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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...

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Autores principales: Radoš, Dušica, Carvalho, Ana Lúcia, Wieschalka, Stefan, Neves, Ana Rute, Blombach, Bastian, Eikmanns, Bernhard J., Santos, Helena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
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.
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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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