Quantitative determination of metabolic fluxes during coutilization of two carbon sources: Comparative analyses with corynebacterium glutamicum during growth on acetate and/or glucose

被引:208
作者
Wendisch, VF [1 ]
De Graaf, AA [1 ]
Sahm, H [1 ]
Eikmanns, BJ [1 ]
机构
[1] Res Ctr, Inst Biotechnol 1, D-52428 Julich, Germany
关键词
D O I
10.1128/JB.182.11.3088-3096.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Growth of Corynebacterium glutamicum on mixtures of the carbon sources glucose and acetate is shown to be distinct from growth on either substrate alone. The organism showed nondiauxic growth on media containing acetate-glucose mixtures and simultaneously metabolized these substrates. Compared to those for growth on acetate or glucose alone, the consumption rates of the individual substrates were reduced during acetate-glucose cometabolism, resulting in similar total carbon consumption rates for the three conditions. By C-13-labeling experiments with subsequent nuclear magnetic resonance analyses in combination with metabolite balancing, the in vivo activities for pathways or single enzymes in the central metabolism of C. glatamicum were quantified for growth on acetate, on glucose, and on both carbon sources. The activity of the citric acid cycle was high on acetate, intermediate on acetate plus glucose, and low on glucose, corresponding to in vivo activities of citrate synthase of 413, 219, and 111 nmol (mg of protein)(-1) min(-1), respectively. The citric acid cycle was replenished by carboxylation of phosphoenolpyruvate (PEP) and/or pyruvate (30 nmol [mg of protein](-1) min(-1)) during growth on glucose. Although levels of PEP carboxylase and pyruvate carboxylase during growth on acetate were similar to those for growth on glucose, anaplerosis occurred solely by the glyoxylate cycle (99 nmol [mg of protein](-1) min(-1)). Surprisingly, the anaplerotic function was fulfilled completely by the glyoxylate cycle (50 nmol [mg of protein](-1) min(-1)) on glucose plus acetate also. Consistent with the predictions deduced from the metabolic flux analyses, a glyoxylate cycle-deficient mutant of C. glutamicum, constructed by targeted deletion of the isocitrate lyase and malate synthase genes, exhibited impaired growth on acetate-glucose mixtures.
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页码:3088 / 3096
页数:9
相关论文
共 60 条
[41]   GROWTH AND ENERGETICS OF LEUCONOSTOC-OENOS DURING COMETABOLISM OF GLUCOSE WITH CITRATE OR FRUCTOSE [J].
SALOU, P ;
LOUBIERE, P ;
PAREILLEUX, A .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1994, 60 (05) :1459-1466
[42]  
Sambrook J., 1989, MOL CLONING
[43]   SMALL MOBILIZABLE MULTIPURPOSE CLONING VECTORS DERIVED FROM THE ESCHERICHIA-COLI PLASMIDS PK18 AND PK19 - SELECTION OF DEFINED DELETIONS IN THE CHROMOSOME OF CORYNEBACTERIUM-GLUTAMICUM [J].
SCHAFER, A ;
TAUCH, A ;
JAGER, W ;
KALINOWSKI, J ;
THIERBACH, G ;
PUHLER, A .
GENE, 1994, 145 (01) :69-73
[44]   A FUNCTIONALLY SPLIT PATHWAY FOR LYSINE SYNTHESIS IN CORYNEBACTERIUM-GLUTAMICUM [J].
SCHRUMPF, B ;
SCHWARZER, A ;
KALINOWSKI, J ;
PUHLER, A ;
EGGELING, L ;
SAHM, H .
JOURNAL OF BACTERIOLOGY, 1991, 173 (14) :4510-4516
[45]   C-13 AS A LABEL IN BIOSYNTHETIC STUDIES/DIES [J].
SEQUIN, U ;
SCOTT, AI .
SCIENCE, 1974, 186 (4159) :101-107
[46]   QUANTITATIVE IN-VIVO NUCLEAR-MAGNETIC-RESONANCE STUDIES OF HYBRIDOMA METABOLISM [J].
SHARFSTEIN, ST ;
TUCKER, SN ;
MANCUSO, A ;
BLANCH, HW ;
CLARK, DS .
BIOTECHNOLOGY AND BIOENGINEERING, 1994, 43 (11) :1059-1074
[47]  
Sonntag K, 1995, APPL MICROBIOL BIOT, V44, P489, DOI 10.1007/s002530050587
[48]  
SONNTAG K, 1995, EUR J BIOCHEM, V213, P1325
[49]   NETWORK RIGIDITY AND METABOLIC ENGINEERING IN METABOLITE OVERPRODUCTION [J].
STEPHANOPOULOS, G ;
VALLINO, JJ .
SCIENCE, 1991, 252 (5013) :1675-1681
[50]   BIOSYNTHETICALLY DIRECTED FRACTIONAL C-13-LABELING OF PROTEINOGENIC AMINO-ACIDS - AN EFFICIENT ANALYTICAL TOOL TO INVESTIGATE INTERMEDIARY METABOLISM [J].
SZYPERSKI, T .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 232 (02) :433-448