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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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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. |
format | Online Article Text |
id | pubmed-8697804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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