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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...

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Autores principales: Xu, Ruirui, Zhang, Weijao, Xi, Xintong, Chen, Jiamin, Wang, Yang, Du, Guocheng, Li, Jianghua, Chen, Jian, Kang, Zhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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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.
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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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