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Development of Continuous Flow Systems to Access Secondary Amines Through Previously Incompatible Biocatalytic Cascades
A key aim of biocatalysis is to mimic the ability of eukaryotic cells to carry out multistep cascades in a controlled and selective way. As biocatalytic cascades get more complex, reactions become unattainable under typical batch conditions. Here a number of continuous flow systems were used to over...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8453870/ https://www.ncbi.nlm.nih.gov/pubmed/33856106 http://dx.doi.org/10.1002/anie.202103805 |
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author | Mattey, Ashley P. Ford, Grayson J. Citoler, Joan Baldwin, Christopher Marshall, James R. Palmer, Ryan B. Thompson, Matthew Turner, Nicholas J. Cosgrove, Sebastian C. Flitsch, Sabine L. |
author_facet | Mattey, Ashley P. Ford, Grayson J. Citoler, Joan Baldwin, Christopher Marshall, James R. Palmer, Ryan B. Thompson, Matthew Turner, Nicholas J. Cosgrove, Sebastian C. Flitsch, Sabine L. |
author_sort | Mattey, Ashley P. |
collection | PubMed |
description | A key aim of biocatalysis is to mimic the ability of eukaryotic cells to carry out multistep cascades in a controlled and selective way. As biocatalytic cascades get more complex, reactions become unattainable under typical batch conditions. Here a number of continuous flow systems were used to overcome batch incompatibility, thus allowing for successful biocatalytic cascades. As proof‐of‐principle, reactive carbonyl intermediates were generated in situ using alcohol oxidases, then passed directly to a series of packed‐bed modules containing different aminating biocatalysts which accordingly produced a range of structurally distinct amines. The method was expanded to employ a batch incompatible sequential amination cascade via an oxidase/transaminase/imine reductase sequence, introducing different amine reagents at each step without cross‐reactivity. The combined approaches allowed for the biocatalytic synthesis of the natural product 4O‐methylnorbelladine. |
format | Online Article Text |
id | pubmed-8453870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84538702021-09-27 Development of Continuous Flow Systems to Access Secondary Amines Through Previously Incompatible Biocatalytic Cascades Mattey, Ashley P. Ford, Grayson J. Citoler, Joan Baldwin, Christopher Marshall, James R. Palmer, Ryan B. Thompson, Matthew Turner, Nicholas J. Cosgrove, Sebastian C. Flitsch, Sabine L. Angew Chem Int Ed Engl Research Articles A key aim of biocatalysis is to mimic the ability of eukaryotic cells to carry out multistep cascades in a controlled and selective way. As biocatalytic cascades get more complex, reactions become unattainable under typical batch conditions. Here a number of continuous flow systems were used to overcome batch incompatibility, thus allowing for successful biocatalytic cascades. As proof‐of‐principle, reactive carbonyl intermediates were generated in situ using alcohol oxidases, then passed directly to a series of packed‐bed modules containing different aminating biocatalysts which accordingly produced a range of structurally distinct amines. The method was expanded to employ a batch incompatible sequential amination cascade via an oxidase/transaminase/imine reductase sequence, introducing different amine reagents at each step without cross‐reactivity. The combined approaches allowed for the biocatalytic synthesis of the natural product 4O‐methylnorbelladine. John Wiley and Sons Inc. 2021-05-19 2021-08-16 /pmc/articles/PMC8453870/ /pubmed/33856106 http://dx.doi.org/10.1002/anie.202103805 Text en © 2021 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Mattey, Ashley P. Ford, Grayson J. Citoler, Joan Baldwin, Christopher Marshall, James R. Palmer, Ryan B. Thompson, Matthew Turner, Nicholas J. Cosgrove, Sebastian C. Flitsch, Sabine L. Development of Continuous Flow Systems to Access Secondary Amines Through Previously Incompatible Biocatalytic Cascades |
title | Development of Continuous Flow Systems to Access Secondary Amines Through Previously Incompatible Biocatalytic Cascades
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title_full | Development of Continuous Flow Systems to Access Secondary Amines Through Previously Incompatible Biocatalytic Cascades
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title_fullStr | Development of Continuous Flow Systems to Access Secondary Amines Through Previously Incompatible Biocatalytic Cascades
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title_full_unstemmed | Development of Continuous Flow Systems to Access Secondary Amines Through Previously Incompatible Biocatalytic Cascades
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title_short | Development of Continuous Flow Systems to Access Secondary Amines Through Previously Incompatible Biocatalytic Cascades
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title_sort | development of continuous flow systems to access secondary amines through previously incompatible biocatalytic cascades |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8453870/ https://www.ncbi.nlm.nih.gov/pubmed/33856106 http://dx.doi.org/10.1002/anie.202103805 |
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