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Chem Commun (Camb) ; (7): 877-9, 2005 Feb 21.
Article in English | MEDLINE | ID: mdl-15700067

ABSTRACT

The introduction of two mutations (G74C/C188S) based on the estimated reaction mechanism resulted in the inversion of enantioselectivity of arylmalonate decarboxylase, which catalyses the asymmetric decarboxylation of arylmethylmalonate to give optically active arylpropionate.


Subject(s)
Carboxy-Lyases/chemistry , Carboxy-Lyases/genetics , Methylmalonic Acid/chemistry , Propionates/chemical synthesis , Amino Acid Sequence , Catalysis , Decarboxylation , Molecular Conformation , Molecular Sequence Data , Mutagenesis, Site-Directed , Stereoisomerism
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