of 17:31, 21 September 2012 by Shinkwee (Talk | contribs)

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Efficacy testing RFP generator of BBa_K861170 (PI)

PI promoter contains the altered consensus CRP-binding site and the consensus RNA polymerase-binding site which have a overlap of several base pairs. Therefore, due to the steric hindrance between CRP and RNA polymerase, gene downstream of the promoter will be repressed at high concentration of CRP.In the cells ,low glucose concentration results in increased activity by adenylate cyclase. cAMP binds to the cAMP receptor protein, which, in its bound form, is able to bind tightly to the specific DNA site in the promoter and repress the gene downstream. On the contrary, high glucose concentration will result in the expression of the promoter. RFP was used to test the function of PI.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 617
    Illegal AgeI site found at 729
  • 1000
    COMPATIBLE WITH RFC[1000]


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Parameters
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