Journal article

1,3-Phenylene bis(ketoacid) derivatives as inhibitors of Escherichia coli dihydrodipicolinate synthase

BA Boughton, L Hor, JA Gerrard, CA Hutton

Bioorganic and Medicinal Chemistry | Published : 2012

Abstract

Dihydrodipicolinate synthase is a key enzyme in the lysine biosynthesis pathway that catalyzes the condensation of pyruvate and aspartate semi-aldehyde. A series of phenolic ketoacid derivatives that mimic the proposed enzymatic intermediate were designed as potential inhibitors of this enzyme and were synthesized from simple precursors. The ketoacid derivatives were shown to act as slow and slow-tight binding inhibitors. Mass spectrometric experiments provided further evidence to support the proposed model of inhibition, demonstrating either an encounter complex or a condensation product for the slow and slow-tight binding inhibitors, respectively. © 2012 Elsevier Ltd. All rights reserved.

University of Melbourne Researchers

Grants

Awarded by Defense Threat Reduction Agency


Funding Acknowledgements

This work was supported by the Defense Threat Reduction Agency (Project ID AB07CBT004) (C. A. H.) and the Royal Society of New Zealand Marsden Fund (J.A.G. and C.A.H.). The authors thank R.C.J. Dobson, S.R.A. Devenish, F.G. Pearce, S. Dommaraju and M.A. Perugini for providing samples of DHDPS and DHDPR used in enzyme assays, and for useful discussions.