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Strategies in megasynthase engineering – fatty acid synthases (FAS) as model proteins

Megasynthases are large multienzyme proteins that produce a plethora of important natural compounds by catalyzing the successive condensation and modification of precursor units. Within the class of megasynthases, polyketide synthases (PKS) are responsible for the production of a large spectrum of b...

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Autores principales: Fischer, Manuel, Grininger, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496573/
https://www.ncbi.nlm.nih.gov/pubmed/28694866
http://dx.doi.org/10.3762/bjoc.13.119
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author Fischer, Manuel
Grininger, Martin
author_facet Fischer, Manuel
Grininger, Martin
author_sort Fischer, Manuel
collection PubMed
description Megasynthases are large multienzyme proteins that produce a plethora of important natural compounds by catalyzing the successive condensation and modification of precursor units. Within the class of megasynthases, polyketide synthases (PKS) are responsible for the production of a large spectrum of bioactive polyketides (PK), which have frequently found their way into therapeutic applications. Rational engineering approaches have been performed during the last 25 years that seek to employ the “assembly-line synthetic concept” of megasynthases in order to deliver new bioactive compounds. Here, we highlight PKS engineering strategies in the light of the newly emerging structural information on megasynthases, and argue that fatty acid synthases (FAS) are and will be valuable objects for further developing this field.
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spelling pubmed-54965732017-07-10 Strategies in megasynthase engineering – fatty acid synthases (FAS) as model proteins Fischer, Manuel Grininger, Martin Beilstein J Org Chem Review Megasynthases are large multienzyme proteins that produce a plethora of important natural compounds by catalyzing the successive condensation and modification of precursor units. Within the class of megasynthases, polyketide synthases (PKS) are responsible for the production of a large spectrum of bioactive polyketides (PK), which have frequently found their way into therapeutic applications. Rational engineering approaches have been performed during the last 25 years that seek to employ the “assembly-line synthetic concept” of megasynthases in order to deliver new bioactive compounds. Here, we highlight PKS engineering strategies in the light of the newly emerging structural information on megasynthases, and argue that fatty acid synthases (FAS) are and will be valuable objects for further developing this field. Beilstein-Institut 2017-06-21 /pmc/articles/PMC5496573/ /pubmed/28694866 http://dx.doi.org/10.3762/bjoc.13.119 Text en Copyright © 2017, Fischer and Grininger 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
Fischer, Manuel
Grininger, Martin
Strategies in megasynthase engineering – fatty acid synthases (FAS) as model proteins
title Strategies in megasynthase engineering – fatty acid synthases (FAS) as model proteins
title_full Strategies in megasynthase engineering – fatty acid synthases (FAS) as model proteins
title_fullStr Strategies in megasynthase engineering – fatty acid synthases (FAS) as model proteins
title_full_unstemmed Strategies in megasynthase engineering – fatty acid synthases (FAS) as model proteins
title_short Strategies in megasynthase engineering – fatty acid synthases (FAS) as model proteins
title_sort strategies in megasynthase engineering – fatty acid synthases (fas) as model proteins
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496573/
https://www.ncbi.nlm.nih.gov/pubmed/28694866
http://dx.doi.org/10.3762/bjoc.13.119
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