Mutation of the ptsC gene results in increased production of succinate in fermentation of glucose by Escherichia coli

被引:171
作者
Chatterjee, R
Millard, CS
Champion, K
Clark, DP
Donnelly, MI
机构
[1] Argonne Natl Lab, Div Environm Res, Argonne, IL 60439 USA
[2] So Illinois Univ, Dept Microbiol, Carbondale, IL 62901 USA
关键词
D O I
10.1128/AEM.67.1.148-154.2001
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
Escherichia coli NZN111 is blocked in the ability to grow fermentatively on glucose but gave rise spontaneously to a mutant that had this ability. The mutant carries out a balanced fermentation of glucose to give approximately 1 mol of succinate, 0.5 mol of acetate, and 0.5 mol of ethanol per mol of glucose. The causative mutation was mapped to the ptsG gene, which encodes the membrane-hound, glucose-specific permease of the phosphotransferase system, protein EIICBglc. Replacement of the chromosomal ptsG gene with an insertionally inactivated form also restored growth on glucose and resulted in the same distribution of fermentation products. The physiological characteristics of the spontaneous and null mutants were consistent with loss of function of the ptsG gene product; the mutants possessed greatly reduced glucose phosphotransferase activity and lacked normal glucose repression. Introduction of the null mutant into strains not blocked in the ability to ferment glucose also increased succinate production in those strains. This phenomenon was widespread, occurring in different lineages off. coli, including E. coli B.
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页码:148 / 154
页数:7
相关论文
共 34 条
[1]  
[Anonymous], 1996, Escherichia coli and Salmonella typhimurium: Cellular and Molecular Biology
[2]  
[Anonymous], ENZYMES
[3]   NEW APPROACH TO CULTIVATION OF METHANOGENIC BACTERIA - 2-MERCAPTOETHANESULFONIC ACID (HS-COM)-DEPENDENT GROWTH OF METHANOBACTERIUM-RUMINANTIUM IN A PRESSURIZED ATMOSPHERE [J].
BALCH, WE ;
WOLFE, RS .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1976, 32 (06) :781-791
[4]   DISSIMILATION OF GLUCOSE AT CONTROLLED PH VALUES BY PIGMENTED AND NON-PIGMENTED STRAINS OF ESCHERICHIA-COLI [J].
BLACKWOOD, AC ;
NEISH, AC ;
LEDINGHAM, GA .
JOURNAL OF BACTERIOLOGY, 1956, 72 (04) :497-499
[5]  
Bock A., 1996, ESCHERICHIA COLI SAL, V1, P262
[6]   II-BGLC, A GLUCOSE RECEPTOR OF THE BACTERIAL PHOSPHOTRANSFERASE SYSTEM - MOLECULAR-CLONING OF PTSG AND PURIFICATION OF THE RECEPTOR FROM AN OVERPRODUCING STRAIN OF ESCHERICHIA-COLI [J].
BOUMA, CL ;
MEADOW, ND ;
STOVER, EW ;
ROSEMAN, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (04) :930-934
[7]   The IdhA gene encoding the fermentative lactate dehydrogenase of Escherichia coli [J].
Bunch, PK ;
MatJan, F ;
Lee, N ;
Clark, DP .
MICROBIOLOGY-UK, 1997, 143 :187-195
[8]   Metabolic consequences of phosphotransferase (PTS) mutation in a phenylalanine-producing recombinant Escherichia coli [J].
Chen, RZ ;
Hatzimanikatis, V ;
Yap, WMGJ ;
Postma, PW ;
Bailey, JE .
BIOTECHNOLOGY PROGRESS, 1997, 13 (06) :768-775
[9]   THE FERMENTATION PATHWAYS OF ESCHERICHIA-COLI [J].
CLARK, DP .
FEMS MICROBIOLOGY LETTERS, 1989, 63 (03) :223-234
[10]   POSITIVE REGULATION OF THE PTS OPERON OF ESCHERICHIA-COLI - GENETIC-EVIDENCE FOR A SIGNAL TRANSDUCTION MECHANISM [J].
DEREUSE, H ;
DANCHIN, A .
JOURNAL OF BACTERIOLOGY, 1991, 173 (02) :727-733