Literature DB >> 19916929

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

V V Petrov1.   

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.

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Year:  2009        PMID: 19916929     DOI: 10.1134/s0006297909100125

Source DB:  PubMed          Journal:  Biochemistry (Mosc)        ISSN: 0006-2979            Impact factor:   2.487


  1 in total

1.  Mechanism of proanthocyanidins-induced alcoholic fermentation enhancement in Saccharomyces cerevisiae.

Authors:  Jingyuan Li; Hongwei Zhao; Weidong Huang
Journal:  J Ind Microbiol Biotechnol       Date:  2014-10-02       Impact factor: 3.346

  1 in total

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