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Organic–inorganic nanocrystal reductase to promote green asymmetric synthesis
An acetophenone reductase from Geotrichum candidum (GcAPRD) was immobilized by the organic–inorganic nanocrystal method. The GcAPRD nanocrystal presented improved stability and recyclability compared with those of the free GcAPRD. Moreover, the GcAPRD nanocrystal reduced broad kinds of ketones with...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056328/ https://www.ncbi.nlm.nih.gov/pubmed/35516042 http://dx.doi.org/10.1039/d0ra03160g |
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author | T.sriwong, Kotchakorn Koesoema, Afifa Ayu Matsuda, Tomoko |
author_facet | T.sriwong, Kotchakorn Koesoema, Afifa Ayu Matsuda, Tomoko |
author_sort | T.sriwong, Kotchakorn |
collection | PubMed |
description | An acetophenone reductase from Geotrichum candidum (GcAPRD) was immobilized by the organic–inorganic nanocrystal method. The GcAPRD nanocrystal presented improved stability and recyclability compared with those of the free GcAPRD. Moreover, the GcAPRD nanocrystal reduced broad kinds of ketones with excellent enantioselectivities to produce beneficial chiral alcohols such as (S)-1-(3′,4′-dichlorophenyl)ethanol with >99% yield and >99% ee. The robust and versatile properties of the GcAPRD nanocrystal demonstrated an approach to promote green asymmetric synthesis and sustainable chemistry. |
format | Online Article Text |
id | pubmed-9056328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90563282022-05-04 Organic–inorganic nanocrystal reductase to promote green asymmetric synthesis T.sriwong, Kotchakorn Koesoema, Afifa Ayu Matsuda, Tomoko RSC Adv Chemistry An acetophenone reductase from Geotrichum candidum (GcAPRD) was immobilized by the organic–inorganic nanocrystal method. The GcAPRD nanocrystal presented improved stability and recyclability compared with those of the free GcAPRD. Moreover, the GcAPRD nanocrystal reduced broad kinds of ketones with excellent enantioselectivities to produce beneficial chiral alcohols such as (S)-1-(3′,4′-dichlorophenyl)ethanol with >99% yield and >99% ee. The robust and versatile properties of the GcAPRD nanocrystal demonstrated an approach to promote green asymmetric synthesis and sustainable chemistry. The Royal Society of Chemistry 2020-08-20 /pmc/articles/PMC9056328/ /pubmed/35516042 http://dx.doi.org/10.1039/d0ra03160g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry T.sriwong, Kotchakorn Koesoema, Afifa Ayu Matsuda, Tomoko Organic–inorganic nanocrystal reductase to promote green asymmetric synthesis |
title | Organic–inorganic nanocrystal reductase to promote green asymmetric synthesis |
title_full | Organic–inorganic nanocrystal reductase to promote green asymmetric synthesis |
title_fullStr | Organic–inorganic nanocrystal reductase to promote green asymmetric synthesis |
title_full_unstemmed | Organic–inorganic nanocrystal reductase to promote green asymmetric synthesis |
title_short | Organic–inorganic nanocrystal reductase to promote green asymmetric synthesis |
title_sort | organic–inorganic nanocrystal reductase to promote green asymmetric synthesis |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056328/ https://www.ncbi.nlm.nih.gov/pubmed/35516042 http://dx.doi.org/10.1039/d0ra03160g |
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