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Engineering Corynebacterium glutamicum for the production of 2,3-butanediol
BACKGROUND: 2,3-Butanediol is an important bulk chemical with a wide range of applications. In bacteria, this metabolite is synthesised from pyruvate via a three-step pathway involving α-acetolactate synthase, α-acetolactate decarboxylase and 2,3-butanediol dehydrogenase. Thus far, the best producer...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625470/ https://www.ncbi.nlm.nih.gov/pubmed/26511723 http://dx.doi.org/10.1186/s12934-015-0362-x |
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author | Radoš, Dušica Carvalho, Ana Lúcia Wieschalka, Stefan Neves, Ana Rute Blombach, Bastian Eikmanns, Bernhard J. Santos, Helena |
author_facet | Radoš, Dušica Carvalho, Ana Lúcia Wieschalka, Stefan Neves, Ana Rute Blombach, Bastian Eikmanns, Bernhard J. Santos, Helena |
author_sort | Radoš, Dušica |
collection | PubMed |
description | BACKGROUND: 2,3-Butanediol is an important bulk chemical with a wide range of applications. In bacteria, this metabolite is synthesised from pyruvate via a three-step pathway involving α-acetolactate synthase, α-acetolactate decarboxylase and 2,3-butanediol dehydrogenase. Thus far, the best producers of 2,3-butanediol are pathogenic strains, hence, the development of more suitable organisms for industrial scale fermentation is needed. Herein, 2,3-butanediol production was engineered in the Generally Regarded As Safe (GRAS) organism Corynebacterium glutamicum. A two-stage fermentation process was implemented: first, cells were grown aerobically on acetate; in the subsequent production stage cells were used to convert glucose into 2,3-butanediol under non-growing and oxygen-limiting conditions. RESULTS: A gene cluster, encoding the 2,3-butanediol biosynthetic pathway of Lactococcus lactis, was assembled and expressed in background strains, C. glutamicum ΔldhA, C. glutamicum ΔaceEΔpqoΔldhA and C. glutamicum ΔaceEΔpqoΔldhAΔmdh, tailored to minimize pyruvate-consuming reactions, i.e., to prevent carbon loss in lactic, acetic and succinic acids. Producer strains were characterized in terms of activity of the relevant enzymes in the 2,3-butanediol forming pathway, growth, and production of 2,3-butanediol under oxygen-limited conditions. Productivity was maximized by manipulating the aeration rate in the production phase. The final strain, C. glutamicum ΔaceEΔpqoΔldhAΔmdh(pEKEx2-als,aldB,P(tuf)butA), under optimized conditions produced 2,3-butanediol with a 0.66 mol mol(−1) yield on glucose, an overall productivity of 0.2 g L(−1) h(−1) and a titer of 6.3 g L(−1). CONCLUSIONS: We have successfully developed C. glutamicum into an efficient cell factory for 2,3-butanediol production. The use of the engineered strains as a basis for production of acetoin, a widespread food flavour, is proposed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-015-0362-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4625470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46254702015-10-30 Engineering Corynebacterium glutamicum for the production of 2,3-butanediol Radoš, Dušica Carvalho, Ana Lúcia Wieschalka, Stefan Neves, Ana Rute Blombach, Bastian Eikmanns, Bernhard J. Santos, Helena Microb Cell Fact Research BACKGROUND: 2,3-Butanediol is an important bulk chemical with a wide range of applications. In bacteria, this metabolite is synthesised from pyruvate via a three-step pathway involving α-acetolactate synthase, α-acetolactate decarboxylase and 2,3-butanediol dehydrogenase. Thus far, the best producers of 2,3-butanediol are pathogenic strains, hence, the development of more suitable organisms for industrial scale fermentation is needed. Herein, 2,3-butanediol production was engineered in the Generally Regarded As Safe (GRAS) organism Corynebacterium glutamicum. A two-stage fermentation process was implemented: first, cells were grown aerobically on acetate; in the subsequent production stage cells were used to convert glucose into 2,3-butanediol under non-growing and oxygen-limiting conditions. RESULTS: A gene cluster, encoding the 2,3-butanediol biosynthetic pathway of Lactococcus lactis, was assembled and expressed in background strains, C. glutamicum ΔldhA, C. glutamicum ΔaceEΔpqoΔldhA and C. glutamicum ΔaceEΔpqoΔldhAΔmdh, tailored to minimize pyruvate-consuming reactions, i.e., to prevent carbon loss in lactic, acetic and succinic acids. Producer strains were characterized in terms of activity of the relevant enzymes in the 2,3-butanediol forming pathway, growth, and production of 2,3-butanediol under oxygen-limited conditions. Productivity was maximized by manipulating the aeration rate in the production phase. The final strain, C. glutamicum ΔaceEΔpqoΔldhAΔmdh(pEKEx2-als,aldB,P(tuf)butA), under optimized conditions produced 2,3-butanediol with a 0.66 mol mol(−1) yield on glucose, an overall productivity of 0.2 g L(−1) h(−1) and a titer of 6.3 g L(−1). CONCLUSIONS: We have successfully developed C. glutamicum into an efficient cell factory for 2,3-butanediol production. The use of the engineered strains as a basis for production of acetoin, a widespread food flavour, is proposed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-015-0362-x) contains supplementary material, which is available to authorized users. BioMed Central 2015-10-29 /pmc/articles/PMC4625470/ /pubmed/26511723 http://dx.doi.org/10.1186/s12934-015-0362-x Text en © Radoš et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Radoš, Dušica Carvalho, Ana Lúcia Wieschalka, Stefan Neves, Ana Rute Blombach, Bastian Eikmanns, Bernhard J. Santos, Helena Engineering Corynebacterium glutamicum for the production of 2,3-butanediol |
title | Engineering Corynebacterium glutamicum for the production of 2,3-butanediol |
title_full | Engineering Corynebacterium glutamicum for the production of 2,3-butanediol |
title_fullStr | Engineering Corynebacterium glutamicum for the production of 2,3-butanediol |
title_full_unstemmed | Engineering Corynebacterium glutamicum for the production of 2,3-butanediol |
title_short | Engineering Corynebacterium glutamicum for the production of 2,3-butanediol |
title_sort | engineering corynebacterium glutamicum for the production of 2,3-butanediol |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625470/ https://www.ncbi.nlm.nih.gov/pubmed/26511723 http://dx.doi.org/10.1186/s12934-015-0362-x |
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