Kinetic and mutational studies of the adenosine diphosphate ribose hydrolase from Mycobacterium tuberculosis

Abstract

Mycobacterium tuberculosis represents one of the world's most devastating infectious agents – with one third of the world's population infected and 1.5 million people dying each year from this deadly pathogen. As part of an effort to identify targets for therapeutic intervention, we carried out the kinetic characterization of the product of gene rv1700 of M tuberculosis. Based on its sequence and its structure, the protein had been tentatively identified as a pyrophosphohydrolase specific for adenosine diphosphate ribose (ADPR), a compound involved in various pathways including oxidative stress response and tellurite resistance. In this work we carry out a kinetic, mutational and structural investigation of the enzyme, which provides a full characterization of this Mt-ADPRase. Optimal catalytic rates were achieved at alkaline pH (7.5-8.5) with either 0.5-1 mM Mg2+ or 0.02-1 mM Mn2+. Km and kcat values for hydrolysis of ADPR with Mg2+ ions are 200±19 μM and 14.4±0.4 s-1, and with Mn2+ ions are 554±64 μM and 28.9±1.4 s-1. Four residues proposed to be important in the catalytic mechanism of the enzyme were individually mutated and the kinetics of the mutant enzymes were characterized. In the four cases, the Km increased only slightly (2- to 3-fold) but the kcat decreased significantly (300- to 1900-fold), confirming the participation of these residues in catalysis. An analysis of the sequence and structure conservation patterns in Nudix ADPRases permits an unambiguous identification of members of the family and provides insight into residues involved in catalysis and their participation in substrate recognition in the Mt-ADPRase.

Visualization of mutagenic nucleotide processing by Escherichia coli MutT, a Nudix hydrolase

“…S9 ). Mutations in Glu142 in M. tuberculosis ADPRase and Glu166 in human NUDT5 considerably decrease k cat , indicating that they are involved in the deprotonation of the water molecule ( 30 , 45 ). However, mutational analysis of T. thermophilus ADPRase revealed that the mutants, Asp126, Glu127, Asp128, and Glu129, on the equivalent loop retain normal activity ( 46 ).…”