The oxidative stress response of a lager brewing yeast strain during industrial propagation and fermentation

被引:56
作者
Gibson, Brian R. [1 ]
Lawrence, Stephen J. [1 ]
Boulton, Chris A. [1 ]
Box, Wendy G. [1 ]
Graham, Neil S. [1 ]
Linforth, Robert S. T. [1 ]
Smart, Katherine A. [1 ]
机构
[1] Univ Nottingham, Sch Biosci, Loughborough LE12 5RD, Leics, England
关键词
yeast; antioxidants; stress; brewing; propagation; fermentation;
D O I
10.1111/j.1567-1364.2008.00371.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
Commercial brewing yeast strains are exposed to a number of potential stresses including oxidative stress. The aim of this investigation was to measure the physiological and transcriptional changes of yeast cells during full-scale industrial brewing processes with a view to determining the environmental factors influencing the cell's oxidative stress response. Cellular antioxidant levels and genome-wide transcriptional changes were monitored throughout an industrial propagation and fermentation. The greatest increase in cellular antioxidants and transcription of antioxidant-encoding genes occurred as the rapidly fermentable sugars glucose and fructose were depleted from the growth medium (wort) and the cell population entered the stationary phase. The data suggest that, contrary to expectation, the oxidative stress response is not influenced by changes in the dissolved oxygen concentration of wort but is initiated as part of a general stress response to growth-limiting conditions, even in the absence of oxygen. A mechanism is proposed to explain the changes in antioxidant response observed in yeast during anaerobic fermentation. The available data suggest that the yeast cell does not experience oxidative stress during industrial brewery handling. This information may be taken into consideration when setting parameters for industrial brewery fermentation.
引用
收藏
页码:574 / 585
页数:12
相关论文
共 64 条
[1]  
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]   Effect of Cu,Zn superoxide dismutase disruption mutation on replicative senescence in Saccharomyces cerevisiae [J].
Barker, MG ;
Brimage, LJE ;
Smart, KA .
FEMS MICROBIOLOGY LETTERS, 1999, 177 (02) :199-204
[3]   CONTROL OF SACCHAROMYCES-CEREVISIAE CATALASE T-GENE (CTT1) EXPRESSION BY NUTRIENT SUPPLY VIA THE RAS-CYCLIC AMP PATHWAY [J].
BISSINGER, PH ;
WIESER, R ;
HAMILTON, B ;
RUIS, H .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (03) :1309-1315
[4]   HSP82 IS AN ESSENTIAL PROTEIN THAT IS REQUIRED IN HIGHER CONCENTRATIONS FOR GROWTH OF CELLS AT HIGHER TEMPERATURES [J].
BORKOVICH, KA ;
FARRELLY, FW ;
FINKELSTEIN, DB ;
TAULIEN, J ;
LINDQUIST, S .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (09) :3919-3930
[5]   Msn2p and Msn4p control a large number of genes induced at the diauxic transition which are repressed by cyclic AMP in Saccharomyces cerevisiae [J].
Boy-Marcotte, E ;
Perrot, M ;
Bussereau, F ;
Boucherie, H ;
Jacquet, M .
JOURNAL OF BACTERIOLOGY, 1998, 180 (05) :1044-1052
[6]  
Briggs D.E., 2004, BREWING SCI PRACTICE
[7]   The stress response is repressed during fermentation in brewery strains of yeast [J].
Brosnan, MP ;
Donnelly, D ;
James, TC ;
Bond, U .
JOURNAL OF APPLIED MICROBIOLOGY, 2000, 88 (05) :746-755
[8]  
Cabiscol E, 2000, J BIOL CHEM, V275, P27393
[9]   SYNTHESIS OF SUPEROXIDE-DISMUTASE, CATALASE AND OTHER ENZYMES AND OXYGEN AND SUPEROXIDE TOXICITY DURING CHANGES IN OXYGEN CONCENTRATION IN CULTURES OF BREWING YEAST [J].
CLARKSON, SP ;
LARGE, PJ ;
BOULTON, CA ;
BAMFORTH, CW .
YEAST, 1991, 7 (02) :91-103
[10]   Mitochondrial superoxide dismutase is essential for ethanol tolerance of Saccharomyces cerevisiae in the post-diauxic phase [J].
Costa, V ;
Amorim, MA ;
Reis, E ;
Quintanilha, A ;
MoradasFerreira, P .
MICROBIOLOGY-UK, 1997, 143 :1649-1656