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A synthetic cell-free 36-enzyme reaction system for vitamin B(12) production
Adenosylcobalamin (AdoCbl), a biologically active form of vitamin B(12) (coenzyme B(12)), is one of the most complex metal-containing natural compounds and an essential vitamin for animals. However, AdoCbl can only be de novo synthesized by prokaryotes, and its industrial manufacturing to date was l...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449867/ https://www.ncbi.nlm.nih.gov/pubmed/37620358 http://dx.doi.org/10.1038/s41467-023-40932-4 |
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author | Kang, Qian Fang, Huan Xiang, Mengjie Xiao, Kaixing Jiang, Pingtao You, Chun Lee, Sang Yup Zhang, Dawei |
author_facet | Kang, Qian Fang, Huan Xiang, Mengjie Xiao, Kaixing Jiang, Pingtao You, Chun Lee, Sang Yup Zhang, Dawei |
author_sort | Kang, Qian |
collection | PubMed |
description | Adenosylcobalamin (AdoCbl), a biologically active form of vitamin B(12) (coenzyme B(12)), is one of the most complex metal-containing natural compounds and an essential vitamin for animals. However, AdoCbl can only be de novo synthesized by prokaryotes, and its industrial manufacturing to date was limited to bacterial fermentation. Here, we report a method for the synthesis of AdoCbl based on a cell-free reaction system performing a cascade of catalytic reactions from 5-aminolevulinic acid (5-ALA), an inexpensive compound. More than 30 biocatalytic reactions are integrated and optimized to achieve the complete cell-free synthesis of AdoCbl, after overcoming feedback inhibition, the complicated detection, instability of intermediate products, as well as imbalance and competition of cofactors. In the end, this cell-free system produces 417.41 μg/L and 5.78 mg/L of AdoCbl using 5-ALA and the purified intermediate product hydrogenobyrate as substrates, respectively. The strategies of coordinating synthetic modules of complex cell-free system describe here will be generally useful for developing cell-free platforms to produce complex natural compounds with long and complicated biosynthetic pathways. |
format | Online Article Text |
id | pubmed-10449867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104498672023-08-26 A synthetic cell-free 36-enzyme reaction system for vitamin B(12) production Kang, Qian Fang, Huan Xiang, Mengjie Xiao, Kaixing Jiang, Pingtao You, Chun Lee, Sang Yup Zhang, Dawei Nat Commun Article Adenosylcobalamin (AdoCbl), a biologically active form of vitamin B(12) (coenzyme B(12)), is one of the most complex metal-containing natural compounds and an essential vitamin for animals. However, AdoCbl can only be de novo synthesized by prokaryotes, and its industrial manufacturing to date was limited to bacterial fermentation. Here, we report a method for the synthesis of AdoCbl based on a cell-free reaction system performing a cascade of catalytic reactions from 5-aminolevulinic acid (5-ALA), an inexpensive compound. More than 30 biocatalytic reactions are integrated and optimized to achieve the complete cell-free synthesis of AdoCbl, after overcoming feedback inhibition, the complicated detection, instability of intermediate products, as well as imbalance and competition of cofactors. In the end, this cell-free system produces 417.41 μg/L and 5.78 mg/L of AdoCbl using 5-ALA and the purified intermediate product hydrogenobyrate as substrates, respectively. The strategies of coordinating synthetic modules of complex cell-free system describe here will be generally useful for developing cell-free platforms to produce complex natural compounds with long and complicated biosynthetic pathways. Nature Publishing Group UK 2023-08-24 /pmc/articles/PMC10449867/ /pubmed/37620358 http://dx.doi.org/10.1038/s41467-023-40932-4 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kang, Qian Fang, Huan Xiang, Mengjie Xiao, Kaixing Jiang, Pingtao You, Chun Lee, Sang Yup Zhang, Dawei A synthetic cell-free 36-enzyme reaction system for vitamin B(12) production |
title | A synthetic cell-free 36-enzyme reaction system for vitamin B(12) production |
title_full | A synthetic cell-free 36-enzyme reaction system for vitamin B(12) production |
title_fullStr | A synthetic cell-free 36-enzyme reaction system for vitamin B(12) production |
title_full_unstemmed | A synthetic cell-free 36-enzyme reaction system for vitamin B(12) production |
title_short | A synthetic cell-free 36-enzyme reaction system for vitamin B(12) production |
title_sort | synthetic cell-free 36-enzyme reaction system for vitamin b(12) production |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449867/ https://www.ncbi.nlm.nih.gov/pubmed/37620358 http://dx.doi.org/10.1038/s41467-023-40932-4 |
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