Literature DB >> 12450803

Genealogy profiling through strain improvement by using metabolic network analysis: metabolic flux genealogy of several generations of lysine-producing corynebacteria.

Christoph Wittmann1, Elmar Heinzle.   

Abstract

A comprehensive approach of metabolite balancing, (13)C tracer studies, gas chromatography-mass spectrometry, matrix-assisted laser desorption ionization-time of flight mass spectrometry, and isotopomer modeling was applied for comparative metabolic network analysis of a genealogy of five successive generations of lysine-producing Corynebacterium glutamicum. The five strains examined (C. glutamicum ATCC 13032, 13287, 21253, 21526, and 21543) were previously obtained by random mutagenesis and selection. Throughout the genealogy, the lysine yield in batch cultures increased markedly from 1.2 to 24.9% relative to the glucose uptake flux. Strain optimization was accompanied by significant changes in intracellular flux distributions. The relative pentose phosphate pathway (PPP) flux successively increased, clearly corresponding to the product yield. Moreover, the anaplerotic net flux increased almost twofold as a consequence of concerted regulation of C(3) carboxylation and C(4) decarboxylation fluxes to cover the increased demand for lysine formation; thus, the overall increase was a consequence of concerted regulation of C(3) carboxylation and C(4) decarboxylation fluxes. The relative flux through isocitrate dehydrogenase dropped from 82.7% in the wild type to 59.9% in the lysine-producing mutants. In contrast to the NADPH demand, which increased from 109 to 172% due to the increasing lysine yield, the overall NADPH supply remained constant between 185 and 196%, resulting in a decrease in the apparent NADPH excess through strain optimization. Extrapolated to industrial lysine producers, the NADPH supply might become a limiting factor. The relative contributions of PPP and the tricarboxylic acid cycle to NADPH generation changed markedly, indicating that C. glutamicum is able to maintain a constant supply of NADPH under completely different flux conditions. Statistical analysis by a Monte Carlo approach revealed high precision for the estimated fluxes, underlining the fact that the observed differences were clearly strain specific.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12450803      PMCID: PMC134428          DOI: 10.1128/AEM.68.12.5843-5859.2002

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  24 in total

1.  Mass spectrometry for metabolic flux analysis.

Authors: 
Journal:  Biotechnol Bioeng       Date:  1999-03       Impact factor: 4.530

Review 2.  Metabolic flux analysis using mass spectrometry.

Authors:  C Wittmann
Journal:  Adv Biochem Eng Biotechnol       Date:  2002       Impact factor: 2.635

3.  Correcting mass isotopomer distributions for naturally occurring isotopes.

Authors:  Wouter A van Winden; Christoph Wittmann; Elmar Heinzle; Joseph J Heijnen
Journal:  Biotechnol Bioeng       Date:  2002-11-20       Impact factor: 4.530

4.  Bidirectional reaction steps in metabolic networks: II. Flux estimation and statistical analysis.

Authors:  W Wiechert; C Siefke; A A de Graaf; A Marx
Journal:  Biotechnol Bioeng       Date:  1997-07-05       Impact factor: 4.530

5.  NADH dehydrogenase of Corynebacterium glutamicum. Purification of an NADH dehydrogenase II homolog able to oxidize NADPH.

Authors:  K Matsushita; A Otofuji; M Iwahashi; H Toyama; O Adachi
Journal:  FEMS Microbiol Lett       Date:  2001-11-13       Impact factor: 2.742

6.  Kinetic properties of the glucose-6-phosphate and 6-phosphogluconate dehydrogenases from Corynebacterium glutamicum and their application for predicting pentose phosphate pathway flux in vivo.

Authors:  B Moritz; K Striegel; A A De Graaf; H Sahm
Journal:  Eur J Biochem       Date:  2000-06

7.  Modeling and experimental design for metabolic flux analysis of lysine-producing Corynebacteria by mass spectrometry.

Authors:  C Wittmann; E Heinzle
Journal:  Metab Eng       Date:  2001-04       Impact factor: 9.783

8.  Determination of the fluxes in the central metabolism of Corynebacterium glutamicum by nuclear magnetic resonance spectroscopy combined with metabolite balancing.

Authors:  A Marx; A A de Graaf; W Wiechert; L Eggeling; H Sahm
Journal:  Biotechnol Bioeng       Date:  1996-01-20       Impact factor: 4.530

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

Authors:  J J Vallino; G Stephanopoulos
Journal:  Biotechnol Bioeng       Date:  1993-03-15       Impact factor: 4.530

10.  Cloning, sequence analysis, expression, and inactivation of the Corynebacterium glutamicum icd gene encoding isocitrate dehydrogenase and biochemical characterization of the enzyme.

Authors:  B J Eikmanns; D Rittmann; H Sahm
Journal:  J Bacteriol       Date:  1995-02       Impact factor: 3.490

View more
  38 in total

1.  Experimental identification and quantification of glucose metabolism in seven bacterial species.

Authors:  Tobias Fuhrer; Eliane Fischer; Uwe Sauer
Journal:  J Bacteriol       Date:  2005-03       Impact factor: 3.490

Review 2.  Microbial metabolomics: replacing trial-and-error by the unbiased selection and ranking of targets.

Authors:  Mariët J van der Werf; Renger H Jellema; Thomas Hankemeier
Journal:  J Ind Microbiol Biotechnol       Date:  2005-05-14       Impact factor: 3.346

Review 3.  Fermented foods: patented approaches and formulations for nutritional supplementation and health promotion.

Authors:  Erica C Borresen; Angela J Henderson; Ajay Kumar; Tiffany L Weir; Elizabeth P Ryan
Journal:  Recent Pat Food Nutr Agric       Date:  2012-08

4.  Amplified expression of fructose 1,6-bisphosphatase in Corynebacterium glutamicum increases in vivo flux through the pentose phosphate pathway and lysine production on different carbon sources.

Authors:  Judith Becker; Corinna Klopprogge; Oskar Zelder; Elmar Heinzle; Christoph Wittmann
Journal:  Appl Environ Microbiol       Date:  2005-12       Impact factor: 4.792

5.  Kinetic isotope effects significantly influence intracellular metabolite (13) C labeling patterns and flux determination.

Authors:  Thomas M Wasylenko; Gregory Stephanopoulos
Journal:  Biotechnol J       Date:  2013-08-05       Impact factor: 4.677

6.  Core fluxome and metafluxome of lactic acid bacteria under simulated cocoa pulp fermentation conditions.

Authors:  Philipp Adler; Christoph Josef Bolten; Katrin Dohnt; Carl Erik Hansen; Christoph Wittmann
Journal:  Appl Environ Microbiol       Date:  2013-07-12       Impact factor: 4.792

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

Authors:  Christoph Wittmann; Patrick Kiefer; Oskar Zelder
Journal:  Appl Environ Microbiol       Date:  2004-12       Impact factor: 4.792

8.  Implication of gluconate kinase activity in L-ornithine biosynthesis in Corynebacterium glutamicum.

Authors:  Gui-Hye Hwang; Jae-Yong Cho
Journal:  J Ind Microbiol Biotechnol       Date:  2012-09-18       Impact factor: 3.346

9.  Metabolic engineering of the tricarboxylic acid cycle for improved lysine production by Corynebacterium glutamicum.

Authors:  Judith Becker; Corinna Klopprogge; Hartwig Schröder; Christoph Wittmann
Journal:  Appl Environ Microbiol       Date:  2009-10-09       Impact factor: 4.792

10.  In-depth profiling of lysine-producing Corynebacterium glutamicum by combined analysis of the transcriptome, metabolome, and fluxome.

Authors:  Jens Olaf Krömer; Oliver Sorgenfrei; Kai Klopprogge; Elmar Heinzle; Christoph Wittmann
Journal:  J Bacteriol       Date:  2004-03       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.