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Influence of Cofactor Regeneration Strategies on Preparative-Scale, Asymmetric Carbonyl Reductions by Engineered Escherichia coli
[Image: see text] This study was designed to determine whether whole cells or crude enzyme extracts are more effective for preparative-scale ketone reductions by dehydrogenases as well as learning which cofactor regeneration scheme is most effective. Based on results from three representative ketone...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105172/ https://www.ncbi.nlm.nih.gov/pubmed/25067899 http://dx.doi.org/10.1021/op400312n |
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author | Dascier, Dimitri Kambourakis, Spiros Hua, Ling Rozzell, J. David Stewart, Jon D. |
author_facet | Dascier, Dimitri Kambourakis, Spiros Hua, Ling Rozzell, J. David Stewart, Jon D. |
author_sort | Dascier, Dimitri |
collection | PubMed |
description | [Image: see text] This study was designed to determine whether whole cells or crude enzyme extracts are more effective for preparative-scale ketone reductions by dehydrogenases as well as learning which cofactor regeneration scheme is most effective. Based on results from three representative ketone substrates (an α-fluoro-β-keto ester, a bis-trifluoromethylated acetophenone, and a symmetrical β-diketone), our results demonstrate that several nicotinamide cofactor regeneration strategies can be applied to preparative-scale dehydrogenase-catalyzed reactions successfully. |
format | Online Article Text |
id | pubmed-4105172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-41051722015-02-17 Influence of Cofactor Regeneration Strategies on Preparative-Scale, Asymmetric Carbonyl Reductions by Engineered Escherichia coli Dascier, Dimitri Kambourakis, Spiros Hua, Ling Rozzell, J. David Stewart, Jon D. Org Process Res Dev [Image: see text] This study was designed to determine whether whole cells or crude enzyme extracts are more effective for preparative-scale ketone reductions by dehydrogenases as well as learning which cofactor regeneration scheme is most effective. Based on results from three representative ketone substrates (an α-fluoro-β-keto ester, a bis-trifluoromethylated acetophenone, and a symmetrical β-diketone), our results demonstrate that several nicotinamide cofactor regeneration strategies can be applied to preparative-scale dehydrogenase-catalyzed reactions successfully. American Chemical Society 2014-02-17 2014-06-20 /pmc/articles/PMC4105172/ /pubmed/25067899 http://dx.doi.org/10.1021/op400312n Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Dascier, Dimitri Kambourakis, Spiros Hua, Ling Rozzell, J. David Stewart, Jon D. Influence of Cofactor Regeneration Strategies on Preparative-Scale, Asymmetric Carbonyl Reductions by Engineered Escherichia coli |
title | Influence
of Cofactor Regeneration Strategies on Preparative-Scale, Asymmetric
Carbonyl Reductions by Engineered Escherichia coli |
title_full | Influence
of Cofactor Regeneration Strategies on Preparative-Scale, Asymmetric
Carbonyl Reductions by Engineered Escherichia coli |
title_fullStr | Influence
of Cofactor Regeneration Strategies on Preparative-Scale, Asymmetric
Carbonyl Reductions by Engineered Escherichia coli |
title_full_unstemmed | Influence
of Cofactor Regeneration Strategies on Preparative-Scale, Asymmetric
Carbonyl Reductions by Engineered Escherichia coli |
title_short | Influence
of Cofactor Regeneration Strategies on Preparative-Scale, Asymmetric
Carbonyl Reductions by Engineered Escherichia coli |
title_sort | influence
of cofactor regeneration strategies on preparative-scale, asymmetric
carbonyl reductions by engineered escherichia coli |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105172/ https://www.ncbi.nlm.nih.gov/pubmed/25067899 http://dx.doi.org/10.1021/op400312n |
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