Steady-state kinetics of indole-3-glycerol phosphate synthase from Mycobacterium tuberculosis |
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Authors: | Clarissa M Czekster Brenno AD Neto Jairton Dupont Luiz A Basso |
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Institution: | a Centro de Pesquisas em Biologia Molecular e Funcional, Instituto de Ciência e Tecnologia em Tuberculose, Pontifícia Universidade Católica do Rio Grande do Sul, 6681/92A Ipiranga Av., 90619-900 Porto Alegre, RS, Brazil b Programa de Pós-graduação em Ciências Biológicas: Bioquímica, Instituto de Ciências Básicas da Saúde, UFRGS, Porto Alegre, RS, Brazil c Laboratory of Molecular Catalysis - Institute of Chemistry, UFRGS, Porto Alegre, RS, Brazil |
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Abstract: | Indole-3-glycerol phosphate synthase (IGPS) catalyzes the irreversible ring closure of 1-(o-carboxyphenylamino)-1-deoxyribulose 5-phosphate (CdRP), through decarboxylation and dehydration steps, releasing indole-3-glycerol phosphate (IGP), the fourth step in the biosynthesis of tryptophan. This pathway is essential for Mycobacterium tuberculosis virulence. Here we describe the cloning, expression, purification, and kinetic characterization of IGPS from M. tuberculosis. To perform kinetic studies, CdRP was chemically synthesized, purified, and spectroscopically and spectrometrically characterized. CdRP fluorescence was pH-dependent, probably owing to excited-state intramolecular proton transfer. The activation energy was calculated, and solvent isotope effects and proton inventory studies were performed. pH-rate profiles were carried out to probe for acid/base catalysis, showing that a deprotonated residue is necessary for CdRP binding and conversion to IGP. A model to describe a steady-state kinetic sequence for MtIGPS-catalized chemical reaction is proposed. |
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Keywords: | Tuberculosis Drug target Indole-3-glycerol phosphate synthase 1-(o-Carboxyphenylamino)-1-deoxyribulose 5-phosphate IGPS Steady-state kinetics |
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