Issue 34, 2016, Issue in Progress

Mycobacterium tuberculosis histidinol dehydrogenase: biochemical characterization and inhibition studies

Abstract

HisD-Encoded histidinol dehydrogenase (HisD) catalyzes the two last chemical reactions of the L-histidine biosynthetic pathway, namely the conversion of L-histidinol (L-Hol) to L-histidinaldehyde (L-Hal) and to L-histidine (L-His). The hisD gene product has been shown to be essential for Mycobacterium tuberculosis survival in vitro. Herein, we describe a series of biochemical studies on recombinant Mycobacterium tuberculosis HisD (MtHisD). The synthesis of hydrazones derived from L-histidine yielded inhibitors in the low micromolar range, one of which showed moderate anti-Mtb activity. The compounds described here are, to the best of our knowledge, the first inhibitors of MtHisD activity reported in the literature, and they could become promising candidates for future development.

Graphical abstract: Mycobacterium tuberculosis histidinol dehydrogenase: biochemical characterization and inhibition studies

Supplementary files

Article information

Article type
Paper
Submitted
01 Feb 2016
Accepted
10 Mar 2016
First published
11 Mar 2016

RSC Adv., 2016,6, 28406-28418

Mycobacterium tuberculosis histidinol dehydrogenase: biochemical characterization and inhibition studies

J. Lunardi, L. K. Borges Martinelli, A. S. Raupp, J. E. Sacconi Nunes, D. C. Rostirolla, L. F. Saraiva Macedo Timmers, A. D. Villela, K. Pissinate, J. Limberger, O. Norberto de Souza, L. A. Basso, D. S. Santos and P. Machado, RSC Adv., 2016, 6, 28406 DOI: 10.1039/C6RA03020C

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