Isolation of two cell populations from yeast during high-level alcoholic fermentation that resemble quiescent and nonquiescent cells from the stationary phase on glucose

被引:21
作者
Benbadis, Laurent [1 ,2 ,3 ]
Cot, Marlene [1 ,2 ,3 ]
Rigoulet, Michel [4 ]
Francois, Jean [1 ,2 ,3 ]
机构
[1] Univ Toulouse, INSA, UPS, INP,LISBP, F-31077 Toulouse, France
[2] INRA, UMR792, Toulouse, France
[3] CNRS, UMR5504, Toulouse, France
[4] Inst Biochim & Genet Cellulaires, CNRS, UMR5095, Bordeaux, France
关键词
fermentation; ethanol tolerance; quiescence; energetic; yeast; SACCHAROMYCES-CEREVISIAE; ETHANOL TOLERANCE; GENE-EXPRESSION; HYDROGEN-PEROXIDE; N-ACETYLCYSTEINE; VIABILITY; STRESS; IDENTIFICATION; GLUTATHIONE; METABOLISM;
D O I
10.1111/j.1567-1364.2009.00553.x
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
High-level production of bioethanol (140 g L-1 in 45 h) in aerated fed-batch cultures of Saccharomyces cerevisiae was shown to be linked to the length of a production phase uncoupled to the growth. The induction of this phase was characterized by metabolic and morphologic changes reminiscent of those occurring in the stationary phase of growth on glucose. Global transcriptomic analysis of ethanol-stressed yeast cells in the uncoupling phase harboured features similar to those from stationary-phase cells on glucose. Two distinct cellular populations were isolated by Percoll density-gradient centrifugation in this uncoupling phase. The lower fraction was enriched by yeast cells that were mostly uniform in size and opalescent, containing a large amount of glycogen and trehalose, and exhibiting high respiratory activity. In contrast, the upper fraction was characterized by cells heterogeneous in size, with one to several small buds, which did not contain storage carbohydrates and which exhibited a poor respiratory competence while retaining a high relative glycolytic activity. These results are discussed in terms of a possible induction of a state similar to the quiescence state previously observed from yeast stationary-phase cultures, in response to ethanol toxicity, whose acquisition may be critical for performing high-level alcoholic fermentation.
引用
收藏
页码:1172 / 1186
页数:15
相关论文
共 49 条
[1]   ROLE OF MITOCHONDRIA IN ETHANOL TOLERANCE OF SACCHAROMYCES-CEREVISIAE [J].
AGUILERA, A ;
BENITEZ, T .
ARCHIVES OF MICROBIOLOGY, 1985, 142 (04) :389-392
[2]   Alteration in membrane fluidity and lipid composition, and modulation of H+-ATPase activity in Saccharomyces cerevisiae caused by decanoic acid [J].
Alexandre, H ;
Mathieu, B ;
Charpentier, C .
MICROBIOLOGY-SGM, 1996, 142 :469-475
[3]   Global gene expression during short-term ethanol stress in Saccharomyces cerevisiae [J].
Alexandre, H ;
Ansanay-Galeote, V ;
Dequin, S ;
Blondin, B .
FEBS LETTERS, 2001, 498 (01) :98-103
[4]   Aeration strategy:: a need for very high ethanol performance in Saccharomyces cerevisiae fed-batch process [J].
Alfenore, S ;
Cameleyre, X ;
Benbadis, L ;
Bideaux, C ;
Uribelarrea, JL ;
Goma, G ;
Molina-Jouve, C ;
Guillouet, SE .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2004, 63 (05) :537-542
[5]   Improving ethanol production and viability of Saccharomyces cerevisiae by a vitamin feeding strategy during fed-batch process [J].
Alfenore, S ;
Molina-Jouve, C ;
Guillouet, SE ;
Uribelarrea, JL ;
Goma, G ;
Benbadis, L .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2002, 60 (1-2) :67-72
[6]   Isolation of quiescent and nonquiescent cells from yeast stationary-phase cultures [J].
Allen, Chris ;
Buettner, Sabrina ;
Aragon, Anthony D. ;
Thomas, Jason A. ;
Meirelles, Osorio ;
Jaetao, Jason E. ;
Benn, Don ;
Ruby, Stephanie W. ;
Veenhuis, Marten ;
Madeo, Frank ;
Werner-Washburne, Margaret .
JOURNAL OF CELL BIOLOGY, 2006, 174 (01) :89-100
[7]   Characterization of differentiated quiescent and nonquiescent cells in yeast stationary-phase cultures [J].
Aragon, Anthony D. ;
Rodriguez, Angelina L. ;
Meirelles, Osorio ;
Roy, Sushmita ;
Davidson, George S. ;
Tapia, Phillip H. ;
Allen, Chris ;
Joe, Ray ;
Benn, Don ;
Werner-Washburne, Margaret .
MOLECULAR BIOLOGY OF THE CELL, 2008, 19 (03) :1271-1280
[8]   THE ANTIOXIDANT ACTION OF N-ACETYLCYSTEINE - ITS REACTION WITH HYDROGEN-PEROXIDE, HYDROXYL RADICAL, SUPEROXIDE, AND HYPOCHLOROUS ACID [J].
ARUOMA, OI ;
HALLIWELL, B ;
HOEY, BM ;
BUTLER, J .
FREE RADICAL BIOLOGY AND MEDICINE, 1989, 6 (06) :593-597
[9]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[10]  
CARDOSO H, 1992, FEMS MICROBIOL LETT, V94, P155