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Systematic engineering of the central metabolism in Escherichia coli for effective production of n-butanol
BACKGROUND: Microbes have been extensively explored for production of environment-friendly fuels and chemicals. The microbial fermentation pathways leading to these commodities usually involve many redox reactions. This makes the fermentative production of highly reduced products challenging, becaus...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799531/ https://www.ncbi.nlm.nih.gov/pubmed/26997975 http://dx.doi.org/10.1186/s13068-016-0467-4 |
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author | Saini, Mukesh Li, Si-Yu Wang, Ze Win Chiang, Chung-Jen Chao, Yun-Peng |
author_facet | Saini, Mukesh Li, Si-Yu Wang, Ze Win Chiang, Chung-Jen Chao, Yun-Peng |
author_sort | Saini, Mukesh |
collection | PubMed |
description | BACKGROUND: Microbes have been extensively explored for production of environment-friendly fuels and chemicals. The microbial fermentation pathways leading to these commodities usually involve many redox reactions. This makes the fermentative production of highly reduced products challenging, because there is a limited NADH output from glucose catabolism. Microbial production of n-butanol apparently represents one typical example. RESULTS: In this study, we addressed the issue by adjustment of the intracellular redox state in Escherichia coli. This was initiated with strain BuT-8 which carries the clostridial CoA-dependent synthetic pathway. Three metabolite nodes in the central metabolism of the strain were targeted for engineering. First, the pyruvate node was manipulated by enhancement of pyruvate decarboxylation in the oxidative pathway. Subsequently, the pentose phosphate (PP) pathway was amplified at the glucose-6-phosphate (G6P) node. The pathway for G6P isomerization was further blocked to force the glycolytic flux through the PP pathway. It resulted in a growth defect, and the cell growth was later recovered by limiting the tricarboxylic acid cycle at the acetyl-CoA node. Finally, the resulting strain exhibited a high NADH level and enabled production of 6.1 g/L n-butanol with a yield of 0.31 g/g-glucose and a productivity of 0.21 g/L/h. CONCLUSIONS: The production efficiency of fermentative products in microbes strongly depends on the intracellular redox state. This work illustrates the flexibility of pyruvate, G6P, and acetyl-CoA nodes at the junction of the central metabolism for engineering. In principle, high production of reduced products of interest can be achieved by individual or coordinated modulation of these metabolite nodes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-016-0467-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4799531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47995312016-03-20 Systematic engineering of the central metabolism in Escherichia coli for effective production of n-butanol Saini, Mukesh Li, Si-Yu Wang, Ze Win Chiang, Chung-Jen Chao, Yun-Peng Biotechnol Biofuels Research BACKGROUND: Microbes have been extensively explored for production of environment-friendly fuels and chemicals. The microbial fermentation pathways leading to these commodities usually involve many redox reactions. This makes the fermentative production of highly reduced products challenging, because there is a limited NADH output from glucose catabolism. Microbial production of n-butanol apparently represents one typical example. RESULTS: In this study, we addressed the issue by adjustment of the intracellular redox state in Escherichia coli. This was initiated with strain BuT-8 which carries the clostridial CoA-dependent synthetic pathway. Three metabolite nodes in the central metabolism of the strain were targeted for engineering. First, the pyruvate node was manipulated by enhancement of pyruvate decarboxylation in the oxidative pathway. Subsequently, the pentose phosphate (PP) pathway was amplified at the glucose-6-phosphate (G6P) node. The pathway for G6P isomerization was further blocked to force the glycolytic flux through the PP pathway. It resulted in a growth defect, and the cell growth was later recovered by limiting the tricarboxylic acid cycle at the acetyl-CoA node. Finally, the resulting strain exhibited a high NADH level and enabled production of 6.1 g/L n-butanol with a yield of 0.31 g/g-glucose and a productivity of 0.21 g/L/h. CONCLUSIONS: The production efficiency of fermentative products in microbes strongly depends on the intracellular redox state. This work illustrates the flexibility of pyruvate, G6P, and acetyl-CoA nodes at the junction of the central metabolism for engineering. In principle, high production of reduced products of interest can be achieved by individual or coordinated modulation of these metabolite nodes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-016-0467-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-03-18 /pmc/articles/PMC4799531/ /pubmed/26997975 http://dx.doi.org/10.1186/s13068-016-0467-4 Text en © Saini et al. 2016 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 Saini, Mukesh Li, Si-Yu Wang, Ze Win Chiang, Chung-Jen Chao, Yun-Peng Systematic engineering of the central metabolism in Escherichia coli for effective production of n-butanol |
title | Systematic engineering of the central metabolism in Escherichia coli for effective production of n-butanol |
title_full | Systematic engineering of the central metabolism in Escherichia coli for effective production of n-butanol |
title_fullStr | Systematic engineering of the central metabolism in Escherichia coli for effective production of n-butanol |
title_full_unstemmed | Systematic engineering of the central metabolism in Escherichia coli for effective production of n-butanol |
title_short | Systematic engineering of the central metabolism in Escherichia coli for effective production of n-butanol |
title_sort | systematic engineering of the central metabolism in escherichia coli for effective production of n-butanol |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799531/ https://www.ncbi.nlm.nih.gov/pubmed/26997975 http://dx.doi.org/10.1186/s13068-016-0467-4 |
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