DNA microarray analysis on Saccharomyces cerevisiae under high carbon dioxide concentration in fermentation process

被引:0
作者
Nagahisa, K
Nakajima, T
Yoshikawa, K
Hirasawa, T
Katakura, Y
Furusawa, C
Shioya, S
Shimizu, H
机构
[1] Osaka Univ, Grad Sch Informat Sci & Technol, Dept Bioinformat Engn, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Engn, Dept Biotechnol, Suita, Osaka 5650871, Japan
关键词
carbon dioxide; Saccharomyces cerevisiae; transcriptome; growth inhibition; ALD6;
D O I
暂无
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
The effect of carbon dioxide on yeast growth was investigated during the cultivation of pH 5.0 and pH 6.8, by replacing the nitrogen part with carbon dioxide under aerobic conditions. The values of the specific growth rate under pH 5.0 and pH 6.8 conditions became 64.0% and 46.9%, respectively, compared to those before the change in gas composition. This suggests that the effect of carbon dioxide was greater pronounced in pH 6.8 than in pH 5.0. The genome-wide transcriptional response to elevated carbon dioxide was examined using a DNA microarray. As for upregulated genes, it was noteworthy that 3 genes were induced upon entry into a stationary phase and 6 genes were involved in stress response. Of 53 downregulated genes, 22 genes were involved in the ribosomal biogenesis and assembly and 5 genes were involved in the lipid metabolism. These facts suggest that carbon dioxide could bring the cell conditions partially to a stationary phase. The ALD6 gene encoding for cytosolic acetalclehyde dehydrogenase was downregulated, which would lead to a lack of cell components for the growth. The downregulation of ALD6 was greater in pH 6.8 than in pH 5.0, consistent with physiological response. This suggests that it might be the most effective factor for growth inhibition.
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收藏
页码:451 / 461
页数:11
相关论文
共 38 条
[1]   CARBON-DIOXIDE INHIBITION OF YEAST GROWTH IN BIOMASS PRODUCTION [J].
CHEN, SL ;
GUTMANIS, F .
BIOTECHNOLOGY AND BIOENGINEERING, 1976, 18 (10) :1455-1462
[2]   SGD:: Saccharomyces Genome Database [J].
Cherry, JM ;
Adler, C ;
Ball, C ;
Chervitz, SA ;
Dwight, SS ;
Hester, ET ;
Jia, YK ;
Juvik, G ;
Roe, T ;
Schroeder, M ;
Weng, SA ;
Botstein, D .
NUCLEIC ACIDS RESEARCH, 1998, 26 (01) :73-79
[3]   FUNCTIONAL-STUDIES OF YEAST GLUCOKINASE [J].
CLIFTON, D ;
WALSH, RB ;
FRAENKEL, DG .
JOURNAL OF BACTERIOLOGY, 1993, 175 (11) :3289-3294
[4]   Expression of a glutamate decarboxylase homologue is required for normal oxidative stress tolerance in Saccharomyces cerevisiae [J].
Coleman, ST ;
Fang, TK ;
Rovinsky, SA ;
Turano, FJ ;
Moye-Rowley, WS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (01) :244-250
[5]   IDENTIFICATION AND CHARACTERIZATION OF A NOVEL YEAST GENE - THE YGP1 GENE-PRODUCT IS A HIGHLY GLYCOSYLATED SECRETED PROTEIN THAT IS SYNTHESIZED IN RESPONSE TO NUTRIENT LIMITATION [J].
DESTRUELLE, M ;
HOLZER, H ;
KLIONSKY, DJ .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (04) :2740-2754
[6]  
Donalies UEB, 2001, CURR GENET, V39, P150
[7]  
Estruch F, 2000, FEMS MICROBIOL REV, V24, P469, DOI 10.1016/S0168-6445(00)00035-8
[8]   Life with 6000 genes [J].
Goffeau, A ;
Barrell, BG ;
Bussey, H ;
Davis, RW ;
Dujon, B ;
Feldmann, H ;
Galibert, F ;
Hoheisel, JD ;
Jacq, C ;
Johnston, M ;
Louis, EJ ;
Mewes, HW ;
Murakami, Y ;
Philippsen, P ;
Tettelin, H ;
Oliver, SG .
SCIENCE, 1996, 274 (5287) :546-&
[9]  
HIRASAWA T, 2005, IN PRESS APPL MICROB
[10]   CLONING AND CHARACTERIZATION OF 7 CDNAS FOR HYPEROSMOLARITY-RESPONSIVE (HOR) GENES OF SACCHAROMYCES-CEREVISIAE [J].
HIRAYAMA, T ;
MAEDA, T ;
SAITO, H ;
SHINOZAKI, K .
MOLECULAR AND GENERAL GENETICS, 1995, 249 (02) :127-138