Role of hexose transport in control of glycolytic flux in Saccharomyces cerevisiae

被引:87
作者
Elbing, K
Larsson, C
Bill, RM
Albers, E
Snoep, JL
Boles, E
Hohmann, S
Gustafsson, L
机构
[1] Chalmers Univ Technol, Dept Chem & Biosci Mol Biotechnol, SE-40530 Gothenburg, Sweden
[2] Univ Gothenburg, Dept Cell & Mol Biol Microbiol, Gothenburg, Sweden
[3] Aston Univ, Sch Life & Hlth Sci, Birmingham, W Midlands, England
[4] Univ Stellenbosch, Dept Biochem, Matieland, South Africa
[5] Univ Frankfurt, Inst Mikrobiol, Frankfurt, Germany
关键词
D O I
10.1128/AEM.70.9.5323-5330.2004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The yeast Saccharomyces cerevisiae predominantly ferments glucose to ethanol at high external glucose concentrations, irrespective of the presence of oxygen. In contrast, at low external glucose concentrations and in the presence of oxygen, as in a glucose-limited chemostat, no ethanol is produced. The importance of the external glucose concentration suggests a central role for the affinity and maximal transport rates of yeast's glucose transporters in the control of ethanol production. Here we present a series of strains producing functional chimeras between the hexose transporters Hxt1 and Hxt7, each of which has distinct glucose transport characteristics. The strains display a range of decreasing glycollytic rates resulting in a proportional decrease in ethanol production. Using these strains, we show for the first time that at high glucose levels, the glucose uptake capacity of wild-type S. cerevisiae does not control glycolytic flux during exponential batch growth. In contrast, our chimeric Hxt transporters control the rate of glycollysis to a high degree. Strains whose glucose uptake is mediated by these chimeric transporters will undoubtedly provide a powerful tool with which to examine in detail the mechanism underlying the switch between fermentation and respiration in S. cerevisiae and will provide new tools for the control of industrial fermentations.
引用
收藏
页码:5323 / 5330
页数:8
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