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J Nat Prod ; 86(2): 398-405, 2023 02 24.
Article in English | MEDLINE | ID: mdl-36762727

ABSTRACT

By mining fungal genomic information, a noncanonical iterative type I PKS fused with an N-terminal adenylation-thiolation didomain, which catalyzes the formation of naringenin chalcone, was found. Structural prediction and molecular docking analysis indicated that a C-terminal thioesterase domain was involved in the Claisen-type cyclization. An enzyme responsible for formation of (2S)-flavanone in the biosynthesis of fungal flavonoids was also identified. Collectively, these findings demonstrate unprecedented fungal biosynthetic machinery leading to plant-like metabolites.


Subject(s)
Acyltransferases , Flavonoids , Molecular Docking Simulation , Flavonoids/chemistry
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