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A Nonconventional Archaeal Fluorinase Identified by In Silico Mining for Enhanced Fluorine Biocatalysis
[Image: see text] Fluorinases, the only enzymes known to catalyze the transfer of fluorine to an organic molecule, are essential catalysts for the biological synthesis of valuable organofluorines. However, the few fluorinases identified so far have low turnover rates that hamper biotechnological app...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9173684/ https://www.ncbi.nlm.nih.gov/pubmed/35692250 http://dx.doi.org/10.1021/acscatal.2c01184 |
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author | Pardo, Isabel Bednar, David Calero, Patricia Volke, Daniel C. Damborský, Jiří Nikel, Pablo I. |
author_facet | Pardo, Isabel Bednar, David Calero, Patricia Volke, Daniel C. Damborský, Jiří Nikel, Pablo I. |
author_sort | Pardo, Isabel |
collection | PubMed |
description | [Image: see text] Fluorinases, the only enzymes known to catalyze the transfer of fluorine to an organic molecule, are essential catalysts for the biological synthesis of valuable organofluorines. However, the few fluorinases identified so far have low turnover rates that hamper biotechnological applications. Here, we isolated and characterized putative fluorinases retrieved from systematic in silico mining and identified a nonconventional archaeal enzyme from Methanosaeta sp. that mediates the fastest S(N)2 fluorination rate reported to date. Furthermore, we demonstrate enhanced production of fluoronucleotides in vivo in a bacterial host engineered with this archaeal fluorinase, paving the way toward synthetic metabolism for efficient biohalogenation. |
format | Online Article Text |
id | pubmed-9173684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-91736842022-06-08 A Nonconventional Archaeal Fluorinase Identified by In Silico Mining for Enhanced Fluorine Biocatalysis Pardo, Isabel Bednar, David Calero, Patricia Volke, Daniel C. Damborský, Jiří Nikel, Pablo I. ACS Catal [Image: see text] Fluorinases, the only enzymes known to catalyze the transfer of fluorine to an organic molecule, are essential catalysts for the biological synthesis of valuable organofluorines. However, the few fluorinases identified so far have low turnover rates that hamper biotechnological applications. Here, we isolated and characterized putative fluorinases retrieved from systematic in silico mining and identified a nonconventional archaeal enzyme from Methanosaeta sp. that mediates the fastest S(N)2 fluorination rate reported to date. Furthermore, we demonstrate enhanced production of fluoronucleotides in vivo in a bacterial host engineered with this archaeal fluorinase, paving the way toward synthetic metabolism for efficient biohalogenation. American Chemical Society 2022-05-19 2022-06-03 /pmc/articles/PMC9173684/ /pubmed/35692250 http://dx.doi.org/10.1021/acscatal.2c01184 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Pardo, Isabel Bednar, David Calero, Patricia Volke, Daniel C. Damborský, Jiří Nikel, Pablo I. A Nonconventional Archaeal Fluorinase Identified by In Silico Mining for Enhanced Fluorine Biocatalysis |
title | A Nonconventional Archaeal Fluorinase Identified by
In Silico Mining for Enhanced Fluorine Biocatalysis |
title_full | A Nonconventional Archaeal Fluorinase Identified by
In Silico Mining for Enhanced Fluorine Biocatalysis |
title_fullStr | A Nonconventional Archaeal Fluorinase Identified by
In Silico Mining for Enhanced Fluorine Biocatalysis |
title_full_unstemmed | A Nonconventional Archaeal Fluorinase Identified by
In Silico Mining for Enhanced Fluorine Biocatalysis |
title_short | A Nonconventional Archaeal Fluorinase Identified by
In Silico Mining for Enhanced Fluorine Biocatalysis |
title_sort | nonconventional archaeal fluorinase identified by
in silico mining for enhanced fluorine biocatalysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9173684/ https://www.ncbi.nlm.nih.gov/pubmed/35692250 http://dx.doi.org/10.1021/acscatal.2c01184 |
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