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cis-Decalin-containing tetramic acids as inhibitors of insect steroidogenic glutathione S-transferase Noppera-bo

Decalin-containing tetramic acid is a bioactive scaffold primarily produced by filamentous fungi. The structural diversity of this group of compounds is generated by characteristic enzymes of fungal biosynthetic pathways, including polyketide synthase/nonribosomal peptide synthetase hybrid enzymes a...

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Autores principales: Kato, Naoki, Ebihara, Kana, Nogawa, Toshihiko, Futamura, Yushi, Inaba, Kazue, Okano, Akiko, Aono, Harumi, Fujikawa, Yuuta, Inoue, Hideshi, Matsuda, Kazuhiko, Osada, Hiroyuki, Niwa, Ryusuke, Takahashi, Shunji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470909/
https://www.ncbi.nlm.nih.gov/pubmed/37651399
http://dx.doi.org/10.1371/journal.pone.0290851
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author Kato, Naoki
Ebihara, Kana
Nogawa, Toshihiko
Futamura, Yushi
Inaba, Kazue
Okano, Akiko
Aono, Harumi
Fujikawa, Yuuta
Inoue, Hideshi
Matsuda, Kazuhiko
Osada, Hiroyuki
Niwa, Ryusuke
Takahashi, Shunji
author_facet Kato, Naoki
Ebihara, Kana
Nogawa, Toshihiko
Futamura, Yushi
Inaba, Kazue
Okano, Akiko
Aono, Harumi
Fujikawa, Yuuta
Inoue, Hideshi
Matsuda, Kazuhiko
Osada, Hiroyuki
Niwa, Ryusuke
Takahashi, Shunji
author_sort Kato, Naoki
collection PubMed
description Decalin-containing tetramic acid is a bioactive scaffold primarily produced by filamentous fungi. The structural diversity of this group of compounds is generated by characteristic enzymes of fungal biosynthetic pathways, including polyketide synthase/nonribosomal peptide synthetase hybrid enzymes and decalin synthase, which are responsible for the construction of a linear polyenoyl tetramic acid structure and stereoselective decalin formation via the intramolecular Diels–Alder reaction, respectively. Compounds that differed only in the decalin configuration were collected from genetically engineered mutants derived from decalin-containing tetramic acid-producing fungi and used for a structure-activity relationship study. Our evaluation of biological activities, such as cytotoxicity against several cancer cell lines and antibacterial, antifungal, antimalarial, and mitochondrial inhibitory activities, demonstrated that the activity for each assay varies depending on the decalin configurations. In addition to these known biological activities, we revealed that the compounds showed inhibitory activity against the insect steroidogenic glutathione S-transferase Noppera-bo. Engineering the decalin configurations would be useful not only to find derivatives with better biological activities but also to discover overlooked biological activities.
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spelling pubmed-104709092023-09-01 cis-Decalin-containing tetramic acids as inhibitors of insect steroidogenic glutathione S-transferase Noppera-bo Kato, Naoki Ebihara, Kana Nogawa, Toshihiko Futamura, Yushi Inaba, Kazue Okano, Akiko Aono, Harumi Fujikawa, Yuuta Inoue, Hideshi Matsuda, Kazuhiko Osada, Hiroyuki Niwa, Ryusuke Takahashi, Shunji PLoS One Research Article Decalin-containing tetramic acid is a bioactive scaffold primarily produced by filamentous fungi. The structural diversity of this group of compounds is generated by characteristic enzymes of fungal biosynthetic pathways, including polyketide synthase/nonribosomal peptide synthetase hybrid enzymes and decalin synthase, which are responsible for the construction of a linear polyenoyl tetramic acid structure and stereoselective decalin formation via the intramolecular Diels–Alder reaction, respectively. Compounds that differed only in the decalin configuration were collected from genetically engineered mutants derived from decalin-containing tetramic acid-producing fungi and used for a structure-activity relationship study. Our evaluation of biological activities, such as cytotoxicity against several cancer cell lines and antibacterial, antifungal, antimalarial, and mitochondrial inhibitory activities, demonstrated that the activity for each assay varies depending on the decalin configurations. In addition to these known biological activities, we revealed that the compounds showed inhibitory activity against the insect steroidogenic glutathione S-transferase Noppera-bo. Engineering the decalin configurations would be useful not only to find derivatives with better biological activities but also to discover overlooked biological activities. Public Library of Science 2023-08-31 /pmc/articles/PMC10470909/ /pubmed/37651399 http://dx.doi.org/10.1371/journal.pone.0290851 Text en © 2023 Kato et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed 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 author and source are credited.
spellingShingle Research Article
Kato, Naoki
Ebihara, Kana
Nogawa, Toshihiko
Futamura, Yushi
Inaba, Kazue
Okano, Akiko
Aono, Harumi
Fujikawa, Yuuta
Inoue, Hideshi
Matsuda, Kazuhiko
Osada, Hiroyuki
Niwa, Ryusuke
Takahashi, Shunji
cis-Decalin-containing tetramic acids as inhibitors of insect steroidogenic glutathione S-transferase Noppera-bo
title cis-Decalin-containing tetramic acids as inhibitors of insect steroidogenic glutathione S-transferase Noppera-bo
title_full cis-Decalin-containing tetramic acids as inhibitors of insect steroidogenic glutathione S-transferase Noppera-bo
title_fullStr cis-Decalin-containing tetramic acids as inhibitors of insect steroidogenic glutathione S-transferase Noppera-bo
title_full_unstemmed cis-Decalin-containing tetramic acids as inhibitors of insect steroidogenic glutathione S-transferase Noppera-bo
title_short cis-Decalin-containing tetramic acids as inhibitors of insect steroidogenic glutathione S-transferase Noppera-bo
title_sort cis-decalin-containing tetramic acids as inhibitors of insect steroidogenic glutathione s-transferase noppera-bo
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470909/
https://www.ncbi.nlm.nih.gov/pubmed/37651399
http://dx.doi.org/10.1371/journal.pone.0290851
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