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Development of anR-Selective Amine Oxidase with Broad Substrate Specificity and High Enantioselectivity

Authors :
Marta Pontini
Beatrice Bechi
Nicholas J. Turner
Rachel S. Heath
Source :
ChemCatChem
Publication Year :
2014
Publisher :
Wiley, 2014.

Abstract

Amine oxidases are useful bio-catalysts for the synthesis of enantiomerically pure 1°, 2° and 3° chiral amines. Enzymes in this class (e.g., MAO-N from Aspergillus niger) reported previously have been shown to be highly S selective. Herein we report the development of an enantiocomplementary R-selective amine oxidase based on 6-hydroxy-D-nicotine oxidase (6-HDNO) with broadened substrate scope and high enantioselectivity. The engineered 6-HDNO enzyme has been applied to the preparative deracemisation of a range of racemic amines to yield S-configured products, for example, (S)-nicotine, in high ee.

Details

ISSN :
18673880
Volume :
6
Database :
OpenAIRE
Journal :
ChemCatChem
Accession number :
edsair.doi.dedup.....6701ead96d084325daf5e052053aec1f