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Enhanced succinic acid production by Mannheimia employing optimal malate dehydrogenase

Succinic acid (SA), a dicarboxylic acid of industrial importance, can be efficiently produced by metabolically engineered Mannheimia succiniciproducens. Malate dehydrogenase (MDH) is one of the key enzymes for SA production, but has not been well characterized. Here we report biochemical and structu...

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Autores principales: Ahn, Jung Ho, Seo, Hogyun, Park, Woojin, Seok, Jihye, Lee, Jong An, Kim, Won Jun, Kim, Gi Bae, Kim, Kyung-Jin, Lee, Sang Yup
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181634/
https://www.ncbi.nlm.nih.gov/pubmed/32327663
http://dx.doi.org/10.1038/s41467-020-15839-z
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author Ahn, Jung Ho
Seo, Hogyun
Park, Woojin
Seok, Jihye
Lee, Jong An
Kim, Won Jun
Kim, Gi Bae
Kim, Kyung-Jin
Lee, Sang Yup
author_facet Ahn, Jung Ho
Seo, Hogyun
Park, Woojin
Seok, Jihye
Lee, Jong An
Kim, Won Jun
Kim, Gi Bae
Kim, Kyung-Jin
Lee, Sang Yup
author_sort Ahn, Jung Ho
collection PubMed
description Succinic acid (SA), a dicarboxylic acid of industrial importance, can be efficiently produced by metabolically engineered Mannheimia succiniciproducens. Malate dehydrogenase (MDH) is one of the key enzymes for SA production, but has not been well characterized. Here we report biochemical and structural analyses of various MDHs and development of hyper-SA producing M. succiniciproducens by introducing the best MDH. Corynebacterium glutamicum MDH (CgMDH) shows the highest specific activity and least substrate inhibition, whereas M. succiniciproducens MDH (MsMDH) shows low specific activity at physiological pH and strong uncompetitive inhibition toward oxaloacetate (ki of 67.4 and 588.9 μM for MsMDH and CgMDH, respectively). Structural comparison of the two MDHs reveals a key residue influencing the specific activity and susceptibility to substrate inhibition. A high-inoculum fed-batch fermentation of the final strain expressing cgmdh produces 134.25 g L(−1) of SA with the maximum productivity of 21.3 g L(−1) h(−1), demonstrating the importance of enzyme optimization in strain development.
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spelling pubmed-71816342020-04-29 Enhanced succinic acid production by Mannheimia employing optimal malate dehydrogenase Ahn, Jung Ho Seo, Hogyun Park, Woojin Seok, Jihye Lee, Jong An Kim, Won Jun Kim, Gi Bae Kim, Kyung-Jin Lee, Sang Yup Nat Commun Article Succinic acid (SA), a dicarboxylic acid of industrial importance, can be efficiently produced by metabolically engineered Mannheimia succiniciproducens. Malate dehydrogenase (MDH) is one of the key enzymes for SA production, but has not been well characterized. Here we report biochemical and structural analyses of various MDHs and development of hyper-SA producing M. succiniciproducens by introducing the best MDH. Corynebacterium glutamicum MDH (CgMDH) shows the highest specific activity and least substrate inhibition, whereas M. succiniciproducens MDH (MsMDH) shows low specific activity at physiological pH and strong uncompetitive inhibition toward oxaloacetate (ki of 67.4 and 588.9 μM for MsMDH and CgMDH, respectively). Structural comparison of the two MDHs reveals a key residue influencing the specific activity and susceptibility to substrate inhibition. A high-inoculum fed-batch fermentation of the final strain expressing cgmdh produces 134.25 g L(−1) of SA with the maximum productivity of 21.3 g L(−1) h(−1), demonstrating the importance of enzyme optimization in strain development. Nature Publishing Group UK 2020-04-23 /pmc/articles/PMC7181634/ /pubmed/32327663 http://dx.doi.org/10.1038/s41467-020-15839-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ahn, Jung Ho
Seo, Hogyun
Park, Woojin
Seok, Jihye
Lee, Jong An
Kim, Won Jun
Kim, Gi Bae
Kim, Kyung-Jin
Lee, Sang Yup
Enhanced succinic acid production by Mannheimia employing optimal malate dehydrogenase
title Enhanced succinic acid production by Mannheimia employing optimal malate dehydrogenase
title_full Enhanced succinic acid production by Mannheimia employing optimal malate dehydrogenase
title_fullStr Enhanced succinic acid production by Mannheimia employing optimal malate dehydrogenase
title_full_unstemmed Enhanced succinic acid production by Mannheimia employing optimal malate dehydrogenase
title_short Enhanced succinic acid production by Mannheimia employing optimal malate dehydrogenase
title_sort enhanced succinic acid production by mannheimia employing optimal malate dehydrogenase
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181634/
https://www.ncbi.nlm.nih.gov/pubmed/32327663
http://dx.doi.org/10.1038/s41467-020-15839-z
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