Comparative metabolomic analysis on industrial continuous and batch ethanol fermentation processes by GC-TOF-MS

被引:66
作者
Ding, Ming-Zhu [1 ]
Cheng, Jing-Sheng [1 ]
Xiao, Wen-Hai [1 ]
Qiao, Bin [1 ]
Yuan, Ying-Jin [1 ]
机构
[1] Tianjin Univ, Key Lab Syst Bioengn, Minist Educ, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
Metabolic profiles; GC-TOF-MS; Continuous fermentation; Batch fermentation; S; cerevisiae; CHROMATOGRAPHY-MASS SPECTROMETRY; SIGNAL-TRANSDUCTION PATHWAY; SACCHAROMYCES-CEREVISIAE; FUNCTIONAL GENOMICS; PROTEOMIC ANALYSIS; STRESS-RESPONSE; WINE STRAIN; YEAST; IDENTIFICATION; METABONOMICS;
D O I
10.1007/s11306-008-0145-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The intracellular metabolic profile characterization of Saccharomyces cerevisiae throughout industrial ethanol fermentation was investigated using gas chromatography coupled to time-of-flight mass spectrometry. A total of 143 and 128 intracellular metabolites in S. cerevisiae were detected and quantified in continuous and batch fermentations, respectively. The two fermentation processes were both clearly distinguished into three main phases by principal components analysis. Furthermore, the levels of some metabolites involved in central carbon metabolism varied significantly throughout both processes. Glycerol and phosphoric acid were principally responsible for discriminating seed, main and final phases of continuous fermentation, while lactic acid and glycerol contributed mostly to telling different phases of batch fermentation. In addition, the levels of some amino acids such as glycine varied significantly during both processes. These findings provide new insights into the metabolomic characteristics during industrial ethanol fermentation processes.
引用
收藏
页码:229 / 238
页数:10
相关论文
共 41 条
[1]  
ABRAMS R, 1948, J BIOL CHEM, V173, P429
[2]   Functional genomic analysis of a commercial wine strain of Saccharomyces cerevisiae under differing nitrogen conditions [J].
Backhus, Leilah E. ;
DeRisi, Joseph ;
Brown, Patrick O. ;
Bisson, Linda F. .
FEMS YEAST RESEARCH, 2001, 1 (02) :111-125
[3]   ROLES OF GLYCEROL AND GLYCEROL-3-PHOSPHATE DEHYDROGENASE (NAD+) IN ACQUIRED OSMOTOLERANCE OF SACCHAROMYCES-CEREVISIAE [J].
BLOMBERG, A ;
ADLER, L .
JOURNAL OF BACTERIOLOGY, 1989, 171 (02) :1087-1092
[4]   PHYSIOLOGY OF OSMOTOLERANCE IN FUNGI [J].
BLOMBERG, A ;
ADLER, L .
ADVANCES IN MICROBIAL PHYSIOLOGY, 1992, 33 :145-212
[5]   Identification of genes and proteins induced during the lag and early exponential phase of lager brewing yeasts [J].
Brejning, J ;
Arneborg, N ;
Jespersen, L .
JOURNAL OF APPLIED MICROBIOLOGY, 2005, 98 (02) :261-271
[6]   AN OSMOSENSING SIGNAL TRANSDUCTION PATHWAY IN YEAST [J].
BREWSTER, JL ;
DEVALOIR, T ;
DWYER, ND ;
WINTER, E ;
GUSTIN, MC .
SCIENCE, 1993, 259 (5102) :1760-1763
[7]   Manifold anomalies in gene expression in a vineyard isolate of Saccharomyces cerevisiae revealed by DNA microarray analysis [J].
Cavalieri, D ;
Townsend, JP ;
Hartl, DL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (22) :12369-12374
[8]   Comparative proteome analysis of robust Saccharomyces cerevisiae insights into industrial continuous and batch fermentation [J].
Cheng, Jing-Sheng ;
Qiao, Bin ;
Yuan, Ying-Jin .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2008, 81 (02) :327-338
[9]  
DAVENPORT KR, 1995, J BIOL CHEM, V270, P30157
[10]   Metabolite profiling for analysis of yeast stress response during very high gravity ethanol fermentations [J].
Devantier, R ;
Scheithauer, B ;
Villas-Bôas, SG ;
Pedersen, S ;
Olsson, L .
BIOTECHNOLOGY AND BIOENGINEERING, 2005, 90 (06) :703-714