Chang Y S, Dubin R A, Perkins E, Michels C A, Needleman R B
Department of Biochemistry, Wayne State University School of Medicine, Detroit, Michigan 48201.
J Bacteriol. 1989 Nov;171(11):6148-54. doi: 10.1128/jb.171.11.6148-6154.1989.
Saccharomyces yeasts ferment several alpha-glucosides including maltose, maltotriose, turanose, alpha-methylglucoside, and melezitose. In the utilization of these sugars transport is the rate-limiting step. Several groups of investigators have described the characteristics of the maltose permease (D. E. Kroon and V. V. Koningsberger, Biochim. Biophys. Acta 204:590-609, 1970; R. Serrano, Eur. J. Biochem. 80:97-102, 1977). However, Saccharomyces contains multiple alpha-glucoside transport systems, and these studies have never been performed on a genetically defined strain shown to have only a single permease gene. In this study we isolated maltose-negative mutants in a MAL6 strain and, using a high-resolution mapping technique, we showed that one class of these mutants, the group A mutants, mapped to the MAL61 gene (a member of the MAL6 gene complex). An insertion into the N-terminal-coding region of MAL61 resulted in the constitutive production of MAL61 mRNA and rendered the maltose permease similarly constitutive. Transformation by high-copy-number plasmids containing the MAL61 gene also led to an increase in the maltose permease. A deletion-disruption of MAL61 completely abolished maltose transport activity. Taken together, these results prove that this strain has only a single maltose permease and that this permease is the product of the MAL61 gene. This permease is able to transport maltose and turanose but cannot transport maltotriose, alpha-methylglucoside, or melezitose. The construction of strains with only a single permease will allow us to identify other maltose-inducible transport systems by simple genetic tests and should lead to the identification and characterization of the multiple genes and gene products involved in alpha-glucoside transport in Saccharomyces yeasts.
酿酒酵母能发酵多种α-葡萄糖苷,包括麦芽糖、麦芽三糖、松二糖、α-甲基葡萄糖苷和蜜三糖。在利用这些糖类时,转运是限速步骤。几组研究人员描述了麦芽糖通透酶的特性(D.E. Kroon和V.V. Koningsberger,《生物化学与生物物理学报》204:590 - 609,1970;R. Serrano,《欧洲生物化学杂志》80:97 - 102,1977)。然而,酿酒酵母含有多种α-葡萄糖苷转运系统,且这些研究从未在经基因鉴定仅具有单个通透酶基因的菌株上进行过。在本研究中,我们在MAL6菌株中分离出麦芽糖阴性突变体,并使用高分辨率定位技术表明,这些突变体中的一类,即A组突变体,定位于MAL61基因(MAL6基因复合体的一个成员)。插入到MAL61的N端编码区导致MAL61 mRNA的组成型产生,并使麦芽糖通透酶同样组成型表达。用含有MAL61基因的高拷贝数质粒转化也导致麦芽糖通透酶增加。MAL61的缺失破坏完全消除了麦芽糖转运活性。综上所述,这些结果证明该菌株仅具有单个麦芽糖通透酶,且该通透酶是MAL61基因的产物。这种通透酶能够转运麦芽糖和松二糖,但不能转运麦芽三糖、α-甲基葡萄糖苷或蜜三糖。构建仅具有单个通透酶的菌株将使我们能够通过简单的遗传测试鉴定其他麦芽糖诱导的转运系统,并应导致对酿酒酵母中参与α-葡萄糖苷转运的多个基因和基因产物的鉴定和表征。