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Hydrogenase-based oxidative biocatalysis without oxygen
Biocatalysis-based synthesis can provide a sustainable and clean platform for producing chemicals. Many oxidative biocatalytic routes require the cofactor NAD(+) as an electron acceptor. To date, NADH oxidase (NOX) remains the most widely applied system for NAD(+) regeneration. However, its dependen...
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/PMC10232426/ https://www.ncbi.nlm.nih.gov/pubmed/37258512 http://dx.doi.org/10.1038/s41467-023-38227-9 |
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author | Al-Shameri, Ammar Siebert, Dominik L. Sutiono, Samuel Lauterbach, Lars Sieber, Volker |
author_facet | Al-Shameri, Ammar Siebert, Dominik L. Sutiono, Samuel Lauterbach, Lars Sieber, Volker |
author_sort | Al-Shameri, Ammar |
collection | PubMed |
description | Biocatalysis-based synthesis can provide a sustainable and clean platform for producing chemicals. Many oxidative biocatalytic routes require the cofactor NAD(+) as an electron acceptor. To date, NADH oxidase (NOX) remains the most widely applied system for NAD(+) regeneration. However, its dependence on O(2) implies various technical challenges in terms of O(2) supply, solubility, and mass transfer. Here, we present the suitability of a NAD(+) regeneration system in vitro based on H(2) evolution. The efficiency of the hydrogenase-based system is demonstrated by integrating it into a multi-enzymatic cascade to produce ketoacids from sugars. The total NAD(+) recycled using the hydrogenase system outperforms NOX in all different setups reaching up to 44,000 mol per mol enzyme. This system proves to be scalable and superior to NOX in terms of technical simplicity, flexibility, and total output. Furthermore, the system produces only green H(2) as a by-product even in the presence of O(2). |
format | Online Article Text |
id | pubmed-10232426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102324262023-06-02 Hydrogenase-based oxidative biocatalysis without oxygen Al-Shameri, Ammar Siebert, Dominik L. Sutiono, Samuel Lauterbach, Lars Sieber, Volker Nat Commun Article Biocatalysis-based synthesis can provide a sustainable and clean platform for producing chemicals. Many oxidative biocatalytic routes require the cofactor NAD(+) as an electron acceptor. To date, NADH oxidase (NOX) remains the most widely applied system for NAD(+) regeneration. However, its dependence on O(2) implies various technical challenges in terms of O(2) supply, solubility, and mass transfer. Here, we present the suitability of a NAD(+) regeneration system in vitro based on H(2) evolution. The efficiency of the hydrogenase-based system is demonstrated by integrating it into a multi-enzymatic cascade to produce ketoacids from sugars. The total NAD(+) recycled using the hydrogenase system outperforms NOX in all different setups reaching up to 44,000 mol per mol enzyme. This system proves to be scalable and superior to NOX in terms of technical simplicity, flexibility, and total output. Furthermore, the system produces only green H(2) as a by-product even in the presence of O(2). Nature Publishing Group UK 2023-05-31 /pmc/articles/PMC10232426/ /pubmed/37258512 http://dx.doi.org/10.1038/s41467-023-38227-9 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 Al-Shameri, Ammar Siebert, Dominik L. Sutiono, Samuel Lauterbach, Lars Sieber, Volker Hydrogenase-based oxidative biocatalysis without oxygen |
title | Hydrogenase-based oxidative biocatalysis without oxygen |
title_full | Hydrogenase-based oxidative biocatalysis without oxygen |
title_fullStr | Hydrogenase-based oxidative biocatalysis without oxygen |
title_full_unstemmed | Hydrogenase-based oxidative biocatalysis without oxygen |
title_short | Hydrogenase-based oxidative biocatalysis without oxygen |
title_sort | hydrogenase-based oxidative biocatalysis without oxygen |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10232426/ https://www.ncbi.nlm.nih.gov/pubmed/37258512 http://dx.doi.org/10.1038/s41467-023-38227-9 |
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