Mycobacterium tuberculosis histidinol dehydrogenase: biochemical characterization and inhibition studies

被引:4
作者
Lunardi, Juleane [1 ,2 ,3 ]
Borges Martinelli, Leonardo Kras [1 ]
Raupp, Alessandra Silva [1 ]
Sacconi Nunes, Jose Eduardo [3 ]
Rostirolla, Diana Carolina [1 ]
Saraiva Macedo Timmers, Luis Fernando [4 ]
Villela, Anne Drumond [1 ]
Pissinate, Kenia [1 ]
Limberger, Jones [1 ]
de Souza, Osmar Norberto [1 ,2 ,4 ]
Basso, Luiz Augusto [1 ,2 ,3 ]
Santos, Diogenes Santiago [1 ,2 ,3 ]
Machado, Pablo [1 ,2 ]
机构
[1] Pontificia Univ Catolica Rio Grande do Sul, Ctr Pesquisas Biol Mol & Func, INCT TB, BR-90619900 Porto Alegre, RS, Brazil
[2] Pontificia Univ Catolica Rio Grande do Sul, Programa Posgrad Biol Celular & Mol, BR-90619900 Porto Alegre, RS, Brazil
[3] Quatro G Pesquisa & Desenvolvimento Ltda, BR-90619900 Porto Alegre, RS, Brazil
[4] Pontificia Univ Catolica Rio Grande do Sul, Lab Bioinformat Modelagem & Simulacao Biossistema, BR-90619900 Porto Alegre, RS, Brazil
关键词
SALMONELLA-TYPHIMURIUM; BIOSYNTHESIS; MACROPHAGE; MECHANISM; PATHWAY; BINDING;
D O I
10.1039/c6ra03020c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:28406 / 28418
页数:13
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