Chemoselective S-adenosyl-l-methionine (SAM)-dependent methyltransferases (MTs) are a promising alternative to traditional synthetic methylation reactions. In presence of multiple nucleophiles, the enzymatic transfer of the carbon fragment is highly chemoselective for N- and O-MTs. Besides methylation, the generation of SAM derivatives enables the transfer of altered groups onto the substrates increasing the pool of products.
Abstract
Methylation reactions are of significant interest when generating pharmaceutically active molecules and building blocks for other applications. Synthetic methylating reagents are often toxic and unselective due to their high reactivity. S-Adenosyl-l-methionine (SAM)-dependent methyltransferases (MTs) present a chemoselective and environmentally friendly alternative. The anthranilate N-MT from Ruta graveolens (RgANMT) is involved in acridone alkaloid biosynthesis, methylating anthranilate. Although it is known to methylate substrates only at the N-position, the closest relatives with respect to amino acid sequence similarities of over 60 % are O-MTs catalysing the methylation reaction of caffeate and derivatives containing only hydroxyl groups (CaOMTs). In this study, we investigated the substrate range of RgANMT and a CaOMT from Prunus persica (PpCaOMT) using compounds with both, an amino- and hydroxyl group (aminophenols) as possible methyl group acceptors. For both enzymes, the reaction was highly chemoselective. Furthermore, generating cofactor derivatives in situ enabled the transfer of other alkyl chains onto the aminophenols, leading to an enlarged pool of products. Selected MT reactions were performed at a preparative biocatalytic scale in in vitro and in vivo experiments resulting in yields of up to 62 %.
