Issue 18, 1987

Mechanism of the enzymic elimination of ammonia from 3-substituted aspartic acids by 3-methylaspartase

Abstract

Kinetic experiments with 3-methylaspartase, using aspartic, 3-methylaspartic, and 3-ethylaspartic acid and the appropriate C-3 deuteriated isotopomers as substrates, reveal that C(3)–H bond cleavage is partially rate-limiting for 3-methylaspartic acid, much less rate-limiting for 3-ethylaspartic acid, and not rate-limiting at all for aspartic acid.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 1371-1373

Mechanism of the enzymic elimination of ammonia from 3-substituted aspartic acids by 3-methylaspartase

N. P. Botting, M. Akhtar, M. A. Cohen and D. Gani, J. Chem. Soc., Chem. Commun., 1987, 1371 DOI: 10.1039/C39870001371

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements