Issue 24, 2000

Remarkable enhancement of the hydrolyses of phosphoesters by dinuclear centers: Streptomyces aminopeptidase as a ‘natural model system’Electronic supplementary information (ESI) available: Michaelis–Menten kinetics plots. See http://www.rsc.org/suppdata/cc/b0/b004544f/

Abstract

The transition-state analogues bis(p-nitrophenyl)phosphate and p-nitrophenyl phenylphosphonate for peptide hydrolysis are shown to be very effectively hydrolyzed by Streptomyces dinuclear aminopeptidase and its Co2+, Ni2+, Mn2+ and Cd2+ derivatives with high catalytic proficiencies and specific activities comparable to those of some phosphoesterases.

Supplementary files

Article information

Article type
Communication
Submitted
02 Jun 2000
Accepted
27 Oct 2000
First published
29 Nov 2000

Chem. Commun., 2000, 2501-2502

Remarkable enhancement of the hydrolyses of phosphoesters by dinuclear centers: Streptomyces aminopeptidase as a ‘natural model system’

A. Ercan, H. I. Park and L. Ming, Chem. Commun., 2000, 2501 DOI: 10.1039/B004544F

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