Medium Optimization for Improved Ethanol Production in Very High Gravity Fermentation

被引:3
作者
Hu Chunkeng [1 ]
Qin Qing [1 ]
Gao Peipei [1 ]
机构
[1] Huaqiao Univ, Dept Biol Engn, Sch Chem Engn, Xiamen 361021, Peoples R China
关键词
medium optimization; very high gravity fermentation; trehalose; plasma membrane ATPase; MEMBRANE H+-ATPASE; FUEL ALCOHOL PRODUCTION; SACCHAROMYCES-CEREVISIAE; MAXIMAL TOLERANCE; SUPPLEMENTATION; STRESS; IDENTIFICATION; ACTIVATION; TREHALOSE; YEASTS;
D O I
暂无
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
An optimal medium (300 g.L(-1) initial glucose) comprising 6.3 mmol.L(-1) Mg(2+), 5.0 mmol.L(-1) Ca(2+), 15.0 g.L(-1) peptone and 21.5 g.L(-1) yeast extract was determined by uniform design to improve very high gravity (VHG) ethanol fermentation, showing over 30% increase in final ethanol (from 13.1% to 17.1%, by volume), 29% decrease in fermentation time (from 84 to 60 h), 80% increase in biomass formation and 26% increase in glucose utilization. Experiments also revealed physiological aspects linked to the fermentation enhancements. Compared to the control, trehalose in the cells grown in optimal fermentation medium increased 17.9-, 2.8-, 1.9-, 1.8- and 1.9-fold at the fermentation time of 12, 24, 36, 48 and 60 h, respectively. Its sharp rise at the early stage of fermentation when there was a considerable osmotic stress suggested that trehalose played an important role in promoting fermentation. Meanwhile, at the identical five fermentation time, the plasma membrane ATPase activity of the cells grown in optimal medium was 2.3, 1.8, 1.6, 1.5 and 1.3 times that of the control, respectively. Their disparities in enzymatic activity became wider when the glucose levels were dramatically changed for ethanol production, suggesting this enzyme also contributed to the fermentation improvements. Thus, medium optimization for VHG ethanol fermentation was found to trigger the increased yeast trehalose accumulation and plasma membrane ATPase activity.
引用
收藏
页码:1017 / 1022
页数:6
相关论文
共 26 条
[1]   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
[2]   Improvement of very high gravity ethanol fermentation by media supplementation using Saccharomyces cerevisiae [J].
Bafrncová, P ;
Smogrovicová, D ;
Sláviková, I ;
Pátková, J ;
Dömény, Z .
BIOTECHNOLOGY LETTERS, 1999, 21 (04) :337-341
[3]   Ethanol fermentation technologies from sugar and starch feedstocks [J].
Bai, F. W. ;
Anderson, W. A. ;
Moo-Young, M. .
BIOTECHNOLOGY ADVANCES, 2008, 26 (01) :89-105
[4]   Trehalose promotes the survival of Saccharomyces cerevisiae during lethal ethanol stress, but does not influence growth under sublethal ethanol stress [J].
Bandara, Ajith ;
Fraser, Sarah ;
Chambers, Paul J. ;
Stanley, Grant A. .
FEMS YEAST RESEARCH, 2009, 9 (08) :1208-1216
[5]   Application of multistage continuous fermentation for production of fuel alcohol by very-high-gravity fermentation technology [J].
Bayrock, DP ;
Ingledew, WM .
JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY, 2001, 27 (02) :87-93
[6]   Protective agents used to reverse the metabolic changes induced in wine yeasts by concomitant osmotic and thermal stress [J].
Caridi, A .
LETTERS IN APPLIED MICROBIOLOGY, 2002, 35 (02) :98-101
[7]   The natural osmolyte trehalose is a positive regulator of the heat-induced activity of yeast heat shock transcription factor [J].
Conlin, Laura K. ;
Nelson, Hillary C. M. .
MOLECULAR AND CELLULAR BIOLOGY, 2007, 27 (04) :1505-1515
[8]   Regulation of yeast H+-ATPase by protein kinases belonging to a family dedicated to activation of plasma membrane transporters [J].
Goossens, A ;
de la Fuente, N ;
Forment, J ;
Serrano, R ;
Portillo, F .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (20) :7654-7661
[9]   Osmotic stress signaling and osmoadaptation in Yeasts [J].
Hohmann, S .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2002, 66 (02) :300-+
[10]  
Hu Chun-Keng, 2003, Chinese Journal of Biotechnology, V19, P715