1. Biocatalytic methylation and demethylation via a shuttle catalysis concept involving corrinoid proteins
- Author
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Wolfgang Skibar, Ferdinand Zepeck, Katharina Hiebler, Judith E. Farnberger, Mathias Pickl, Sarah Bierbaumer, Wolfgang Kroutil, and Nina Richter
- Subjects
Methyltransferase ,Chemistry ,Regioselectivity ,General Chemistry ,Methylation ,Biochemistry ,Combinatorial chemistry ,lcsh:Chemistry ,chemistry.chemical_compound ,Corrinoid ,lcsh:QD1-999 ,Biocatalysis ,Materials Chemistry ,Environmental Chemistry ,Anaerobic bacteria ,Demethylation ,Methyl group - Abstract
Synthetically established methods for methylation of phenols and demethylation of methyl phenyl ethers rely in general on hazardous reagents or/and harsh reaction conditions and are irreversible. Consequently, alternative regioselective methods for the reversible formation and breakage of C-O-ether bonds to be performed under mild and sustainable conditions are highly desired. Here we present a biocatalytic shuttle concept making use of corrinoid-dependent methyl transferases from anaerobic bacteria. The two-component enzymatic system consists of a corrinoid protein carrying the cofactor and acting as methyl group shuttle, and a methyltransferase catalyzing both methylation and demethylation in a reversible fashion. Various phenyl methyl ethers are successfully demethylated and serve in addition as sustainable methylating agents for the functionalization of various substituted catechols. Therefore, this methyl transfer approach represents a promising alternative to common chemical protocols and a valuable add-on for the toolbox of available biocatalysts. Regioselective methods for the reversible formation and breakage of C-O-ether bonds under mild conditions are desired. Here, the authors present a biocatalytic shuttle concept using corrinoid-dependent methyl transferases for demethylating various phenyl methyl ethers and functionalizing substituted catechols.
- Published
- 2018
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