Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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
_version_ 1783591506682052608
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
work_keys_str_mv AT wangfei onepotbiocatalyticroutefromcycloalkanestoaōdicarboxylicacidsbydesignedescherichiacoliconsortia
AT zhaojing onepotbiocatalyticroutefromcycloalkanestoaōdicarboxylicacidsbydesignedescherichiacoliconsortia
AT liqian onepotbiocatalyticroutefromcycloalkanestoaōdicarboxylicacidsbydesignedescherichiacoliconsortia
AT yangjun onepotbiocatalyticroutefromcycloalkanestoaōdicarboxylicacidsbydesignedescherichiacoliconsortia
AT lirenjie onepotbiocatalyticroutefromcycloalkanestoaōdicarboxylicacidsbydesignedescherichiacoliconsortia
AT minjian onepotbiocatalyticroutefromcycloalkanestoaōdicarboxylicacidsbydesignedescherichiacoliconsortia
AT yuxiaojuan onepotbiocatalyticroutefromcycloalkanestoaōdicarboxylicacidsbydesignedescherichiacoliconsortia
AT zhenggaowei onepotbiocatalyticroutefromcycloalkanestoaōdicarboxylicacidsbydesignedescherichiacoliconsortia
AT yuhuilei onepotbiocatalyticroutefromcycloalkanestoaōdicarboxylicacidsbydesignedescherichiacoliconsortia
AT zhaichao onepotbiocatalyticroutefromcycloalkanestoaōdicarboxylicacidsbydesignedescherichiacoliconsortia
AT acevedorochacarlosg onepotbiocatalyticroutefromcycloalkanestoaōdicarboxylicacidsbydesignedescherichiacoliconsortia
AT malixin onepotbiocatalyticroutefromcycloalkanestoaōdicarboxylicacidsbydesignedescherichiacoliconsortia
AT liaitao onepotbiocatalyticroutefromcycloalkanestoaōdicarboxylicacidsbydesignedescherichiacoliconsortia