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Recent advances in methyltransferase biocatalysis. | LitMetric

Recent advances in methyltransferase biocatalysis.

Curr Opin Chem Biol

School of Chemistry & Manchester Institute of Biotechnology, University of Manchester, 131 Princess Street, Manchester M1 7DN, United Kingdom. Electronic address:

Published: April 2017

AI Article Synopsis

  • S-adenosyl-L-methionine (SAM)-dependent methyltransferases are key enzymes that methylate various small molecules and biopolymers, with recent advancements focused on their synthetic applications.
  • Research highlights the use of SAM analogs and metabolic engineering to boost SAM production and explore more stable and efficient methyltransferase variants for diverse reactions.
  • The review also discusses improving enzyme selectivity through mutagenesis and potential applications in multi-enzyme reactions, while addressing future research challenges in the field.

Article Abstract

S-adenosyl-L-methionine-dependent methyltransferses are ubiquitous in nature, methylating a vast range of small molecule metabolites, as well as biopolymers. This review covers the recent advances in the development of methyltransferase enzymes for synthetic applications, focusing on the methyltransferase catalyzed transformations with S-adenosyl methionine analogs, as well as non-native substrates. We discuss how metabolic engineering approaches have been used to enhance S-adenosyl methionine production in vivo. Enzymatic approaches that enable the more efficient generation of S-adenosyl methionine analogs, including more stable analogs, will also be described; this has expanded the biocatalytic repertoire of methyltransferases from methylation to a broader range of alkylation reactions. The review also examines how the selectivity of the methyltransferase enzymes can be improved through structure guided mutagenesis approaches. Finally, we will discuss how methyltransferases can be deployed in multi-enzyme cascade reactions and suggest future challenges and avenues for further investigation.

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Source
http://dx.doi.org/10.1016/j.cbpa.2017.01.020DOI Listing

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