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Chemo-enzymatic cascades to produce cycloalkenes from bio-based resources
Engineered enzyme cascades offer powerful tools to convert renewable resources into value-added products. Man-made catalysts give access to new-to-nature reactivities that may complement the enzyme’s repertoire. Their mutual incompatibility, however, challenges their integration into concurrent chem...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838201/ https://www.ncbi.nlm.nih.gov/pubmed/31699986 http://dx.doi.org/10.1038/s41467-019-13071-y |
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author | Wu, Shuke Zhou, Yi Gerngross, Daniel Jeschek, Markus Ward, Thomas R. |
author_facet | Wu, Shuke Zhou, Yi Gerngross, Daniel Jeschek, Markus Ward, Thomas R. |
author_sort | Wu, Shuke |
collection | PubMed |
description | Engineered enzyme cascades offer powerful tools to convert renewable resources into value-added products. Man-made catalysts give access to new-to-nature reactivities that may complement the enzyme’s repertoire. Their mutual incompatibility, however, challenges their integration into concurrent chemo-enzymatic cascades. Herein we show that compartmentalization of complex enzyme cascades within E. coli whole cells enables the simultaneous use of a metathesis catalyst, thus allowing the sustainable one-pot production of cycloalkenes from oleic acid. Cycloheptene is produced from oleic acid via a concurrent enzymatic oxidative decarboxylation and ring-closing metathesis. Cyclohexene and cyclopentene are produced from oleic acid via either a six- or eight-step enzyme cascade involving hydration, oxidation, hydrolysis and decarboxylation, followed by ring-closing metathesis. Integration of an upstream hydrolase enables the usage of olive oil as the substrate for the production of cycloalkenes. This work highlights the potential of integrating organometallic catalysis with whole-cell enzyme cascades of high complexity to enable sustainable chemistry. |
format | Online Article Text |
id | pubmed-6838201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68382012019-11-12 Chemo-enzymatic cascades to produce cycloalkenes from bio-based resources Wu, Shuke Zhou, Yi Gerngross, Daniel Jeschek, Markus Ward, Thomas R. Nat Commun Article Engineered enzyme cascades offer powerful tools to convert renewable resources into value-added products. Man-made catalysts give access to new-to-nature reactivities that may complement the enzyme’s repertoire. Their mutual incompatibility, however, challenges their integration into concurrent chemo-enzymatic cascades. Herein we show that compartmentalization of complex enzyme cascades within E. coli whole cells enables the simultaneous use of a metathesis catalyst, thus allowing the sustainable one-pot production of cycloalkenes from oleic acid. Cycloheptene is produced from oleic acid via a concurrent enzymatic oxidative decarboxylation and ring-closing metathesis. Cyclohexene and cyclopentene are produced from oleic acid via either a six- or eight-step enzyme cascade involving hydration, oxidation, hydrolysis and decarboxylation, followed by ring-closing metathesis. Integration of an upstream hydrolase enables the usage of olive oil as the substrate for the production of cycloalkenes. This work highlights the potential of integrating organometallic catalysis with whole-cell enzyme cascades of high complexity to enable sustainable chemistry. Nature Publishing Group UK 2019-11-07 /pmc/articles/PMC6838201/ /pubmed/31699986 http://dx.doi.org/10.1038/s41467-019-13071-y Text en © The Author(s) 2019 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 Wu, Shuke Zhou, Yi Gerngross, Daniel Jeschek, Markus Ward, Thomas R. Chemo-enzymatic cascades to produce cycloalkenes from bio-based resources |
title | Chemo-enzymatic cascades to produce cycloalkenes from bio-based resources |
title_full | Chemo-enzymatic cascades to produce cycloalkenes from bio-based resources |
title_fullStr | Chemo-enzymatic cascades to produce cycloalkenes from bio-based resources |
title_full_unstemmed | Chemo-enzymatic cascades to produce cycloalkenes from bio-based resources |
title_short | Chemo-enzymatic cascades to produce cycloalkenes from bio-based resources |
title_sort | chemo-enzymatic cascades to produce cycloalkenes from bio-based resources |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838201/ https://www.ncbi.nlm.nih.gov/pubmed/31699986 http://dx.doi.org/10.1038/s41467-019-13071-y |
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