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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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. |
format | Online Article Text |
id | pubmed-7181634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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