A new pathway for vacuolar cadmium sequestration in Saccharomyces cerevisiae: YCF1-catalyzed transport of bis(glutathionato)cadmium

被引:489
作者
Li, ZS [1 ]
Lu, YP [1 ]
Zhen, RG [1 ]
Szczypka, M [1 ]
Thiele, DJ [1 ]
Rea, PA [1 ]
机构
[1] UNIV MICHIGAN,SCH MED,DEPT BIOL CHEM,ANN ARBOR,MI 48109
关键词
ATP binding cassette transport protein; glutathione S-conjugate transporter; yeast cadmium factor protein; vacuolar membrane;
D O I
10.1073/pnas.94.1.42
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The yeast cadmium factor (YCF1) gene encodes an MgATP-energized glutathione S-conjugate transporter responsible for the vacuolar sequestration of organic compounds after their S-conjugation with glutathione. However, while YCF1 was originally isolated according to its ability to confer resistance to cadmium salts, neither its mode of interaction with Cd2+ nor the relationship between this process and organic glutathione-conjugate transport are known. Here we show through direct comparisons between vacuolar membrane vesicles purified from Saccharomyces cerevisiae strain DTY167, harboring a deletion of the YCF1 gene, and the isogenic wild-type strain DTY165 that YCF1 mediates the MgATP-energized vacuolar accumulation of Cd . glutathione complexes, The substrate requirements, kinetics and Cd2+/ glutathione stoichiometry of cadmium uptake and the molecular weight of the transport-active complex demonstrate that YCF1 selectively catalyzes the transport of bis(glutathionato)cadmium (Cd . GS(2)). On the basis of these results-the Cd2+ hypersensitivity of DTY167, versus DTY165, cells, the inducibility of YCF1-mediated transport, and the rapidity and spontaneity of Cd . GS(2) formation-this new pathway is concluded to contribute substantially to Cd2+ detoxification.
引用
收藏
页码:42 / 47
页数:6
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