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.
Authors
- Xiao-Xin Xue
- Xu‐Dong Kong (ORCID: https://orcid.org/0000-0003-3216-7545)
- Man‐Cheng Tang (ORCID: https://orcid.org/0000-0001-9418-3239)
- Meng-Jie Zhang (ORCID: https://orcid.org/0009-0008-4604-7222)
- Lin Chen
Institutions
- Shanghai Jiao Tong University (CN)
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
Funders
- Shanghai City Youth Science and Technology Star Project
- National Key Research and Development Program of China