Stereochemical course of the decarboxylation of (S)-glutamic acid by glutamate decarboxylase from Escherichia coli(E.C. 4.1.1.15)
- 1 January 1979
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- Vol. 7 (7), 1677-1679
- https://doi.org/10.1039/p19790001677
Abstract
Decarboxylation of (S)-glutamic acid (1) in 2H2O, catalysed by glutamate decarboxylase from Escherichia coli E.C.4.1.1.15), afforded 4-[4-2H]aminobutyric acid (2b). (+)-(S)-4-[4-2H]aminobutyric acid (2c) was synthesized and the 1H n.m.r. spectrum of the (1S,4R)-O-camphanoylamide of its methyl ester compared with the same derivative of (2b) in the presence of the shift reagent [Eu(dpm)3]. It was shown that (2b) is in the (R) configuration and that glutamate decarboxylase catalyses the decarboxylation of (1) with retention of configuration.This publication has 1 reference indexed in Scilit:
- Stereochemistry of reactions catalyzed by glutamate decarboxylaseBiochemistry, 1978