Issue 13, 1984

Stereochemical studies of processing of D- and L-isomers of suicide substrates by an amino acid racemase from Pseudomonas striata

Abstract

Modest stereoselectivity (15–20% enantiomeric excess) is observed in the protonation of the aminoacrylate product that forms in kinetic competition with suicidal capture of the pyridoxal phosphate (PLP) cofactor by that aminoacrylate in the inactivation of a racemase (Pseudomonas striata) with O-acetylserines.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 838-840

Stereochemical studies of processing of D- and L-isomers of suicide substrates by an amino acid racemase from Pseudomonas striata

B. Badet, K. Lee, H. G. Floss and C. T. Walsh, J. Chem. Soc., Chem. Commun., 1984, 838 DOI: 10.1039/C39840000838

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