EFFECT OF YEAST FUMARASE GENE (FUM1) DISRUPTION ON PRODUCTION OF MALIC, FUMARIC AND SUCCINIC ACIDS IN SAKE MASH

被引:22
作者
MAGARIFUCHI, T
GOTO, K
IIMURA, Y
TADENUMA, M
TAMURA, G
机构
[1] RES INST BREWING RESOURCES CO LTD, KITA KU, TOKYO 114, JAPAN
[2] NATL RES INST BREWING, KITA KU, TOKYO 114, JAPAN
来源
JOURNAL OF FERMENTATION AND BIOENGINEERING | 1995年 / 80卷 / 04期
关键词
SACCHAROMYCES CEREVISIAE; FUMARASE; FUM1; GENE; GENE DISRUPTION; SAKE; ORGANIC ACID;
D O I
10.1016/0922-338X(95)94204-5
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
Organic acids are essential flavor components in alcoholic beverages such as wine and sake (Japanese rice wine). The effects of fumarase deficiency on the productivity of malic, fumaric and succinic acids in Saccharomyces cerevisiae were examined using the FUM1 gene disruptant. The single nuclear gene FUM1 encoding fumarase in S. cerevisiae, DBY746, was disrupted by a site-directed one-step gene disruption technique. The fumarase activity of the isolated FUM1 disruptant was abolished. The FUM1 disruptant having a pet phenotype showed no growth on minimal medium containing glycerol as a carbon source even after prolonged incubation. The productions of organic acids by the FUM1 disruptant in YPD liquid culture containing 10% glucose and in sake mash were analyzed by HPLC. The analytical results of the FUM1 disruptant showed there were no differences in extracellular malate productivity, fumarate productivity had increased, and that succinate productivity was reduced compared with those of the control strain. In the production of sake using the FUM1 disruptant, fermentation ability as monitored by CO2 evolution was not different from that of the control strain. These results indicate that site-directed FUM1 disruption alters organic acid production without any loss of fermentation ability in yeast.
引用
收藏
页码:355 / 361
页数:7
相关论文
共 35 条
[1]  
AIKAWA M, 1992, HAKKOKOGAKU KAISHI, V70, P473
[2]   STERILE HOST YEASTS (SHY) - EUKARYOTIC SYSTEM OF BIOLOGICAL CONTAINMENT FOR RECOMBINANT DNA EXPERIMENTS [J].
BOTSTEIN, D ;
FALCO, SC ;
STEWART, SE ;
BRENNAN, M ;
SCHERER, S ;
STINCHCOMB, DT ;
STRUHL, K ;
DAVIS, RW .
GENE, 1979, 8 (01) :17-24
[3]   KINETICS OF ENZYME CHANGES IN YEAST UNDER CONDITIONS THAT CAUSE LOSS OF MITOCHONDRIA [J].
CHAPMAN, C ;
BARTLEY, W .
BIOCHEMICAL JOURNAL, 1968, 107 (04) :455-&
[4]  
CUPP JR, 1992, J BIOL CHEM, V267, P16417
[5]  
CUPP JR, 1991, J BIOL CHEM, V266, P22199
[6]  
DUNTZE W, 1969, EUR J BIOCHEM, V10, P83
[7]   MOLECULAR-CLONING OF THE YEAST MITOCHONDRIAL ACONITASE GENE (ACO1) AND EVIDENCE OF A SYNERGISTIC REGULATION OF EXPRESSION BY GLUCOSE PLUS GLUTAMATE [J].
GANGLOFF, SP ;
MARGUET, D ;
LAUQUIN, GJM .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (07) :3551-3561
[8]   ACTIVITY AND REGULATION OF ANAPLEROTIC AND GLUCONEOGENETIC ENZYMES DURING GROWTH PROCESS OF BAKERS-YEAST - BIPHASIC GROWTH [J].
HAARASILTA, S ;
OURA, E .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1975, 52 (01) :1-7
[9]   STUDIES ON TRANSFORMATION OF ESCHERICHIA-COLI WITH PLASMIDS [J].
HANAHAN, D .
JOURNAL OF MOLECULAR BIOLOGY, 1983, 166 (04) :557-580
[10]   STUDIES ON SUCCINATE DEHYDROGENASE .14. INTRACELLULAR DISTRIBUTION CATALYTIC PROPERTIES AND REGULATION OF FUMARATE REDUCTASES IN YEAST [J].
HAUBER, J ;
SINGER, TP .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1967, 3 (01) :105-&