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AUTHORS |
J. L. Hobman & N. L. Brown
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INSTITUTION |
School of Biological Sciences, University of Birmingham, Edgbaston, UK.
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TITLE |
Overexpression of MerT, the mercuric ion transport protein of transposon Tn501, and genetic selection of mercury hypersensitivity mutations.
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SOURCE |
Mol. Gen. Genet. 250: 129-134 (1996)[96158853]
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COUNTRY OF PUBLICATION |
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ABSTRACT |
The small (116 amino acids) inner membrane protein MerT encoded by the
transposon Tn501 has been overexpressed under the control of the bacteriophage
T7 expression system. Random mutants of MerT were made and screened for loss of
mercuric ion hypersensitivity. Several mutant merT genes were selected and
sequenced: Cys24Arg and Cys25Tyr mutations abolish mercury resistance, as do
charge-substitution mutations in the first predicted transmembrane helix (Gly14Arg,
Gly15Arg, Gly27Arg, Ala18Asp), and the termination mutations Trp66Ter and
Cys82Ter.
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PUBLICATION TYPE |
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LANGUAGE |
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