Literature DB >> 20118267

Alternative route for glyoxylate consumption during growth on two-carbon compounds by Methylobacterium extorquens AM1.

Yoko Okubo1, Song Yang, Ludmila Chistoserdova, Mary E Lidstrom.   

Abstract

Methylobacterium extorquens AM1 is a facultative methylotroph capable of growth on both single-carbon and multicarbon compounds. Mutants defective in a pathway involved in converting acetyl-coenzyme A (CoA) to glyoxylate (the ethylmalonyl-CoA pathway) are unable to grow on both C(1) and C(2) compounds, showing that both modes of growth have this pathway in common. However, growth on C(2) compounds via the ethylmalonyl-CoA pathway should require glyoxylate consumption via malate synthase, but a mutant lacking malyl-CoA/beta-methylmalyl-CoA lyase activity (MclA1) that is assumed to be responsible for malate synthase activity still grows on C(2) compounds. Since glyoxylate is toxic to this bacterium, it seemed likely that a system is in place to keep it from accumulating. In this study, we have addressed this question and have shown by microarray analysis, mutant analysis, metabolite measurements, and (13)C-labeling experiments that M. extorquens AM1 contains an additional malyl-CoA/beta-methylmalyl-CoA lyase (MclA2) that appears to take part in glyoxylate metabolism during growth on C(2) compounds. In addition, an alternative pathway appears to be responsible for consuming part of the glyoxylate, converting it to glycine, methylene-H(4)F, and serine. Mutants lacking either pathway have a partial defect for growth on ethylamine, while mutants lacking both pathways are unable to grow appreciably on ethylamine. Our results suggest that the malate synthase reaction is a bottleneck for growth on C(2) compounds by this bacterium, which is partially alleviated by this alternative route for glyoxylate consumption. This strategy of multiple enzymes/pathways for the consumption of a toxic intermediate reflects the metabolic versatility of this facultative methylotroph and is a model for other metabolic networks involving high flux through toxic intermediates.

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Year:  2010        PMID: 20118267      PMCID: PMC2838054          DOI: 10.1128/JB.01166-09

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  49 in total

1.  Mass spectrometry for metabolic flux analysis.

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

2.  Synthesis and hydrolysis of malyl-coenzyme A by Pseudomonas AM1: an apparent malate synthase activity.

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Journal:  J Gen Microbiol       Date:  1976-07

3.  Study of an alternate glyoxylate cycle for acetate assimilation by Rhodobacter sphaeroides.

Authors:  Birgit E Alber; Regina Spanheimer; Christa Ebenau-Jehle; Georg Fuchs
Journal:  Mol Microbiol       Date:  2006-07       Impact factor: 3.501

4.  L-malyl-coenzyme A/beta-methylmalyl-coenzyme A lyase is involved in acetate assimilation of the isocitrate lyase-negative bacterium Rhodobacter capsulatus.

Authors:  Michael Meister; Stephan Saum; Birgit E Alber; Georg Fuchs
Journal:  J Bacteriol       Date:  2005-02       Impact factor: 3.490

5.  Molecular characterization of a chromosomal region involved in the oxidation of acetyl-CoA to glyoxylate in the isocitrate-lyase-negative methylotroph Methylobacterium extorquens AM1.

Authors:  Ludmila V Chistoserdova; Mary E Lidstrom
Journal:  Microbiology (Reading)       Date:  1996-06       Impact factor: 2.777

6.  Purification and properties of malyl-coenzyme A lyase from Pseudomonas AM1.

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Journal:  Biochem J       Date:  1974-05       Impact factor: 3.857

7.  Liquid chromatography-tandem quadrupole mass spectrometry and comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry measurement of targeted metabolites of Methylobacterium extorquens AM1 grown on two different carbon sources.

Authors:  Song Yang; Martin Sadilek; Robert E Synovec; Mary E Lidstrom
Journal:  J Chromatogr A       Date:  2009-02-21       Impact factor: 4.759

8.  Genetic organization of the mau gene cluster in Methylobacterium extorquens AM1: complete nucleotide sequence and generation and characteristics of mau mutants.

Authors:  A Y Chistoserdov; L V Chistoserdova; W S McIntire; M E Lidstrom
Journal:  J Bacteriol       Date:  1994-07       Impact factor: 3.490

9.  The biosynthesis of serine and glycine in Pseudomonas AM1 with special reference to growth on carbon sources other than C1 compounds.

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Journal:  Biochem J       Date:  1971-03       Impact factor: 3.857

10.  Methanol dissimilation in Xanthobacter H4-14: activities, induction and comparison to Pseudomonas AM1 and Paracoccus denitrificans.

Authors:  C A Weaver; M E Lidstrom
Journal:  J Gen Microbiol       Date:  1985-09
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  17 in total

1.  CcrR, a TetR family transcriptional regulator, activates the transcription of a gene of the Ethylmalonyl coenzyme A pathway in Methylobacterium extorquens AM1.

Authors:  Bo Hu; Mary Lidstrom
Journal:  J Bacteriol       Date:  2012-03-23       Impact factor: 3.490

2.  Coassimilation of organic substrates via the autotrophic 3-hydroxypropionate bi-cycle in Chloroflexus aurantiacus.

Authors:  Jan Zarzycki; Georg Fuchs
Journal:  Appl Environ Microbiol       Date:  2011-07-15       Impact factor: 4.792

3.  The ethylmalonyl-CoA pathway is used in place of the glyoxylate cycle by Methylobacterium extorquens AM1 during growth on acetate.

Authors:  Kathrin Schneider; Rémi Peyraud; Patrick Kiefer; Philipp Christen; Nathanaël Delmotte; Stéphane Massou; Jean-Charles Portais; Julia A Vorholt
Journal:  J Biol Chem       Date:  2011-11-21       Impact factor: 5.157

Review 4.  Recent advances in mapping environmental microbial metabolisms through 13C isotopic fingerprints.

Authors:  Joseph Kuo-Hsiang Tang; Le You; Robert E Blankenship; Yinjie J Tang
Journal:  J R Soc Interface       Date:  2012-08-15       Impact factor: 4.118

5.  Ethylmalonyl coenzyme A mutase operates as a metabolic control point in Methylobacterium extorquens AM1.

Authors:  Nathan M Good; N Cecilia Martinez-Gomez; David A C Beck; Mary E Lidstrom
Journal:  J Bacteriol       Date:  2014-12-01       Impact factor: 3.490

6.  Streamlined pentafluorophenylpropyl column liquid chromatography-tandem quadrupole mass spectrometry and global (13)C-labeled internal standards improve performance for quantitative metabolomics in bacteria.

Authors:  Song Yang; Martin Sadilek; Mary E Lidstrom
Journal:  J Chromatogr A       Date:  2010-09-29       Impact factor: 4.759

7.  Oxalyl-coenzyme A reduction to glyoxylate is the preferred route of oxalate assimilation in Methylobacterium extorquens AM1.

Authors:  Kathrin Schneider; Elizabeth Skovran; Julia A Vorholt
Journal:  J Bacteriol       Date:  2012-04-06       Impact factor: 3.490

8.  Methanol assimilation in Methylobacterium extorquens AM1: demonstration of all enzymes and their regulation.

Authors:  Hana Smejkalová; Tobias J Erb; Georg Fuchs
Journal:  PLoS One       Date:  2010-10-01       Impact factor: 3.240

9.  Profiling of cytosolic and peroxisomal acetyl-CoA metabolism in Saccharomyces cerevisiae.

Authors:  Yun Chen; Verena Siewers; Jens Nielsen
Journal:  PLoS One       Date:  2012-08-02       Impact factor: 3.240

10.  Genome-scale reconstruction and system level investigation of the metabolic network of Methylobacterium extorquens AM1.

Authors:  Rémi Peyraud; Kathrin Schneider; Patrick Kiefer; Stéphane Massou; Julia A Vorholt; Jean-Charles Portais
Journal:  BMC Syst Biol       Date:  2011-11-10
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