Literature DB >> 18609599

Metabolic flux distributions in Corynebacterium glutamicum during growth and lysine overproduction.

J J Vallino1, G Stephanopoulos.   

Abstract

The two main contributions of this are the solidification of Corynebacterium glutamicum biochemistry guided by bioreaction network analysis, and the determination of bansal metabolic flux distributions during growth and lysine synthesis. Employed methodology makes use of stoichiometrically based mass balances to determine flux distributions in the C. glutamicum metabolic network. Presented are a brief description of the methodology, a through literature review of glutamic acid bacteria biochemistry, and specific results obtained through a combination of fermentation studies and analysis-directed intracellular assays. The latter include the findings of the lack of activity of glyoxylate shunt, and that phosphoenolpyruvate carboxylase (PPC) is the only anaplerotic reaction expressed in C. glutamicum cultivated on glucose minimal media. Network simplifications afforded by the above findings facilitated the determination of metabolic flux distributions under a variety of culture conditions and led to the following conclusions. Both the pentose phosphate pathway and PPC support fluxes during growth and lysine overproduction branch point does not appear to limit lysine synthesis. (c) 1993 John Wiley & Sons, Inc.

Entities:  

Year:  1993        PMID: 18609599     DOI: 10.1002/bit.260410606

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  59 in total

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6.  Metabolic fluxes in Corynebacterium glutamicum during lysine production with sucrose as carbon source.

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9.  Osmotic stress response: quantification of cell maintenance and metabolic fluxes in a lysine-overproducing strain of Corynebacterium glutamicum.

Authors:  Cristian A Varela; Mauricio E Baez; Eduardo Agosin
Journal:  Appl Environ Microbiol       Date:  2004-07       Impact factor: 4.792

10.  NMR method for measuring carbon-13 isotopic enrichment of metabolites in complex solutions.

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