A CDC25 homologue from rice functions as an arsenate reductase

被引:126
作者
Duan, Gui-Lan
Zhou, Yao
Tong, Yi-Ping
Mukhopadhyay, Rita
Rosen, Barry P.
Zhu, Yong-Guan
机构
[1] Chinese Acad Sci, Ecoenvironm Sci Res Ctr, Dept Soil Environm Sci, Beijing 100085, Peoples R China
[2] Wayne State Univ, Sch Med, Dept Biochem & Mol Biol, Detroit, MI 48201 USA
[3] Chinese Acad Sci, Inst Genet & Dev Biol, Beijing 100083, Peoples R China
关键词
arsenate reductase; arsenic speciation; CDC25 (cell division cycle); metabolism; rice (Oryza sativa); transcriptional patterns;
D O I
10.1111/j.1469-8137.2007.02009.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Enzymatic reduction of arsenate to arsenite is the first step in arsenate metabolism in all organisms studied. The rice genome contains two ACR2-like genes, OsACR2.1 and OsACR2.2, which may be involved in regulating arsenic metabolism in rice. Here, we cloned both OsACR2 genes and expressed them in an Escherichia coli strain in which the arsC gene was deleted and in a yeast (Saccharomyces cerevisiae) strain with a disrupted ACR2 gene. OsACR2.1 complemented the arsenate hypersensitive phenotype of E. coli and yeast. OsACR2.2 showed much less ability to complement. The gene products were purified and demonstrated to reduce arsenate to arsenite in vitro, and both exhibited phosphatase activity. In agreement with the complementation results, OsACR2.1 exhibited higher reductase activity than OsACR2.2. Mutagenesis of cysteine residues in the putative active site HC(X)(5)R motif led to nearly complete loss of both phosphatase and arsenate reductase activities. In planta expression of OsACR2.1 increased dramatically after exposure to arsenate. OsACR2.2 was observed only in roots following arsenate exposure, and its expression was less than OsACR2.1.
引用
收藏
页码:311 / 321
页数:11
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