Literature DB >> 10699864

Metabolic flux distributions in Corynebacterium glutamicum during growth and lysine overproduction. Reprinted from Biotechnology and Bioengineering, Vol. 41, Pp 633-646 (1993).

J J Vallino, G Stephanopoulos.   

Abstract

The two main contributions of this article are the solidification of Corynebacterium glutamicum biochemistry guided by bioreaction network analysis, and the determination of basal 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 thorough 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 significant fluxes during growth and lysine overproduction, and that flux partitioning at the glucosa-6-phosphate branch point does not appear to limit lysine synthesis. Copyright 1993 John Wiley & Sons, Inc.

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Year:  2000        PMID: 10699864

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


  8 in total

1.  Genetic and functional analysis of the soluble oxaloacetate decarboxylase from Corynebacterium glutamicum.

Authors:  Simon Klaffl; Bernhard J Eikmanns
Journal:  J Bacteriol       Date:  2010-03-16       Impact factor: 3.490

2.  Double deletion of dtsR1 and pyc induce efficient L: -glutamate overproduction in Corynebacterium glutamicum.

Authors:  Wenjuan Yao; Xiaozhao Deng; Hui Zhong; Miao Liu; Pu Zheng; Zhihao Sun; Yun Zhang
Journal:  J Ind Microbiol Biotechnol       Date:  2009-05-02       Impact factor: 3.346

3.  Complex regulation of the phosphoenolpyruvate carboxykinase gene pck and characterization of its GntR-type regulator IolR as a repressor of myo-inositol utilization genes in Corynebacterium glutamicum.

Authors:  Simon Klaffl; Melanie Brocker; Jörn Kalinowski; Bernhard J Eikmanns; Michael Bott
Journal:  J Bacteriol       Date:  2013-07-19       Impact factor: 3.490

4.  A possibilistic framework for constraint-based metabolic flux analysis.

Authors:  Francisco Llaneras; Antonio Sala; Jesús Picó
Journal:  BMC Syst Biol       Date:  2009-07-31

5.  Development and experimental verification of a genome-scale metabolic model for Corynebacterium glutamicum.

Authors:  Yohei Shinfuku; Natee Sorpitiporn; Masahiro Sono; Chikara Furusawa; Takashi Hirasawa; Hiroshi Shimizu
Journal:  Microb Cell Fact       Date:  2009-08-03       Impact factor: 5.328

6.  The topology of metabolic isotope labeling networks.

Authors:  Michael Weitzel; Wolfgang Wiechert; Katharina Nöh
Journal:  BMC Bioinformatics       Date:  2007-08-29       Impact factor: 3.169

7.  Metabolic responses to pyruvate kinase deletion in lysine producing Corynebacterium glutamicum.

Authors:  Judith Becker; Corinna Klopprogge; Christoph Wittmann
Journal:  Microb Cell Fact       Date:  2008-03-13       Impact factor: 5.328

Review 8.  Quantification of Microbial Phenotypes.

Authors:  Verónica S Martínez; Jens O Krömer
Journal:  Metabolites       Date:  2016-12-09
  8 in total

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