Difference between revisions of "Part:BBa K615003"
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This one-hybrid strain uses TolC as both a negative and positive selector. As a membrane pump that removes toxins from the cell, TolC is needed for the cell to survive in media containing SDS. If the zinc finger expressed in the cell successfully binds to the binding site upstream of the TolC gene, TolC will be expressed and the cell will live. If the zinc finger does not bind, TolC will not be expressed and the cell will not be able to pump out the SDS. Additionally, the strain can be grown in media with colicin before zinc fingers are added to the cells. Colicin is a toxin that needs TolC to enter the cell, and so any cells containing constitutively active promoters would die while those without leaky promoters would live. | This one-hybrid strain uses TolC as both a negative and positive selector. As a membrane pump that removes toxins from the cell, TolC is needed for the cell to survive in media containing SDS. If the zinc finger expressed in the cell successfully binds to the binding site upstream of the TolC gene, TolC will be expressed and the cell will live. If the zinc finger does not bind, TolC will not be expressed and the cell will not be able to pump out the SDS. Additionally, the strain can be grown in media with colicin before zinc fingers are added to the cells. Colicin is a toxin that needs TolC to enter the cell, and so any cells containing constitutively active promoters would die while those without leaky promoters would live. | ||
− | The strain has been shown to have the proper growth phenotype in SDS. Currently the binding site is for Zif268, but this can be easily changed using lambda red. When Zif268 is diluted into different amounts of negative control zinc fingers, the strain is able to recognize a valid hit in a dilution of one to one hundred. | + | The strain has been shown to have the proper growth phenotype in SDS. Currently the binding site is for Zif268, but this can be easily changed using lambda red. When Zif268 is diluted into different amounts of negative control zinc fingers, the strain is able to recognize a valid hit in a dilution of no greater than one to one hundred. |
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+ | [[Image: HARVtolc.png]] | ||
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Revision as of 03:41, 27 September 2011
E. coli strain for TolC one-hybrid selection system
This strain is designed to test zinc finger binding by tying the binding event to cell survival, specifically the expression of TolC, a membrane pump that removes toxins from the cell. The omega subunit of RNA polymerase has been knocked out using lambda red to replace the gene with a zeocin cassette, and the strain is designed to be used in conjunction with a zinc finger-omega subunit fusion protein. See below for a summary of features and techniques.
Usage and Biology
This one-hybrid strain uses TolC as both a negative and positive selector. As a membrane pump that removes toxins from the cell, TolC is needed for the cell to survive in media containing SDS. If the zinc finger expressed in the cell successfully binds to the binding site upstream of the TolC gene, TolC will be expressed and the cell will live. If the zinc finger does not bind, TolC will not be expressed and the cell will not be able to pump out the SDS. Additionally, the strain can be grown in media with colicin before zinc fingers are added to the cells. Colicin is a toxin that needs TolC to enter the cell, and so any cells containing constitutively active promoters would die while those without leaky promoters would live.
The strain has been shown to have the proper growth phenotype in SDS. Currently the binding site is for Zif268, but this can be easily changed using lambda red. When Zif268 is diluted into different amounts of negative control zinc fingers, the strain is able to recognize a valid hit in a dilution of no greater than one to one hundred.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 632
Illegal PstI site found at 952 - 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 632
Illegal PstI site found at 952 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 845
Illegal BglII site found at 965 - 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 632
Illegal PstI site found at 952 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 632
Illegal PstI site found at 952
Illegal NgoMIV site found at 181 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 121
Illegal SapI site found at 331