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Three Steps, Two Enzymes, One Pot, but a Multitude of Nanocompartments: Combined Cycles of Kinetic Resolutions and Re-racemization with Incompatible Biocatalysts
[Image: see text] Deracemizations are clearly preferable to kinetic resolutions in the production of chiral molecules from racemates, as they allow up to 100% chemical and optical yield. Here we present a new process route for multienzymatic deracemizations that is relevant for reaction systems with...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567398/ https://www.ncbi.nlm.nih.gov/pubmed/34746608 http://dx.doi.org/10.1021/acsomega.1c04694 |
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author | Golombek, Florian Haumann, Marco Knoll, Matthias S.G. Fröba, Andreas Paul Castiglione, Kathrin |
author_facet | Golombek, Florian Haumann, Marco Knoll, Matthias S.G. Fröba, Andreas Paul Castiglione, Kathrin |
author_sort | Golombek, Florian |
collection | PubMed |
description | [Image: see text] Deracemizations are clearly preferable to kinetic resolutions in the production of chiral molecules from racemates, as they allow up to 100% chemical and optical yield. Here we present a new process route for multienzymatic deracemizations that is relevant for reaction systems with incompatible reaction conditions of the biocatalysts. This often applies to combinations of lipases used for stereoselective acylation and solvent-sensitive racemases. By encapsulating a model racemase in polymeric vesicles, it was protected from inactivation by the organic solvent up to phase proportions of 99%. As high yields in the lipase reaction required either water proportions well below 1% or racemase-denaturating acyl donor concentrations, a one-pot reaction was implemented through the sequential use of lipase and racemase-containing nanocompartments. This strategy allowed us to perform two kinetic resolutions with intermittent re-racemization in one pot yielding 72% (0.72 mM after 120 h) of an enantiopure product. |
format | Online Article Text |
id | pubmed-8567398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-85673982021-11-05 Three Steps, Two Enzymes, One Pot, but a Multitude of Nanocompartments: Combined Cycles of Kinetic Resolutions and Re-racemization with Incompatible Biocatalysts Golombek, Florian Haumann, Marco Knoll, Matthias S.G. Fröba, Andreas Paul Castiglione, Kathrin ACS Omega [Image: see text] Deracemizations are clearly preferable to kinetic resolutions in the production of chiral molecules from racemates, as they allow up to 100% chemical and optical yield. Here we present a new process route for multienzymatic deracemizations that is relevant for reaction systems with incompatible reaction conditions of the biocatalysts. This often applies to combinations of lipases used for stereoselective acylation and solvent-sensitive racemases. By encapsulating a model racemase in polymeric vesicles, it was protected from inactivation by the organic solvent up to phase proportions of 99%. As high yields in the lipase reaction required either water proportions well below 1% or racemase-denaturating acyl donor concentrations, a one-pot reaction was implemented through the sequential use of lipase and racemase-containing nanocompartments. This strategy allowed us to perform two kinetic resolutions with intermittent re-racemization in one pot yielding 72% (0.72 mM after 120 h) of an enantiopure product. American Chemical Society 2021-10-21 /pmc/articles/PMC8567398/ /pubmed/34746608 http://dx.doi.org/10.1021/acsomega.1c04694 Text en © 2021 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 | Golombek, Florian Haumann, Marco Knoll, Matthias S.G. Fröba, Andreas Paul Castiglione, Kathrin Three Steps, Two Enzymes, One Pot, but a Multitude of Nanocompartments: Combined Cycles of Kinetic Resolutions and Re-racemization with Incompatible Biocatalysts |
title | Three Steps, Two Enzymes, One Pot, but a Multitude
of Nanocompartments: Combined Cycles of Kinetic Resolutions and Re-racemization
with Incompatible Biocatalysts |
title_full | Three Steps, Two Enzymes, One Pot, but a Multitude
of Nanocompartments: Combined Cycles of Kinetic Resolutions and Re-racemization
with Incompatible Biocatalysts |
title_fullStr | Three Steps, Two Enzymes, One Pot, but a Multitude
of Nanocompartments: Combined Cycles of Kinetic Resolutions and Re-racemization
with Incompatible Biocatalysts |
title_full_unstemmed | Three Steps, Two Enzymes, One Pot, but a Multitude
of Nanocompartments: Combined Cycles of Kinetic Resolutions and Re-racemization
with Incompatible Biocatalysts |
title_short | Three Steps, Two Enzymes, One Pot, but a Multitude
of Nanocompartments: Combined Cycles of Kinetic Resolutions and Re-racemization
with Incompatible Biocatalysts |
title_sort | three steps, two enzymes, one pot, but a multitude
of nanocompartments: combined cycles of kinetic resolutions and re-racemization
with incompatible biocatalysts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567398/ https://www.ncbi.nlm.nih.gov/pubmed/34746608 http://dx.doi.org/10.1021/acsomega.1c04694 |
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