This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Novák, L.
Right arrow Articles by Loubiere, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Novák, L.
Right arrow Articles by Loubiere, P.

 Previous Article  |  Next Article 

Journal of Bacteriology, February 2000, p. 1136-1143, Vol. 182, No. 4
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.

The Metabolic Network of Lactococcus lactis: Distribution of 14C-Labeled Substrates between Catabolic and Anabolic Pathways

L. Novák and P. Loubiere*

Centre de Bioingénierie Gilbert Durand, UMR CNRS 5504, UR 792 INRA, Institut National des Sciences Appliquées, Complexe Scientifique de Rangueil, F-31077 Toulouse Cedex 4, France

Received 22 April 1999/Accepted 22 November 1999

Lactococcus lactis NCDO 2118 was grown in a simple synthetic medium containing only six essential amino acids and glucose as carbon substrates to determine qualitatively and quantitatively the carbon fluxes into the metabolic network. The specific rates of substrate consumption, product formation, and biomass synthesis, calculated during the exponential growth phase, represented the carbon fluxes within the catabolic and anabolic pathways. The macromolecular composition of the biomass was measured to distribute the global anabolic flux into the specific anabolic pathways. Finally, the distribution of radiolabeled substrates, both into the excreted fermentation end products and into the different macromolecular fractions of biomass, was monitored. The classical end products of lactic acid metabolism (lactate, formate, and acetate) were labeled with glucose, which did not label other excreted products, and to a lesser extent with serine, which was deaminated to pyruvate and represented approximately 10% of the pyruvate flux. Other minor products, keto and hydroxy acids, were produced from glutamate and branched-chain amino acids via deamination and subsequent decarboxylation and/or reduction. Glucose labeled all biomass fractions and accounted for 66% of the cellular carbon, although this represented only 5% of the consumed glucose.


* Corresponding author. Mailing address: INSA, Département de Génie Biochimique et Alimentaire, 135 Ave. de Rangueil, F-31077 Toulouse Cedex 4, France. Phone: (33) 5 61 55 94 38. Fax: (33) 5 61 55 94 02. E-mail: loubiere{at}insa-tlse.fr.


Journal of Bacteriology, February 2000, p. 1136-1143, Vol. 182, No. 4
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Teusink, B., Wiersma, A., Molenaar, D., Francke, C., de Vos, W. M., Siezen, R. J., Smid, E. J. (2006). Analysis of Growth of Lactobacillus plantarum WCFS1 on a Complex Medium Using a Genome-scale Metabolic Model. J. Biol. Chem. 281: 40041-40048 [Abstract] [Full Text]  
  • Raynaud, S., Perrin, R., Cocaign-Bousquet, M., Loubiere, P. (2005). Metabolic and Transcriptomic Adaptation of Lactococcus lactis subsp. lactis Biovar diacetylactis in Response to Autoacidification and Temperature Downshift in Skim Milk. Appl. Environ. Microbiol. 71: 8016-8023 [Abstract] [Full Text]  
  • Goffman, F. D., Alonso, A. P., Schwender, J., Shachar-Hill, Y., Ohlrogge, J. B. (2005). Light Enables a Very High Efficiency of Carbon Storage in Developing Embryos of Rapeseed. Plant Physiol. 138: 2269-2279 [Abstract] [Full Text]  
  • Netzer, R., Peters-Wendisch, P., Eggeling, L., Sahm, H. (2004). Cometabolism of a Nongrowth Substrate: L-Serine Utilization by Corynebacterium glutamicum. Appl. Environ. Microbiol. 70: 7148-7155 [Abstract] [Full Text]  
  • Palmfeldt, J., Paese, M., Hahn-Hagerdal, B., van Niel, E. W. J. (2004). The Pool of ADP and ATP Regulates Anaerobic Product Formation in Resting Cells of Lactococcus lactis. Appl. Environ. Microbiol. 70: 5477-5484 [Abstract] [Full Text]  
  • Vido, K., le Bars, D., Mistou, M.-Y., Anglade, P., Gruss, A., Gaudu, P. (2004). Proteome Analyses of Heme-Dependent Respiration in Lactococcus lactis: Involvement of the Proteolytic System. J. Bacteriol. 186: 1648-1657 [Abstract] [Full Text]  
  • Nordkvist, M., Jensen, N. B. S., Villadsen, J. (2003). Glucose Metabolism in Lactococcus lactis MG1363 under Different Aeration Conditions: Requirement of Acetate To Sustain Growth under Microaerobic Conditions. Appl. Environ. Microbiol. 69: 3462-3468 [Abstract] [Full Text]  
  • Neves, A. R., Ventura, R., Mansour, N., Shearman, C., Gasson, M. J., Maycock, C., Ramos, A., Santos, H. (2002). Is the Glycolytic Flux in Lactococcus lactis Primarily Controlled by the Redox Charge? KINETICS OF NAD+ AND NADH POOLS DETERMINED IN VIVO BY 13C NMR. J. Biol. Chem. 277: 28088-28098 [Abstract] [Full Text]  
  • Andersen, H. W., Solem, C., Hammer, K., Jensen, P. R. (2001). Twofold Reduction of Phosphofructokinase Activity in Lactococcus lactis Results in Strong Decreases in Growth Rate and in Glycolytic Flux. J. Bacteriol. 183: 3458-3467 [Abstract] [Full Text]