Dihydrobenzofuran Formation through Ring Contraction of Dihydroisocoumarin Synthesized by a Polyketide Synthase Assembly Line with a Terminal Reductase Domain in Asperfuran Biosynthesis

Abstract Asperfuran is an antifungal natural product with a dihydrobenzofuran (DHB) nucleus. Herein, we identify a biosynthetic gene cluster responsible for its biosynthesis from Neosartorya pseudofischeri. Genetic and biochemical analysis revealed that the DHB nucleus of asperfuran is formed by a flavin-dependent monooxygenase-catalyzed ring contraction of a dihydroisocoumarin precursor, which is generated by a collaborative polyketide synthase assembly line with a C-terminal reductase domain. Our work unraveled a novel biosynthetic route to DHB synthesis.

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Publication Details

Journal
Organic Letters
Published
2026-09-12
DOI
https://doi.org/10.1021/acs.orglett.6c03619
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Dihydrobenzofuran Formation through Ring Contraction of Dihydroisocoumarin Synthesized by a Polyketide Synthase Assembly Line with a Terminal Reductase Domain in Asperfuran Biosynthesis

Xiao-Xin Xue, Xu‐Dong Kong, Man‐Cheng Tang, Meng-Jie Zhang et al.
Organic Letters
Microbial Natural Products and Biosynthesis
article

Dihydrobenzofuran Formation through Ring Contraction of Dihydroisocoumarin Synthesized by a Polyketide Synthase Assembly Line with a Terminal Reductase Domain in Asperfuran Biosynthesis

Xiao-Xin Xue, Xu‐Dong Kong, Man‐Cheng Tang, Meng-Jie Zhang, Lin Chen
article en

Abstract

Abstract Asperfuran is an antifungal natural product with a dihydrobenzofuran (DHB) nucleus. Herein, we identify a biosynthetic gene cluster responsible for its biosynthesis from Neosartorya pseudofischeri. Genetic and biochemical analysis revealed that the DHB nucleus of asperfuran is formed by a flavin-dependent monooxygenase-catalyzed ring contraction of a dihydroisocoumarin precursor, which is generated by a collaborative polyketide synthase assembly line with a C-terminal reductase domain. Our work unraveled a novel biosynthetic route to DHB synthesis.

Organic Letters
Shanghai Jiao Tong University (CN)
Shanghai City Youth Science and Technology Star Project, National Key Research and Development Program of China
Openalex Percentile: Top 12%
Microbial Natural Products and Biosynthesis
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Dihydrobenzofuran Formation through Ring Contraction of Dihydroisocoumarin Synthesized by a Polyketide Synthase Assembly Line with a Terminal Reductase Domain in Asperfuran Biosynthesis — Xiao-Xin Xue, Xu‐Dong Kong, et al. · Organic Letters (2026) | TGRS Research Map | TGRS