Literature DB >> 30392965

Corynebacterium glutamicum CgynfM encodes a dicarboxylate transporter applicable to succinate production.

Keita Fukui1, Kei Nanatani2, Mayumi Nakayama2, Yoshihiko Hara3, Mitsunori Tokura3, Keietsu Abe4.   

Abstract

After deleting the gene encoding succinate dehydrogenase, Corynebacterium glutamicum can produce succinate and a considerable amount of acetate and pyruvate as by-products from glucose metabolism, under aerobic conditions. Recently, we identified ynfM in Pantoea ananatis (PaynfM) as a gene encoding a dicarboxylate transporter and found a homologous gene (CgynfM) in C. glutamicum. In this study, we examined dicarboxylate production using C. glutamicum strains expressing CgynfM. When C. glutamicum expressing the CgynfM gene was cultured under aerobic conditions, the sugar-consumption rate increased significantly, succinate accumulation increased from 66 mM to 110 mM, and pyruvate and acetate co-production decreased significantly. Pyruvate decreased from 120 mM to 6.2 mM, and acetate decreased to undetectable level. CgYnfM restored succinate production under anaerobic conditions in C. glutamicum strain AJ110655ΔsucE1, in which the gene encoding the major succinate exporter (sucE1) was deleted. CgynfM expression also increased α-ketoglutarate production from 5.1 mM to 24 mM under anaerobic conditions. Collectively, these results suggest that YnfM from C. glutamicum functions as a dicarboxylate transporter that is applicable to the succinate production.
Copyright © 2018 The Society for Biotechnology, Japan. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Aerobic conditions; Anaerobic conditions; Corynebacterium glutamicum; Dicarboxylate transporter; Succinate production; α-Ketoglutarate production

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Year:  2018        PMID: 30392965     DOI: 10.1016/j.jbiosc.2018.10.004

Source DB:  PubMed          Journal:  J Biosci Bioeng        ISSN: 1347-4421            Impact factor:   2.894


  4 in total

1.  Glutaric acid production by systems metabolic engineering of an l-lysine-overproducing Corynebacterium glutamicum.

Authors:  Taehee Han; Gi Bae Kim; Sang Yup Lee
Journal:  Proc Natl Acad Sci U S A       Date:  2020-11-16       Impact factor: 11.205

2.  Construction and application of a CRISPR/Cas9-assisted genomic editing system for Corynebacterium glutamicum.

Authors:  Chengzhen Yao; Xiaoqing Hu; Xiaoyuan Wang
Journal:  AMB Express       Date:  2021-05-19       Impact factor: 3.298

3.  Engineering energetically efficient transport of dicarboxylic acids in yeast Saccharomyces cerevisiae.

Authors:  Behrooz Darbani; Vratislav Stovicek; Steven Axel van der Hoek; Irina Borodina
Journal:  Proc Natl Acad Sci U S A       Date:  2019-08-29       Impact factor: 11.205

4.  Fermentative Production of l-2-Hydroxyglutarate by Engineered Corynebacterium glutamicum via Pathway Extension of l-Lysine Biosynthesis.

Authors:  Carina Prell; Arthur Burgardt; Florian Meyer; Volker F Wendisch
Journal:  Front Bioeng Biotechnol       Date:  2021-01-27
  4 in total

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