Iwaki T, Higashida Y, Tsuji H, Tamai Y, Watanabe Y
Department of Biological Resources, Faculty of Agriculture, Ehime University, Japan.
Yeast. 1998 Sep 30;14(13):1167-74. doi: 10.1002/(SICI)1097-0061(19980930)14:13<1167::AID-YEA318>3.0.CO;2-5.
We reported in our previous paper on the characterization of the Na+/H(+)-antiporter gene (ZSOD2) closely related to the salt-tolerance of yeast Zygosaccharomyces rouxii. In the present paper, we have cloned a second gene (ZSOD22) of Na+/H+ antiporter from Z. rouxii. The deduced amino acid sequence of Zsod22p was highly homologous to that of Zsod2p, Sod2p from Schizosaccharomyces pombe, and Nhalp from Saccharomyces cerevisiae. The open reading frames (ORFs) from ZSOD2 or ZSOD22 were inserted into a yeast expression vector pYES2, and their constructs (pZSOD2 and pZSOD22) were used to transform the salt-sensitive S. cerevisiae. pZSOD2- or pZSOD22-harboring-recombinant S. cerevisiae cells showed increases in salt tolerance. However, the Z. rouxii disruptant of ZSOD22 did not show any phenotypes related to salt tolerance or osmotolerance, unlike that of ZSOD2. The transcriptional expression of ZSOD22 was not observed by Northern blot analysis even in Z. rouxii cells subjected to NaCl-shock. From these results we conclude that although Z. rouxii includes at least two copies of the Na+/H(+)-antiporter gene (ZSOD2 and ZSOD22), ZSOD2 encodes a functional product as an antiporter and ZSOD22 is poorly transcribed, if at all.
我们在之前的论文中报道了与鲁氏接合酵母耐盐性密切相关的Na⁺/H⁺逆向转运蛋白基因(ZSOD2)的特征。在本文中,我们从鲁氏接合酵母中克隆了第二个Na⁺/H⁺逆向转运蛋白基因(ZSOD22)。推导的Zsod22p氨基酸序列与Zsod2p、粟酒裂殖酵母的Sod2p以及酿酒酵母的Nhalp的氨基酸序列高度同源。将ZSOD2或ZSOD22的开放阅读框(ORF)插入酵母表达载体pYES2中,并用它们的构建体(pZSOD2和pZSOD22)转化盐敏感型酿酒酵母。携带pZSOD2或pZSOD22的重组酿酒酵母细胞的耐盐性增强。然而,与ZSOD2不同,ZSOD22的鲁氏接合酵母破坏株未表现出任何与耐盐性或耐渗透压性相关的表型。即使在经受NaCl冲击的鲁氏接合酵母细胞中,通过Northern印迹分析也未观察到ZSOD22的转录表达。从这些结果我们得出结论,尽管鲁氏接合酵母至少包含两个Na⁺/H⁺逆向转运蛋白基因拷贝(ZSOD2和ZSOD22),但ZSOD2编码一种作为逆向转运蛋白的功能产物,而ZSOD22即使转录也转录水平很低。