Elucidation of the Verrucofortine Biosynthetic Pathway Enables Identification of a Cyclodipeptide Prenyltransferase with High Catalytic Efficiency

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Authors: Hui-Ling Wei, Li-Dan Pang, Xiaoling Chen, Shu‐Ming Li
Cited by: 0
References: 41

Abstract

High Resolution Image Download MS PowerPoint Slide Penicillium polonicum, a common spoilage fungus affecting stored grains, nuts, and dried fruits, produces diverse secondary metabolites, including the indole-diketopiperazine derivative verrucofortine. Here, we elucidate its biosynthetic pathway through targeted gene deletion in a constructed low-metabolite-background strain and biochemical characterization with recombinant proteins. A nonribosomal peptide synthetase (VftPS) is responsible for assembling the cyclodipeptide scaffold, which is then modified by the prenyltransferase VftPT and the acetyltransferase VftAT. Notably, VftPT shows higher catalytic efficiency toward all the tested tryptophan-containing cyclodipeptides for C3ß -prenylation at the indole ring than its known homologues, highlighting its potential for biocatalysis and small molecule modification.

Fields of Study & Subjects

Microbial Natural Products and Biosynthesis Microbial Metabolism and Applications Mycotoxins in Agriculture and Food

Publication details

Journal / source
Journal of Agricultural and Food Chemistry
Volume
74
Issue
9
Pages
7752–7762
Publication date
3 March 2026
Language
EN