Methyltransferase Domain-Focused Genome Mining for Fungal Polyketide Synthases

A comparison of substrate-binding site amino acid residues in the C-methyltransferase (MT) domains of fungal nonreducing polyketide synthases (NR-PKSs) suggests that these residues are correlated with the methylation modes used by the PKSs. A PKS, designated as AsbPKS, with substrate-binding site residues distinct from those of other known PKSs is focused on. The characterization of AsbPKS revealed that it yields an isocoumarin derivative, anhydrosclerotinin B (1), the biosynthesis of which involves a previously unreported methylation pattern. This study demonstrates the utility of MT domain-focused genome mining for the discovery of PKSs with new functions. Genome mining is performed with a focus on the substrate-binding amino acid residues in the C-methyltransferase domains of fungal nonreducing polyketide synthases (NR-PKSs). An NR-PKS designated as AsbPKS is discovered and found to be responsible for the formation of anhydrosclerotinin B (1), the biosynthesis of which adopts a previously unreported methylation pattern. image