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RadH: A Versatile Halogenase for Integration into Synthetic Pathways

Flavin‐dependent halogenases are useful enzymes for providing halogenated molecules with improved biological activity, or intermediates for synthetic derivatization. We demonstrate how the fungal halogenase RadH can be used to regioselectively halogenate a range of bioactive aromatic scaffolds. Site...

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Autores principales: Menon, Binuraj R. K., Brandenburger, Eileen, Sharif, Humera H., Klemstein, Ulrike, Shepherd, Sarah A., Greaney, Michael F., Micklefield, Jason
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5637929/
https://www.ncbi.nlm.nih.gov/pubmed/28722773
http://dx.doi.org/10.1002/anie.201706342
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author Menon, Binuraj R. K.
Brandenburger, Eileen
Sharif, Humera H.
Klemstein, Ulrike
Shepherd, Sarah A.
Greaney, Michael F.
Micklefield, Jason
author_facet Menon, Binuraj R. K.
Brandenburger, Eileen
Sharif, Humera H.
Klemstein, Ulrike
Shepherd, Sarah A.
Greaney, Michael F.
Micklefield, Jason
author_sort Menon, Binuraj R. K.
collection PubMed
description Flavin‐dependent halogenases are useful enzymes for providing halogenated molecules with improved biological activity, or intermediates for synthetic derivatization. We demonstrate how the fungal halogenase RadH can be used to regioselectively halogenate a range of bioactive aromatic scaffolds. Site‐directed mutagenesis of RadH was used to identify catalytic residues and provide insight into the mechanism of fungal halogenases. A high‐throughput fluorescence screen was also developed, which enabled a RadH mutant to be evolved with improved properties. Finally we demonstrate how biosynthetic genes from fungi, bacteria, and plants can be combined to encode a new pathway to generate a novel chlorinated coumarin “non‐natural” product in E. coli.
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spelling pubmed-56379292017-10-25 RadH: A Versatile Halogenase for Integration into Synthetic Pathways Menon, Binuraj R. K. Brandenburger, Eileen Sharif, Humera H. Klemstein, Ulrike Shepherd, Sarah A. Greaney, Michael F. Micklefield, Jason Angew Chem Int Ed Engl Communications Flavin‐dependent halogenases are useful enzymes for providing halogenated molecules with improved biological activity, or intermediates for synthetic derivatization. We demonstrate how the fungal halogenase RadH can be used to regioselectively halogenate a range of bioactive aromatic scaffolds. Site‐directed mutagenesis of RadH was used to identify catalytic residues and provide insight into the mechanism of fungal halogenases. A high‐throughput fluorescence screen was also developed, which enabled a RadH mutant to be evolved with improved properties. Finally we demonstrate how biosynthetic genes from fungi, bacteria, and plants can be combined to encode a new pathway to generate a novel chlorinated coumarin “non‐natural” product in E. coli. John Wiley and Sons Inc. 2017-08-18 2017-09-18 /pmc/articles/PMC5637929/ /pubmed/28722773 http://dx.doi.org/10.1002/anie.201706342 Text en © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Menon, Binuraj R. K.
Brandenburger, Eileen
Sharif, Humera H.
Klemstein, Ulrike
Shepherd, Sarah A.
Greaney, Michael F.
Micklefield, Jason
RadH: A Versatile Halogenase for Integration into Synthetic Pathways
title RadH: A Versatile Halogenase for Integration into Synthetic Pathways
title_full RadH: A Versatile Halogenase for Integration into Synthetic Pathways
title_fullStr RadH: A Versatile Halogenase for Integration into Synthetic Pathways
title_full_unstemmed RadH: A Versatile Halogenase for Integration into Synthetic Pathways
title_short RadH: A Versatile Halogenase for Integration into Synthetic Pathways
title_sort radh: a versatile halogenase for integration into synthetic pathways
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5637929/
https://www.ncbi.nlm.nih.gov/pubmed/28722773
http://dx.doi.org/10.1002/anie.201706342
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