Zinc dependence of zinT (yodA) mutants and binding of zinc, cadmium and mercury by ZinT

被引:31
作者
Kershaw, Christopher J. [1 ]
Brown, Nigel L. [1 ]
Hobman, Jon L. [1 ]
机构
[1] Univ Birmingham, Sch Business, Birmingham B15 2TT, W Midlands, England
基金
英国生物技术与生命科学研究理事会;
关键词
ZinT; YodA; zinc import; cadmium; mercury;
D O I
10.1016/j.bbrc.2007.09.094
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
ZinT (B1973), previously known as YodA, was originally characterised as a cadmium-induced periplasmic protein under the regulation of Fur and SoxS. Here we describe a decrease in zinT transcript in response to elevated copper concentrations and the zinc and copper dependent phenotype of a Delta zinT strain. Cadmium sensitivity of the Delta zinT strain was not observed. We demonstrate the binding of nickel, zinc, cadmium, and mercury, but not cobalt, copper, iron, and manganese, to purified ZinT using mass spectrometry. This and previous studies support the hypothesis that ZinT plays a role in zinc homeostasis and is required for growth under zinc limited conditions. suggesting that ZinT is either a periplasmic zinc chaperone or is involved in zinc import. Limited metal ion discrimination results in regulation of PzinT in a non-specific manner, which is mirrored in the binding of several different heavy metals by ZinT. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:66 / 71
页数:6
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