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Metabolic engineering of Escherichia coli for the production of butyric acid at high titer and productivity
BACKGROUND: Several anaerobic bacteria produce butyric acid, a commodity chemical with use in chemical, pharmaceutical, food and feed industries, using complex media with acetate as a co-product. Butyrate titer of various recombinant Escherichia coli did not exceed 10 g l(−1) in batch fermentations...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429758/ https://www.ncbi.nlm.nih.gov/pubmed/30949238 http://dx.doi.org/10.1186/s13068-019-1408-9 |
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author | Wang, Liang Chauliac, Diane Moritz, Brelan E. Zhang, Guimin Ingram, Lonnie O. Shanmugam, K. T. |
author_facet | Wang, Liang Chauliac, Diane Moritz, Brelan E. Zhang, Guimin Ingram, Lonnie O. Shanmugam, K. T. |
author_sort | Wang, Liang |
collection | PubMed |
description | BACKGROUND: Several anaerobic bacteria produce butyric acid, a commodity chemical with use in chemical, pharmaceutical, food and feed industries, using complex media with acetate as a co-product. Butyrate titer of various recombinant Escherichia coli did not exceed 10 g l(−1) in batch fermentations in any of the media tested. RESULTS: A recombinant E. coli (strain LW393) that produced butyrate as the major fermentation product was constructed with genes from E. coli, Clostridium acetobutylicum and Treponema denticola. Strain LW393 produced 323 ± 6 mM (28.4 ± 0.4 g l(−1)) butyric acid in batch fermentations in mineral salt medium with glucose as C source at a yield of 0.37 ± 0.01 g (g glucose consumed)(−1). Butyrate accounted for 90% of the total products produced by the culture. Supplementing this medium with yeast extract further increased butyric acid titer to 375 ± 4 mM. Average volumetric productivity of butyrate with xylose as C source was 0.89 ± 0.07 g l(−1) h(−1). CONCLUSIONS: The butyrate titer reported in this study is about 2.5–3-times higher than the values reported for other recombinant E. coli and this is achieved in mineral salt medium with an expectation of lower purification and production cost of butyrate. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-019-1408-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6429758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64297582019-04-04 Metabolic engineering of Escherichia coli for the production of butyric acid at high titer and productivity Wang, Liang Chauliac, Diane Moritz, Brelan E. Zhang, Guimin Ingram, Lonnie O. Shanmugam, K. T. Biotechnol Biofuels Research BACKGROUND: Several anaerobic bacteria produce butyric acid, a commodity chemical with use in chemical, pharmaceutical, food and feed industries, using complex media with acetate as a co-product. Butyrate titer of various recombinant Escherichia coli did not exceed 10 g l(−1) in batch fermentations in any of the media tested. RESULTS: A recombinant E. coli (strain LW393) that produced butyrate as the major fermentation product was constructed with genes from E. coli, Clostridium acetobutylicum and Treponema denticola. Strain LW393 produced 323 ± 6 mM (28.4 ± 0.4 g l(−1)) butyric acid in batch fermentations in mineral salt medium with glucose as C source at a yield of 0.37 ± 0.01 g (g glucose consumed)(−1). Butyrate accounted for 90% of the total products produced by the culture. Supplementing this medium with yeast extract further increased butyric acid titer to 375 ± 4 mM. Average volumetric productivity of butyrate with xylose as C source was 0.89 ± 0.07 g l(−1) h(−1). CONCLUSIONS: The butyrate titer reported in this study is about 2.5–3-times higher than the values reported for other recombinant E. coli and this is achieved in mineral salt medium with an expectation of lower purification and production cost of butyrate. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-019-1408-9) contains supplementary material, which is available to authorized users. BioMed Central 2019-03-22 /pmc/articles/PMC6429758/ /pubmed/30949238 http://dx.doi.org/10.1186/s13068-019-1408-9 Text en © The Author(s) 2019 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 Wang, Liang Chauliac, Diane Moritz, Brelan E. Zhang, Guimin Ingram, Lonnie O. Shanmugam, K. T. Metabolic engineering of Escherichia coli for the production of butyric acid at high titer and productivity |
title | Metabolic engineering of Escherichia coli for the production of butyric acid at high titer and productivity |
title_full | Metabolic engineering of Escherichia coli for the production of butyric acid at high titer and productivity |
title_fullStr | Metabolic engineering of Escherichia coli for the production of butyric acid at high titer and productivity |
title_full_unstemmed | Metabolic engineering of Escherichia coli for the production of butyric acid at high titer and productivity |
title_short | Metabolic engineering of Escherichia coli for the production of butyric acid at high titer and productivity |
title_sort | metabolic engineering of escherichia coli for the production of butyric acid at high titer and productivity |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429758/ https://www.ncbi.nlm.nih.gov/pubmed/30949238 http://dx.doi.org/10.1186/s13068-019-1408-9 |
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