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In vitro studies of maleidride-forming enzymes

In vitro assays of enzymes involved in the biosynthesis of maleidrides from polyketides in fungi were performed. The results show that the enzymes are closely related to primary metabolism enzymes of the citric acid cycle in terms of stereochemical preferences, but with an expanded substrate selecti...

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Detalles Bibliográficos
Autores principales: Yin, Sen, Friedrich, Steffen, Hrupins, Vjaceslavs, Cox, Russell J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697804/
https://www.ncbi.nlm.nih.gov/pubmed/35424071
http://dx.doi.org/10.1039/d1ra02118d
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author Yin, Sen
Friedrich, Steffen
Hrupins, Vjaceslavs
Cox, Russell J.
author_facet Yin, Sen
Friedrich, Steffen
Hrupins, Vjaceslavs
Cox, Russell J.
author_sort Yin, Sen
collection PubMed
description In vitro assays of enzymes involved in the biosynthesis of maleidrides from polyketides in fungi were performed. The results show that the enzymes are closely related to primary metabolism enzymes of the citric acid cycle in terms of stereochemical preferences, but with an expanded substrate selectivity. A key citrate synthase can react both saturated and unsaturated acyl CoA substrates to give solely anti substituted citrates. This undergoes anti-dehydration to afford an unsaturated precursor which is cyclised in vitro by ketosteroid-isomerase-like enzymes to give byssochlamic acid.
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spelling pubmed-86978042022-04-13 In vitro studies of maleidride-forming enzymes Yin, Sen Friedrich, Steffen Hrupins, Vjaceslavs Cox, Russell J. RSC Adv Chemistry In vitro assays of enzymes involved in the biosynthesis of maleidrides from polyketides in fungi were performed. The results show that the enzymes are closely related to primary metabolism enzymes of the citric acid cycle in terms of stereochemical preferences, but with an expanded substrate selectivity. A key citrate synthase can react both saturated and unsaturated acyl CoA substrates to give solely anti substituted citrates. This undergoes anti-dehydration to afford an unsaturated precursor which is cyclised in vitro by ketosteroid-isomerase-like enzymes to give byssochlamic acid. The Royal Society of Chemistry 2021-04-21 /pmc/articles/PMC8697804/ /pubmed/35424071 http://dx.doi.org/10.1039/d1ra02118d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Yin, Sen
Friedrich, Steffen
Hrupins, Vjaceslavs
Cox, Russell J.
In vitro studies of maleidride-forming enzymes
title In vitro studies of maleidride-forming enzymes
title_full In vitro studies of maleidride-forming enzymes
title_fullStr In vitro studies of maleidride-forming enzymes
title_full_unstemmed In vitro studies of maleidride-forming enzymes
title_short In vitro studies of maleidride-forming enzymes
title_sort in vitro studies of maleidride-forming enzymes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697804/
https://www.ncbi.nlm.nih.gov/pubmed/35424071
http://dx.doi.org/10.1039/d1ra02118d
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