Literature DB >> 15383716

Metabolic analysis of Corynebacterium glutamicum during lactate and succinate productions under oxygen deprivation conditions.

Masayuki Inui1, Shikiko Murakami, Shohei Okino, Hideo Kawaguchi, Alain A Vertès, Hideaki Yukawa.   

Abstract

Lactate and succinate were produced from glucose by Corynebacterium glutamicum under oxygen deprivation conditions without growth. Addition of bicarbonate to the reaction mixture led not only to a 3.6-fold increase in succinate production rate, but also to a 2.3- and 2.5-fold increase, respectively, of the rates of lactate production and glucose consumption, compared to the control. Furthermore, when small amounts of pyruvate were added to the reaction mixture, acid production rates and the glucose consumption rate were multiplied by a factor ranging from 2 to 3. These phenomena were paralleled by an increase in the NAD(+)/NADH ratio, thus corroborating the view that the efficient regeneration of NAD(+) could be triggered by the addition of either bicarbonate or pyruvate. To investigate the global metabolism of corynebacteria under oxygen deprivation conditions, we engineered several strains where the genes coding for key metabolic enzymes had been inactivated by gene disruption and replacement. A lactate dehydrogenase (LDH)-deficient mutant was not able to produce lactate, suggesting this enzyme has no other isozyme. Although a pyruvate carboxylase (pyc) mutant exhibited similar behavior to that of the wild type, phosphoenolpyruvate carboxylase (ppc) mutants were characterized by a dramatic decrease in succinate production, which was concomitant to decreased lactate production and glucose consumption rates. This set of observations corroborates the view that in coryneform bacteria under oxygen deprivation conditions the major anaplerotic reaction is driven by the ppc gene product rather than by the pyc gene product. Moreover, intracellular NADH concentrations in C. glutamicum were observed to correlate to oxygen-deprived metabolic flows. Copyright 2004 S. Karger AG, Basel

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Year:  2004        PMID: 15383716     DOI: 10.1159/000079827

Source DB:  PubMed          Journal:  J Mol Microbiol Biotechnol        ISSN: 1464-1801


  81 in total

1.  Toward homosuccinate fermentation: metabolic engineering of Corynebacterium glutamicum for anaerobic production of succinate from glucose and formate.

Authors:  Boris Litsanov; Melanie Brocker; Michael Bott
Journal:  Appl Environ Microbiol       Date:  2012-03-02       Impact factor: 4.792

2.  Succinic acid fermentation in a stationary-basket bioreactor with a packed bed of immobilized Actinobacillus succinogenes: 1. Influence of internal diffusion on substrate mass transfer and consumption rate.

Authors:  Anca-Irina Galaction; Lenuta Kloetzer; Marius Turnea; Colin Webb; Anestis Vlysidis; Dan Caşcaval
Journal:  J Ind Microbiol Biotechnol       Date:  2012-02-15       Impact factor: 3.346

3.  Translation efficiency of antiterminator proteins is a determinant for the difference in glucose repression of two β-glucoside phosphotransferase system gene clusters in Corynebacterium glutamicum R.

Authors:  Yuya Tanaka; Haruhiko Teramoto; Masayuki Inui; Hideaki Yukawa
Journal:  J Bacteriol       Date:  2010-11-12       Impact factor: 3.490

Review 4.  Engineering the glycolytic pathway: A potential approach for improvement of biocatalyst performance.

Authors:  Toru Jojima; Masayuki Inui
Journal:  Bioengineered       Date:  2015       Impact factor: 3.269

5.  Development of fatty acid-producing Corynebacterium glutamicum strains.

Authors:  Seiki Takeno; Manami Takasaki; Akinobu Urabayashi; Akinori Mimura; Tetsuhiro Muramatsu; Satoshi Mitsuhashi; Masato Ikeda
Journal:  Appl Environ Microbiol       Date:  2013-08-30       Impact factor: 4.792

6.  Anaerobic growth of Corynebacterium glutamicum via mixed-acid fermentation.

Authors:  Andrea Michel; Abigail Koch-Koerfges; Karin Krumbach; Melanie Brocker; Michael Bott
Journal:  Appl Environ Microbiol       Date:  2015-08-14       Impact factor: 4.792

Review 7.  Manipulating corynebacteria, from individual genes to chromosomes.

Authors:  Alain A Vertès; Masayuki Inui; Hideaki Yukawa
Journal:  Appl Environ Microbiol       Date:  2005-12       Impact factor: 4.792

8.  Corynebacterium glutamicum ArnR controls expression of nitrate reductase operon narKGHJI and nitric oxide (NO)-detoxifying enzyme gene hmp in an NO-responsive manner.

Authors:  Taku Nishimura; Haruhiko Teramoto; Masayuki Inui; Hideaki Yukawa
Journal:  J Bacteriol       Date:  2013-10-18       Impact factor: 3.490

9.  Group 2 sigma factor SigB of Corynebacterium glutamicum positively regulates glucose metabolism under conditions of oxygen deprivation.

Authors:  Shigeki Ehira; Tomokazu Shirai; Haruhiko Teramoto; Masayuki Inui; Hideaki Yukawa
Journal:  Appl Environ Microbiol       Date:  2008-06-20       Impact factor: 4.792

10.  Engineering of Corynebacterium glutamicum for high-yield L-valine production under oxygen deprivation conditions.

Authors:  Satoshi Hasegawa; Masako Suda; Kimio Uematsu; Yumi Natsuma; Kazumi Hiraga; Toru Jojima; Masayuki Inui; Hideaki Yukawa
Journal:  Appl Environ Microbiol       Date:  2012-12-14       Impact factor: 4.792

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