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One-pot biocatalytic route from cycloalkanes to α,ω‐dicarboxylic acids by designed Escherichia coli consortia
Aliphatic α,ω‐dicarboxylic acids (DCAs) are a class of useful chemicals that are currently produced by energy-intensive, multistage chemical oxidations that are hazardous to the environment. Therefore, the development of environmentally friendly, safe, neutral routes to DCAs is important. We report...
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/PMC7542165/ https://www.ncbi.nlm.nih.gov/pubmed/33028823 http://dx.doi.org/10.1038/s41467-020-18833-7 |
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author | Wang, Fei Zhao, Jing Li, Qian Yang, Jun Li, Renjie Min, Jian Yu, Xiaojuan Zheng, Gao-Wei Yu, Hui-Lei Zhai, Chao Acevedo-Rocha, Carlos G. Ma, Lixin Li, Aitao |
author_facet | Wang, Fei Zhao, Jing Li, Qian Yang, Jun Li, Renjie Min, Jian Yu, Xiaojuan Zheng, Gao-Wei Yu, Hui-Lei Zhai, Chao Acevedo-Rocha, Carlos G. Ma, Lixin Li, Aitao |
author_sort | Wang, Fei |
collection | PubMed |
description | Aliphatic α,ω‐dicarboxylic acids (DCAs) are a class of useful chemicals that are currently produced by energy-intensive, multistage chemical oxidations that are hazardous to the environment. Therefore, the development of environmentally friendly, safe, neutral routes to DCAs is important. We report an in vivo artificially designed biocatalytic cascade process for biotransformation of cycloalkanes to DCAs. To reduce protein expression burden and redox constraints caused by multi-enzyme expression in a single microbe, the biocatalytic pathway is divided into three basic Escherichia coli cell modules. The modules possess either redox-neutral or redox-regeneration systems and are combined to form E. coli consortia for use in biotransformations. The designed consortia of E. coli containing the modules efficiently convert cycloalkanes or cycloalkanols to DCAs without addition of exogenous coenzymes. Thus, this developed biocatalytic process provides a promising alternative to the current industrial process for manufacturing DCAs. |
format | Online Article Text |
id | pubmed-7542165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75421652020-10-19 One-pot biocatalytic route from cycloalkanes to α,ω‐dicarboxylic acids by designed Escherichia coli consortia Wang, Fei Zhao, Jing Li, Qian Yang, Jun Li, Renjie Min, Jian Yu, Xiaojuan Zheng, Gao-Wei Yu, Hui-Lei Zhai, Chao Acevedo-Rocha, Carlos G. Ma, Lixin Li, Aitao Nat Commun Article Aliphatic α,ω‐dicarboxylic acids (DCAs) are a class of useful chemicals that are currently produced by energy-intensive, multistage chemical oxidations that are hazardous to the environment. Therefore, the development of environmentally friendly, safe, neutral routes to DCAs is important. We report an in vivo artificially designed biocatalytic cascade process for biotransformation of cycloalkanes to DCAs. To reduce protein expression burden and redox constraints caused by multi-enzyme expression in a single microbe, the biocatalytic pathway is divided into three basic Escherichia coli cell modules. The modules possess either redox-neutral or redox-regeneration systems and are combined to form E. coli consortia for use in biotransformations. The designed consortia of E. coli containing the modules efficiently convert cycloalkanes or cycloalkanols to DCAs without addition of exogenous coenzymes. Thus, this developed biocatalytic process provides a promising alternative to the current industrial process for manufacturing DCAs. Nature Publishing Group UK 2020-10-07 /pmc/articles/PMC7542165/ /pubmed/33028823 http://dx.doi.org/10.1038/s41467-020-18833-7 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 Wang, Fei Zhao, Jing Li, Qian Yang, Jun Li, Renjie Min, Jian Yu, Xiaojuan Zheng, Gao-Wei Yu, Hui-Lei Zhai, Chao Acevedo-Rocha, Carlos G. Ma, Lixin Li, Aitao One-pot biocatalytic route from cycloalkanes to α,ω‐dicarboxylic acids by designed Escherichia coli consortia |
title | One-pot biocatalytic route from cycloalkanes to α,ω‐dicarboxylic acids by designed Escherichia coli consortia |
title_full | One-pot biocatalytic route from cycloalkanes to α,ω‐dicarboxylic acids by designed Escherichia coli consortia |
title_fullStr | One-pot biocatalytic route from cycloalkanes to α,ω‐dicarboxylic acids by designed Escherichia coli consortia |
title_full_unstemmed | One-pot biocatalytic route from cycloalkanes to α,ω‐dicarboxylic acids by designed Escherichia coli consortia |
title_short | One-pot biocatalytic route from cycloalkanes to α,ω‐dicarboxylic acids by designed Escherichia coli consortia |
title_sort | one-pot biocatalytic route from cycloalkanes to α,ω‐dicarboxylic acids by designed escherichia coli consortia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542165/ https://www.ncbi.nlm.nih.gov/pubmed/33028823 http://dx.doi.org/10.1038/s41467-020-18833-7 |
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