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A tripartite microbial co-culture system for de novo biosynthesis of diverse plant phenylpropanoids
Plant-derived phenylpropanoids, in particular phenylpropenes, have diverse industrial applications ranging from flavors and fragrances to polymers and pharmaceuticals. Heterologous biosynthesis of these products has the potential to address low, seasonally dependent yields hindering ease of widespre...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10366228/ https://www.ncbi.nlm.nih.gov/pubmed/37488111 http://dx.doi.org/10.1038/s41467-023-40242-9 |
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author | Brooks, Sierra M. Marsan, Celeste Reed, Kevin B. Yuan, Shuo-Fu Nguyen, Dustin-Dat Trivedi, Adit Altin-Yavuzarslan, Gokce Ballinger, Nathan Nelson, Alshakim Alper, Hal S. |
author_facet | Brooks, Sierra M. Marsan, Celeste Reed, Kevin B. Yuan, Shuo-Fu Nguyen, Dustin-Dat Trivedi, Adit Altin-Yavuzarslan, Gokce Ballinger, Nathan Nelson, Alshakim Alper, Hal S. |
author_sort | Brooks, Sierra M. |
collection | PubMed |
description | Plant-derived phenylpropanoids, in particular phenylpropenes, have diverse industrial applications ranging from flavors and fragrances to polymers and pharmaceuticals. Heterologous biosynthesis of these products has the potential to address low, seasonally dependent yields hindering ease of widespread manufacturing. However, previous efforts have been hindered by the inherent pathway promiscuity and the microbial toxicity of key pathway intermediates. Here, in this study, we establish the propensity of a tripartite microbial co-culture to overcome these limitations and demonstrate to our knowledge the first reported de novo phenylpropene production from simple sugar starting materials. After initially designing the system to accumulate eugenol, the platform modularity and downstream enzyme promiscuity was leveraged to quickly create avenues for hydroxychavicol and chavicol production. The consortia was found to be compatible with Engineered Living Material production platforms that allow for reusable, cold-chain-independent distributed manufacturing. This work lays the foundation for further deployment of modular microbial approaches to produce plant secondary metabolites. |
format | Online Article Text |
id | pubmed-10366228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103662282023-07-26 A tripartite microbial co-culture system for de novo biosynthesis of diverse plant phenylpropanoids Brooks, Sierra M. Marsan, Celeste Reed, Kevin B. Yuan, Shuo-Fu Nguyen, Dustin-Dat Trivedi, Adit Altin-Yavuzarslan, Gokce Ballinger, Nathan Nelson, Alshakim Alper, Hal S. Nat Commun Article Plant-derived phenylpropanoids, in particular phenylpropenes, have diverse industrial applications ranging from flavors and fragrances to polymers and pharmaceuticals. Heterologous biosynthesis of these products has the potential to address low, seasonally dependent yields hindering ease of widespread manufacturing. However, previous efforts have been hindered by the inherent pathway promiscuity and the microbial toxicity of key pathway intermediates. Here, in this study, we establish the propensity of a tripartite microbial co-culture to overcome these limitations and demonstrate to our knowledge the first reported de novo phenylpropene production from simple sugar starting materials. After initially designing the system to accumulate eugenol, the platform modularity and downstream enzyme promiscuity was leveraged to quickly create avenues for hydroxychavicol and chavicol production. The consortia was found to be compatible with Engineered Living Material production platforms that allow for reusable, cold-chain-independent distributed manufacturing. This work lays the foundation for further deployment of modular microbial approaches to produce plant secondary metabolites. Nature Publishing Group UK 2023-07-24 /pmc/articles/PMC10366228/ /pubmed/37488111 http://dx.doi.org/10.1038/s41467-023-40242-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Brooks, Sierra M. Marsan, Celeste Reed, Kevin B. Yuan, Shuo-Fu Nguyen, Dustin-Dat Trivedi, Adit Altin-Yavuzarslan, Gokce Ballinger, Nathan Nelson, Alshakim Alper, Hal S. A tripartite microbial co-culture system for de novo biosynthesis of diverse plant phenylpropanoids |
title | A tripartite microbial co-culture system for de novo biosynthesis of diverse plant phenylpropanoids |
title_full | A tripartite microbial co-culture system for de novo biosynthesis of diverse plant phenylpropanoids |
title_fullStr | A tripartite microbial co-culture system for de novo biosynthesis of diverse plant phenylpropanoids |
title_full_unstemmed | A tripartite microbial co-culture system for de novo biosynthesis of diverse plant phenylpropanoids |
title_short | A tripartite microbial co-culture system for de novo biosynthesis of diverse plant phenylpropanoids |
title_sort | tripartite microbial co-culture system for de novo biosynthesis of diverse plant phenylpropanoids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10366228/ https://www.ncbi.nlm.nih.gov/pubmed/37488111 http://dx.doi.org/10.1038/s41467-023-40242-9 |
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