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Publication Abstract from PubMed

Prenylation of amino acids is a critical step for synthesizing building blocks of prenylated alkaloid family natural products, where the corresponding prenyltransferase that catalyzes prenylation on free l-histidine (l-His) has not yet been identified. Here, we first discovered and characterized a prenyltransferase FunA from the antifungal agent fungerin pathway that efficiently performs C4-dimethylallylation on l-His. Crystal structure-guided engineering of the prenyl-binding pocket of FunA, a single M181A mutation, successfully converted it into a C4-geranyltransferase. Furthermore, FunA and its variant FunA-M181A show broad substrate promiscuity toward substrates that vary in substituents of the imidazole ring. Our work furthers our knowledge of free amino acid prenyltransferase and expands the arsenal of alkylation biocatalysts for imidazole-containing small molecules.

Discovery, Characterization and Engineering of the Free l-Histidine C4-Prenyltransferase.,Chen XW, Liu Z, Dai S, Zou Y J Am Chem Soc. 2024 Aug 28;146(34):23686-23691. doi: 10.1021/jacs.4c08388. Epub , 2024 Aug 14. PMID:39140691^[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.