The salt tolerant yeast Zygosaccharomyces rouxii possesses two plasma-membrane Na+/H+-antiporters (ZrNha1p and ZrSod2-22p) playing different roles in cation homeostasis and cell physiology
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
18761413
DOI
10.1016/j.fgb.2008.08.001
PII: S1087-1845(08)00158-8
Knihovny.cz E-resources
- MeSH
- Sodium Chloride metabolism MeSH
- Gene Expression MeSH
- Fungal Proteins genetics metabolism MeSH
- Homeostasis * MeSH
- Cations metabolism MeSH
- Molecular Sequence Data MeSH
- Sodium-Hydrogen Exchangers genetics metabolism MeSH
- Amino Acid Sequence MeSH
- Sequence Deletion MeSH
- Sequence Alignment MeSH
- Zygosaccharomyces genetics physiology MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Sodium Chloride MeSH
- Fungal Proteins MeSH
- Cations MeSH
- Sodium-Hydrogen Exchangers MeSH
Antiporters exporting Na(+) and K(+) in exchange for protons are conserved among yeast species. The only exception so far has been Zygosaccharomyces rouxii, an osmotolerant species closely related to Saccharomyces cerevisiae. Z. rouxii was described as possessing one plasma-membrane antiporter transporting only Na(+) (ZrSod2-22p in the CBS 732(T) type strain). We report the characterization of a second gene, ZrNHA1, encoding a new K(+)(Na(+))/H(+)-antiporter capable of both K(+) and Na(+) export. Synteny analyses suggested that ZrSOD2-22 originated by single duplication of the ZrNHA1 gene. Substrate specificities and transport properties of ZrNha1p and ZrSod2-22p were compared upon heterologous expression in S. cerevisiae, and then directly in Z. rouxii. Deletion mutants and phenotype analyses revealed that ZrSod2-22 antiporter is important for Na(+) detoxification, probably together with ZrEna1 ATPase; ZrNha1p is indispensable to maintain potassium homeostasis and ZrEna1p is not, in contrast to the situation in S. cerevisiae, involved in this function.
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