| Literature DB >> 29797385 |
Xuan Zhang1, Ting Ting Wang1, Qin Lan Xu1, Ying Xiong1, Li Zhang1, Hao Han1, Kuang Xu1, Wen Jie Guo1, Qiang Xu1, Ren Xiang Tan1,2, Hui Ming Ge1.
Abstract
Two homologous meroterpenoid gene clusters consisting of contiguous genes encoding polyketide synthase (PKS), prenyltransferase (PT), terpenoid cyclase (TC) and other tailoring enzymes were identified from two phylogenetically distinct fungi through computational analysis. Media optimization guided by reverse-transcription PCR (RT-PCR) enabled two strains to produce eight new and two known meroterpenoids (1-10). Using gene inactivation, heterologous expression, and biochemical analyses, we revealed a new polyketide-terpenoid assembly line that utilizes a pair of PKSs to synthesize 2,4-dihydroxy-6-alkylbenzoic acid, followed by oxidative decarboxylation, farnesyl transfer, and terpene cyclization to construct the meroterpenoid scaffold. In addition, two of the isolated meroterpenoids (3 and 17 d) showed immunosuppressive bioactivity. Our work reveals a new strategy for meroterpenoid natural products discovery, and reveals the biosynthetic pathway for compounds 1-10.Entities:
Keywords: biosynthesis; genome mining; immunosuppressants; meroterpenoids; natural products
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Year: 2018 PMID: 29797385 DOI: 10.1002/anie.201804317
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336