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酿酒酵母中Fps1依赖性和非依赖性甘油转运的特征

Characteristics of Fps1-dependent and -independent glycerol transport in Saccharomyces cerevisiae.

作者信息

Sutherland F C, Lages F, Lucas C, Luyten K, Albertyn J, Hohmann S, Prior B A, Kilian S G

机构信息

Department of Microbiology and Biochemistry, University of the Orange Free State, Bloemfontein, Republic of South Africa.

出版信息

J Bacteriol. 1997 Dec;179(24):7790-5. doi: 10.1128/jb.179.24.7790-7795.1997.

Abstract

Eadie-Hofstee plots of glycerol uptake in wild-type Saccharomyces cerevisiae W303-1A grown on glucose showed the presence of both saturable transport and simple diffusion, whereas an fps1delta mutant displayed only simple diffusion. Transformation of the fps1delta mutant with the glpF gene, which encodes glycerol transport in Escherichia coli, restored biphasic transport kinetics. Yeast extract-peptone-dextrose-grown wild-type cells had a higher passive diffusion constant than the fps1delta mutant, and ethanol enhanced the rate of proton diffusion to a greater extent in the wild type than in the fps1delta mutant. In addition, the lipid fraction of the fps1delta mutant contained a lower percentage of phospholipids and a higher percentage of glycolipids than that of the wild type. Fps1p, therefore, may be involved in the regulation of lipid metabolism in S. cerevisiae, affecting membrane permeability in addition to fulfilling its specific role in glycerol transport. Simultaneous uptake of glycerol and protons occurred in both glycerol- and ethanol-grown wild-type and fps1delta cells and resulted in the accumulation of glycerol at an inside-to-outside ratio of 12:1 to 15:1. Carbonyl cyanide m-chlorophenylhydrazone prevented glycerol accumulation in both strains and abolished transport in the fps1delta mutant grown on ethanol. Likewise, 2,4-dinitrophenol inhibited transport in glycerol-grown wild-type cells. These results indicate the presence of an Fps1p-dependent facilitated diffusion system in glucose-grown cells and an Fps1p-independent proton symport system in derepressed cells.

摘要

在以葡萄糖为生长底物的野生型酿酒酵母W303 - 1A中,甘油摄取的伊迪 - 霍夫斯蒂图显示存在可饱和转运和简单扩散,而fps1delta突变体仅表现出简单扩散。用编码大肠杆菌中甘油转运蛋白的glpF基因转化fps1delta突变体,恢复了双相转运动力学。酵母提取物 - 蛋白胨 - 葡萄糖培养基培养的野生型细胞比fps1delta突变体具有更高的被动扩散常数,并且乙醇在野生型中比在fps1delta突变体中更大程度地提高了质子扩散速率。此外,fps1delta突变体的脂质部分中磷脂的百分比低于野生型,糖脂的百分比高于野生型。因此,Fps1p可能参与酿酒酵母脂质代谢的调节,除了在甘油转运中发挥其特定作用外,还影响膜通透性。在甘油和乙醇培养的野生型和fps1delta细胞中均同时发生甘油和质子的摄取,导致甘油以12:1至15:1的内外比率积累。羰基氰化物间氯苯腙可阻止两种菌株中甘油的积累,并消除在乙醇上生长的fps1delta突变体中的转运。同样,2,4 - 二硝基苯酚抑制在甘油培养的野生型细胞中的转运。这些结果表明在葡萄糖培养的细胞中存在Fps1p依赖性促进扩散系统,在去阻遏细胞中存在Fps1p非依赖性质子同向转运系统。

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