| Literature DB >> 26437744 |
Jutta Siegrist1, Simon Aschwanden2, Silja Mordhorst1, Linda Thöny-Meyer2,3, Michael Richter4,5, Jennifer N Andexer6.
Abstract
S-Adenosylmethionine (SAM)-dependent enzymes have great potential for selective alkylation processes. In this study we investigated the regiocomplementary O-methylation of catechols. Enzymatic methylation is often hampered by the need for a stoichiometric supply of SAM and the inhibitory effect of the SAM-derived byproduct on most methyltransferases. To counteract these issues we set up an enzyme cascade. Firstly, SAM was generated from l-methionine and ATP by use of an archaeal methionine adenosyltransferase. Secondly, 4-O-methylation of the substrates dopamine and dihydrocaffeic acid was achieved by use of SafC from the saframycin biosynthesis pathway in 40-70 % yield and high selectivity. The regiocomplementary 3-O-methylation was catalysed by catechol O-methyltransferase from rat. Thirdly, the beneficial influence of a nucleosidase on the overall conversion was demonstrated. The results of this study are important milestones on the pathway to catalytic SAM-dependent alkylation processes.Entities:
Keywords: S-adenosylmethionine; biotransformations; cofactors; methyltransferases; multi-enzyme reactions
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Year: 2015 PMID: 26437744 DOI: 10.1002/cbic.201500410
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164