School of Biological Sciences, University of Bristol, Bristol, United Kingdom.
Department of Chemistry, University of Warwick, Coventry, United Kingdom.
PLoS One. 2020 Apr 6;15(4):e0229925. doi: 10.1371/journal.pone.0229925. eCollection 2020.
Basidiomycete fungi are a rich source of natural products with a diverse array of potentially exploitable bioactivities. Two dimeric sesquiterpenes, bovistol B (1) and D (2), and one monomeric sesquiterpene, strossmayerin (7), were isolated from the culture filtrate of the basidiomycete fungus Coprinopsis strossmayeri. The structures were determined through a combination of MS and 1D/2D NMR spectroscopic techniques. Likely monomeric precursors, identified on the basis of HRMS analysis, allow a plausible biosynthetic pathway to be proposed for the biosynthesis of 1 and 2, involving the dimerisation of the monomer through a hetero-Diels-Alder mechanism. A gene cluster, including a putative sesquiterpene 1-11 cyclase, was identified through phylogenetic and RNA-seq analysis, and is proposed to be responsible for the biosynthesis of 1 and 2.
担子菌真菌是天然产物的丰富来源,具有多种多样潜在可开发的生物活性。从担子菌Coprinopsis strossmayeri 的培养滤液中分离得到两种二聚倍半萜类化合物 bovistol B(1)和 D(2),以及一种单体倍半萜类化合物 strossmayerin(7)。通过 MS 和 1D/2D NMR 波谱技术的组合确定了它们的结构。根据高分辨质谱分析确定的可能的单体前体,提出了 1 和 2 的生物合成途径,涉及通过杂 Diels-Alder 机制将单体二聚化。通过系统发育和 RNA-seq 分析鉴定了一个包括一个假定的倍半萜 1-11 环化酶的基因簇,该基因簇被认为负责 1 和 2 的生物合成。