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Polyketide stereocontrol: a study in chemical biology
The biosynthesis of reduced polyketides in bacteria by modular polyketide synthases (PKSs) proceeds with exquisite stereocontrol. As the stereochemistry is intimately linked to the strong bioactivity of these molecules, the origins of stereochemical control are of significant interest in attempts to...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Beilstein-Institut
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331325/ https://www.ncbi.nlm.nih.gov/pubmed/28326145 http://dx.doi.org/10.3762/bjoc.13.39 |
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author | Weissman, Kira J |
author_facet | Weissman, Kira J |
author_sort | Weissman, Kira J |
collection | PubMed |
description | The biosynthesis of reduced polyketides in bacteria by modular polyketide synthases (PKSs) proceeds with exquisite stereocontrol. As the stereochemistry is intimately linked to the strong bioactivity of these molecules, the origins of stereochemical control are of significant interest in attempts to create derivatives of these compounds by genetic engineering. In this review, we discuss the current state of knowledge regarding this key aspect of the biosynthetic pathways. Given that much of this information has been obtained using chemical biology tools, work in this area serves as a showcase for the power of this approach to provide answers to fundamental biological questions. |
format | Online Article Text |
id | pubmed-5331325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-53313252017-03-21 Polyketide stereocontrol: a study in chemical biology Weissman, Kira J Beilstein J Org Chem Review The biosynthesis of reduced polyketides in bacteria by modular polyketide synthases (PKSs) proceeds with exquisite stereocontrol. As the stereochemistry is intimately linked to the strong bioactivity of these molecules, the origins of stereochemical control are of significant interest in attempts to create derivatives of these compounds by genetic engineering. In this review, we discuss the current state of knowledge regarding this key aspect of the biosynthetic pathways. Given that much of this information has been obtained using chemical biology tools, work in this area serves as a showcase for the power of this approach to provide answers to fundamental biological questions. Beilstein-Institut 2017-02-24 /pmc/articles/PMC5331325/ /pubmed/28326145 http://dx.doi.org/10.3762/bjoc.13.39 Text en Copyright © 2017, Weissman https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Review Weissman, Kira J Polyketide stereocontrol: a study in chemical biology |
title | Polyketide stereocontrol: a study in chemical biology |
title_full | Polyketide stereocontrol: a study in chemical biology |
title_fullStr | Polyketide stereocontrol: a study in chemical biology |
title_full_unstemmed | Polyketide stereocontrol: a study in chemical biology |
title_short | Polyketide stereocontrol: a study in chemical biology |
title_sort | polyketide stereocontrol: a study in chemical biology |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331325/ https://www.ncbi.nlm.nih.gov/pubmed/28326145 http://dx.doi.org/10.3762/bjoc.13.39 |
work_keys_str_mv | AT weissmankiraj polyketidestereocontrolastudyinchemicalbiology |