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Chemical Probes for the Functionalization of Polyketide Intermediates**

A library of functionalized chemical probes capable of reacting with ketosynthase-bound biosynthetic intermediates was prepared and utilized to explore in vivo polyketide diversification. Fermentation of ACP mutants of S. lasaliensis in the presence of the probes generated a range of unnatural polyk...

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Autores principales: Riva, Elena, Wilkening, Ina, Gazzola, Silvia, Li, W M Ariel, Smith, Luke, Leadlay, Peter F, Tosin, Manuela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4501312/
https://www.ncbi.nlm.nih.gov/pubmed/25212788
http://dx.doi.org/10.1002/anie.201407448
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author Riva, Elena
Wilkening, Ina
Gazzola, Silvia
Li, W M Ariel
Smith, Luke
Leadlay, Peter F
Tosin, Manuela
author_facet Riva, Elena
Wilkening, Ina
Gazzola, Silvia
Li, W M Ariel
Smith, Luke
Leadlay, Peter F
Tosin, Manuela
author_sort Riva, Elena
collection PubMed
description A library of functionalized chemical probes capable of reacting with ketosynthase-bound biosynthetic intermediates was prepared and utilized to explore in vivo polyketide diversification. Fermentation of ACP mutants of S. lasaliensis in the presence of the probes generated a range of unnatural polyketide derivatives, including novel putative lasalocid A derivatives characterized by variable aryl ketone moieties and linear polyketide chains (bearing alkyne/azide handles and fluorine) flanking the polyether scaffold. By providing direct information on microorganism tolerance and enzyme processing of unnatural malonyl-ACP analogues, as well as on the amenability of unnatural polyketides to further structural modifications, the chemical probes constitute invaluable tools for the development of novel mutasynthesis and synthetic biology.
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spelling pubmed-45013122015-07-21 Chemical Probes for the Functionalization of Polyketide Intermediates** Riva, Elena Wilkening, Ina Gazzola, Silvia Li, W M Ariel Smith, Luke Leadlay, Peter F Tosin, Manuela Angew Chem Int Ed Engl Communications A library of functionalized chemical probes capable of reacting with ketosynthase-bound biosynthetic intermediates was prepared and utilized to explore in vivo polyketide diversification. Fermentation of ACP mutants of S. lasaliensis in the presence of the probes generated a range of unnatural polyketide derivatives, including novel putative lasalocid A derivatives characterized by variable aryl ketone moieties and linear polyketide chains (bearing alkyne/azide handles and fluorine) flanking the polyether scaffold. By providing direct information on microorganism tolerance and enzyme processing of unnatural malonyl-ACP analogues, as well as on the amenability of unnatural polyketides to further structural modifications, the chemical probes constitute invaluable tools for the development of novel mutasynthesis and synthetic biology. WILEY-VCH Verlag 2014-10-27 2014-09-11 /pmc/articles/PMC4501312/ /pubmed/25212788 http://dx.doi.org/10.1002/anie.201407448 Text en © 2014 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited
spellingShingle Communications
Riva, Elena
Wilkening, Ina
Gazzola, Silvia
Li, W M Ariel
Smith, Luke
Leadlay, Peter F
Tosin, Manuela
Chemical Probes for the Functionalization of Polyketide Intermediates**
title Chemical Probes for the Functionalization of Polyketide Intermediates**
title_full Chemical Probes for the Functionalization of Polyketide Intermediates**
title_fullStr Chemical Probes for the Functionalization of Polyketide Intermediates**
title_full_unstemmed Chemical Probes for the Functionalization of Polyketide Intermediates**
title_short Chemical Probes for the Functionalization of Polyketide Intermediates**
title_sort chemical probes for the functionalization of polyketide intermediates**
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4501312/
https://www.ncbi.nlm.nih.gov/pubmed/25212788
http://dx.doi.org/10.1002/anie.201407448
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