Document Detail


Quantitative determination of metabolic fluxes during coutilization of two carbon sources: comparative analyses with Corynebacterium glutamicum during growth on acetate and/or glucose.
MedLine Citation:
PMID:  10809686     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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 (13)C-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. glutamicum 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.
Authors:
V F Wendisch; A A de Graaf; H Sahm; B J Eikmanns
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of bacteriology     Volume:  182     ISSN:  0021-9193     ISO Abbreviation:  J. Bacteriol.     Publication Date:  2000 Jun 
Date Detail:
Created Date:  2000-06-05     Completed Date:  2000-06-05     Revised Date:  2013-04-17    
Medline Journal Info:
Nlm Unique ID:  2985120R     Medline TA:  J Bacteriol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  3088-96     Citation Subset:  IM    
Affiliation:
Institute of Biotechnology 1, Research Center Jülich, Germany. v.wendisch@fz-juelich.de
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MeSH Terms
Descriptor/Qualifier:
Acetates / metabolism*
Carbon Isotopes
Citric Acid Cycle
Corynebacterium / growth & development,  metabolism*
Glucose / metabolism*
Glyceric Acids / metabolism
Glyoxylates / metabolism
Ketoglutaric Acids / metabolism
Models, Biological
Nuclear Magnetic Resonance, Biomolecular
Oxaloacetic Acid / metabolism
Pyruvic Acid / metabolism
Chemical
Reg. No./Substance:
0/Acetates; 0/Carbon Isotopes; 0/Glyceric Acids; 0/Glyoxylates; 0/Ketoglutaric Acids; 127-17-3/Pyruvic Acid; 328-42-7/Oxaloacetic Acid; 328-50-7/alpha-ketoglutaric acid; 50-99-7/Glucose; 820-11-1/3-phosphoglycerate; JQ39C92HH6/glyoxylic acid
Comments/Corrections

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