Biosynthesis of Viridicatol in Penicillium palitans Implies a Cytochrome P450-Mediated meta Hydroxylation at a Monoalkylated Benzene Ring.

Cyclopenol ( 1 ) and viridicatol ( 6 ) with m -hydroxyl groups were isolated from a culture of Penicillium palitans . Genome mining and heterologous expression in Aspergillus nidulans led to the identification of their biosynthetic gene cluster and the cytochrome P450 enzyme VdoD responsible for the meta hydroxylation. Precursor feeding experiments into vdoD transformant proved the conversion of cyclopenin ( 2 ) to 1 , which then undergoes a spontaneous or VdoA-catalyzed rearrangement to 6 . A direct conversion of viridicatin ( 5 ) to 6 by VdoD was not detected.