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携带最小数量半胱氨酸残基的酿酒酵母 Pma1 H+-ATPase 的功能。

Functioning of Saccharomyces cerevisiae Pma1 H+-ATPase carrying the minimal number of cysteine residues.

机构信息

Department of Genetics, Yale University School of Medicine, New Haven, CT 06510, USA.

出版信息

Biochemistry (Mosc). 2009 Oct;74(10):1155-63. doi: 10.1134/s0006297909100125.

Abstract

Pma1 H+-ATPase is the primary proton pump in the plasma membrane of the yeast Saccharomyces cerevisiae. It generates an electrochemical proton gradient, thus providing energy for secondary solute transport systems. The enzyme contains nine cysteines, three (Cys148, Cys312, and Cys867) in transmembrane segments and the rest (Cys221, Cys376, Cys409, Cys472, Cys532, and Cys569) in the cytosolic parts of the molecule. Although individually they are not essential for the functioning of the ATPase, substitution of all of them leads to the loss of enzyme activity and impairment of biogenesis. By means of site-directed mutagenesis combined with other molecular-biological and biochemical methods, this work defines different combinations of minimal cysteine content that are consistent with ATPase function.

摘要

Pma1 H+-ATPase 是酵母 Saccharomyces cerevisiae 质膜中的主要质子泵。它产生电化学质子梯度,从而为次级溶质转运系统提供能量。该酶含有 9 个半胱氨酸,其中 3 个(Cys148、Cys312 和 Cys867)位于跨膜片段中,其余(Cys221、Cys376、Cys409、Cys472、Cys532 和 Cys569)位于分子的胞质部分。尽管它们单独对于 ATPase 的功能不是必需的,但所有这些半胱氨酸的替换都会导致酶活性的丧失和生物发生的损害。通过结合其他分子生物学和生物化学方法的定点突变,这项工作定义了与 ATPase 功能一致的最小半胱氨酸含量的不同组合。

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