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Engineering sulfonate group donor regeneration systems to boost biosynthesis of sulfated compounds
Sulfonation as one of the most important modification reactions in nature is essential for many biological macromolecules to function. Development of green sulfonate group donor regeneration systems to efficiently sulfonate compounds of interest is always attractive. Here, we design and engineer two...
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/PMC10638397/ https://www.ncbi.nlm.nih.gov/pubmed/37949843 http://dx.doi.org/10.1038/s41467-023-43195-1 |
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author | Xu, Ruirui Zhang, Weijao Xi, Xintong Chen, Jiamin Wang, Yang Du, Guocheng Li, Jianghua Chen, Jian Kang, Zhen |
author_facet | Xu, Ruirui Zhang, Weijao Xi, Xintong Chen, Jiamin Wang, Yang Du, Guocheng Li, Jianghua Chen, Jian Kang, Zhen |
author_sort | Xu, Ruirui |
collection | PubMed |
description | Sulfonation as one of the most important modification reactions in nature is essential for many biological macromolecules to function. Development of green sulfonate group donor regeneration systems to efficiently sulfonate compounds of interest is always attractive. Here, we design and engineer two different sulfonate group donor regeneration systems to boost the biosynthesis of sulfated compounds. First, we assemble three modules to construct a 3'-phosphoadenosine-5'-phosphosulfate (PAPS) regeneration system and demonstrate its applicability for living cells. After discovering adenosine 5’-phosphosulfate (APS) as another active sulfonate group donor, we engineer a more simplified APS regeneration system that couples specific sulfotransferase. Next, we develop a rapid indicating system for characterizing the activity of APS-mediated sulfotransferase to rapidly screen sulfotransferase variants with increased activity towards APS. Eventually, the active sulfonate group equivalent values of the APS regeneration systems towards trehalose and p-coumaric acid reach 3.26 and 4.03, respectively. The present PAPS and APS regeneration systems are environmentally friendly and applicable for scaling up the biomanufacturing of sulfated products. |
format | Online Article Text |
id | pubmed-10638397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106383972023-11-11 Engineering sulfonate group donor regeneration systems to boost biosynthesis of sulfated compounds Xu, Ruirui Zhang, Weijao Xi, Xintong Chen, Jiamin Wang, Yang Du, Guocheng Li, Jianghua Chen, Jian Kang, Zhen Nat Commun Article Sulfonation as one of the most important modification reactions in nature is essential for many biological macromolecules to function. Development of green sulfonate group donor regeneration systems to efficiently sulfonate compounds of interest is always attractive. Here, we design and engineer two different sulfonate group donor regeneration systems to boost the biosynthesis of sulfated compounds. First, we assemble three modules to construct a 3'-phosphoadenosine-5'-phosphosulfate (PAPS) regeneration system and demonstrate its applicability for living cells. After discovering adenosine 5’-phosphosulfate (APS) as another active sulfonate group donor, we engineer a more simplified APS regeneration system that couples specific sulfotransferase. Next, we develop a rapid indicating system for characterizing the activity of APS-mediated sulfotransferase to rapidly screen sulfotransferase variants with increased activity towards APS. Eventually, the active sulfonate group equivalent values of the APS regeneration systems towards trehalose and p-coumaric acid reach 3.26 and 4.03, respectively. The present PAPS and APS regeneration systems are environmentally friendly and applicable for scaling up the biomanufacturing of sulfated products. Nature Publishing Group UK 2023-11-10 /pmc/articles/PMC10638397/ /pubmed/37949843 http://dx.doi.org/10.1038/s41467-023-43195-1 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 Xu, Ruirui Zhang, Weijao Xi, Xintong Chen, Jiamin Wang, Yang Du, Guocheng Li, Jianghua Chen, Jian Kang, Zhen Engineering sulfonate group donor regeneration systems to boost biosynthesis of sulfated compounds |
title | Engineering sulfonate group donor regeneration systems to boost biosynthesis of sulfated compounds |
title_full | Engineering sulfonate group donor regeneration systems to boost biosynthesis of sulfated compounds |
title_fullStr | Engineering sulfonate group donor regeneration systems to boost biosynthesis of sulfated compounds |
title_full_unstemmed | Engineering sulfonate group donor regeneration systems to boost biosynthesis of sulfated compounds |
title_short | Engineering sulfonate group donor regeneration systems to boost biosynthesis of sulfated compounds |
title_sort | engineering sulfonate group donor regeneration systems to boost biosynthesis of sulfated compounds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10638397/ https://www.ncbi.nlm.nih.gov/pubmed/37949843 http://dx.doi.org/10.1038/s41467-023-43195-1 |
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