Sucrose fermentation by Saccharomyces cerevisiae lacking hexose transport

被引:39
作者
Batista, AS [1 ]
Miletti, LC [1 ]
Stambuk, BU [1 ]
机构
[1] Univ Fed Santa Catarina, Dept Bioquim, Ctr Ciencias Biol, BR-88040900 Florianopolis, SC, Brazil
关键词
Sucrose-H+ symport; AGT1; hxt-null; Saccharomyces cerevisiae;
D O I
10.1159/000082078
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
Sucrose is the major carbon source used by Saccharomyces cerevisiae during production of baker's yeast, fuel ethanol and several distilled beverages. It is generally accepted that sucrose fermentation proceeds through extracellular hydrolysis of the sugar, mediated by the periplasmic invertase, producing glucose and fructose that are transported into the cells and metabolized. In the present work we analyzed the contribution to sucrose fermentation of a poorly characterized pathway of sucrose utilization by S. cerevisiae cells, the active transport of the sugar through the plasma membrane and its intracellular hydrolysis. A yeast strain that lacks the major hexose transporters (hxt1-hxt7 and gal2) is incapable of growing on or fermenting glucose or fructose. Our results show that this hxt-null strain is still able to ferment sucrose due to direct uptake of the sugar into the cells. Deletion of the AGT1 gene, which encodes a high-affi nity sucrose-H+ symporter, rendered cells incapable of sucrose fermentation. Since sucrose is not an inducer of the permease, expression of the AGT1 must be constitutive in order to allow growth of the hxt-null strain on sucrose. The molecular characterization of active sucrose transport and fermentation by S. cerevisiae cells opens new opportunities to optimize yeasts for sugar-cane-based industrial processes. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:26 / 33
页数:8
相关论文
共 53 条
[1]   Regulation of the Hansenula polymorpha maltase gene promoter in H-polymorpha and Saccharomyces cerevisiae [J].
Alamäe, T ;
Pärn, P ;
Viigand, K ;
Karp, H .
FEMS YEAST RESEARCH, 2003, 4 (02) :165-173
[2]  
Ausubel FM, 1995, SHORT PROTOCOLS MOL
[3]  
Bajaj BK, 2003, J SCI IND RES INDIA, V62, P1079
[4]  
BARFORD JP, 1992, BIOPROCESS ENG, V7, P303, DOI 10.1007/BF00705159
[5]  
Burrows S., 1959, J I BREWING, V65, P39
[6]   2 DIFFERENTIALLY REGULATED MESSENGER-RNAS WITH DIFFERENT 5' ENDS ENCODE SECRETED AND INTRACELLULAR FORMS OF YEAST INVERTASE [J].
CARLSON, M ;
BOTSTEIN, D .
CELL, 1982, 28 (01) :145-154
[7]   Carbon catabolite repression of invertase during batch cultivations of Saccharomyces cerevisiae:: the role of glucose, fructose, and mannose [J].
Dynesen, J ;
Smits, HP ;
Olsson, L ;
Nielsen, J .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1998, 50 (05) :579-582
[8]   Fed-batch culture of Sacchoromyces cerevisiae in sugar-cane blackstrap molasses:: invertase activity of intact cells in ethanol fermentation [J].
Echegaray, OF ;
Carvalho, JCM ;
Fernandes, ANR ;
Sato, S ;
Aquarone, E ;
Vitolo, M .
BIOMASS & BIOENERGY, 2000, 19 (01) :39-50
[9]   Genome-wide expression analyses:: Metabolic adaptation of Saccharomyces cerevisiae to high sugar stress [J].
Erasmus, DJ ;
van der Merwe, GK ;
van Vuuren, HJJ .
FEMS YEAST RESEARCH, 2003, 3 (04) :375-399
[10]  
Evans IH., 1990, YEAST TECHNOLOGY, P13