The flavoprotein-catalyzed reduction of aliphatic nitro-compounds represents a biocatalytic equivalent to the Nef-reaction

Literature Information

Publication Date 2010-02-08
DOI 10.1039/B922691E
Impact Factor 10.182
Authors

Katharina Durchschein, Bianca Ferreira-da Silva, Silvia Wallner, Peter Macheroux, Wolfgang Kroutil, Silvia Maria Glueck, Kurt Faber


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Abstract

The bioreduction of aliphatic sec-nitro compounds catalyzed by purified flavoproteins from the old-yellow-enzyme family unexpectedly furnished the corresponding carbonyl compounds instead of the expected amines and thus represents a biocatalytic equivalent to the Nef-reaction. The pathway was shown to proceed via initial reduction of the nitro-group to yield the nitroso-derivative, which spontaneously tautomerized to yield the more stable oxime, which was enzymatically reduced in a second step to furnish a hydrolytically unstable imine-species, which spontaneously hydrolyzed to finally give a carbonyl compound and ammonia.

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Inside back cover

Cover

DOI: 10.1039/C9CP90212K

Back cover

Cover

DOI: 10.1039/C9CP90213A

Contents list

Front/Back Matter

DOI: 10.1039/C9CP90298H

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