Overexpression of MerT, the mercuric ion transport protein of transposon Tn501, and genetic selection of mercury hypersensitivity mutations |
| |
Authors: | Jonathan L. Hobman and Nigel L. Brown |
| |
Affiliation: | (1) Molecular Genetics and Cell Biology Research Group School of Biological Sciences, The University of Birmingham, B15 2TT Edgbaston, Birmingham, UK |
| |
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 mutantmerT genes were selected and sequenced: Cys24Arg and Cys25Tyr mutations abolish mercury resistance, as do charge-substitution mutations in the first predicted transmembrane helix (Glyl4Arg, Glyl5Arg, Gly27Arg, Ala18Asp), and the termination mutations Trp66Ter and Cys82Ter. |
| |
Keywords: | Mercury resistance Membrane protein function Mutagenesis Mercury hypersensitivity |
本文献已被 SpringerLink 等数据库收录! |
|