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含顺式-十氢化萘的四氢酸作为昆虫甾体生物合成谷胱甘肽 S-转移酶 Noppera-bo 的抑制剂。

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

机构信息

Natural Product Biosynthesis Research Unit, RIKEN Center for Sustainable Research Science, Wako, Saitama, Japan.

Faculty of Agriculture, Setsunan University, Hirakata, Osaka, Japan.

出版信息

PLoS One. 2023 Aug 31;18(8):e0290851. doi: 10.1371/journal.pone.0290851. eCollection 2023.

Abstract

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.

摘要

含癸烷四酸的二萜是一种生物活性支架,主要由丝状真菌产生。这组化合物的结构多样性是由真菌生物合成途径的特征酶产生的,包括聚酮合酶/非核糖体肽合酶杂合酶和癸烷合酶,它们分别负责通过分子内 Diels-Alder 反应构建线性多烯酰基四酸结构和立体选择性癸烷形成。从产生含癸烷四酸的真菌的基因工程突变体中收集了仅在癸烷构型上有所不同的化合物,并用于进行构效关系研究。我们对生物活性的评估,如对几种癌细胞系的细胞毒性以及抗菌、抗真菌、抗疟和线粒体抑制活性,表明每种测定的活性因癸烷构型而异。除了这些已知的生物活性外,我们还发现这些化合物对昆虫甾体生成谷胱甘肽 S-转移酶 Noppera-bo 具有抑制活性。对癸烷构型进行工程改造不仅有助于发现具有更好生物活性的衍生物,还可以发现被忽视的生物活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e981/10470909/a4d204761e65/pone.0290851.g001.jpg

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