Pribylova Lenka, Papouskova Klara, Sychrova Hana
Department of Membrane Transport, Institute of Physiology AS CR, v.v.i., Videnska 1083, 14220 Prague 4, Czech Republic.
Fungal Genet Biol. 2008 Oct;45(10):1439-47. doi: 10.1016/j.fgb.2008.08.001. Epub 2008 Aug 14.
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.
以质子交换方式输出Na⁺和K⁺的反向转运蛋白在酵母物种中是保守的。到目前为止,唯一的例外是鲁氏接合酵母,它是一种与酿酒酵母密切相关的耐渗透压物种。鲁氏接合酵母被描述为拥有一种仅转运Na⁺的质膜反向转运蛋白(CBS 732(T)型菌株中的ZrSod2 - 22p)。我们报道了第二个基因ZrNHA1的特征,它编码一种新的能够输出K⁺和Na⁺的K⁺(Na⁺)/H⁺反向转运蛋白。共线性分析表明ZrSOD2 - 22是由ZrNHA1基因的单次复制产生的。在酿酒酵母中进行异源表达后,然后直接在鲁氏接合酵母中,比较了ZrNha1p和ZrSod2 - 22p的底物特异性和转运特性。缺失突变体和表型分析表明,ZrSod2 - 22反向转运蛋白可能与ZrEna1 ATP酶一起对Na⁺解毒很重要;与酿酒酵母的情况相反,ZrNha1p对于维持钾离子稳态是不可或缺的,而ZrEna1p不参与此功能。