Abstract
The sequence motif commonly called a Nudix box, represented by (GX5EX7REVXEEXGU) is the marker of a widely distributed family of enzymes that catalyze the hydrolysis of a variety of nucleoside diphosphate derivatives. Here we describe the cloning and characterization of an Arabidopsis thaliana cDNA encoding a Nudix hydrolase that degrades NADH. The deduced amino acid sequence of AtNUDT1 contains 147 amino acids. The recombinant AtNUDT1 was expressed in Escherichia coli and purified. In the presence of Mn2+ and the optimal pH of 7. 0, the recombinant AtNUDT1 catalyzed the hydrolysis of NADH with a Km value of 0. 36 mM. A Vmax of 12. 7 units mg -1 for NADH was determined. The recombinant AtNUDT1 migrated as a dimer on a gel filtration column. Biochemical analysis of recombinant AtNUDT1 indicated that the first characterized member of the Nudix family from A. thaliana is a NADH pyrophosphatase.
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CITATION STYLE
Dobrzanska, M., Szurmak, B., Wyslouch-Cieszynska, A., & Kraszewska, E. (2002). Cloning and characterization of the first member of the Nudix family from Arabidopsis thaliana. Journal of Biological Chemistry, 277(52), 50482–50486. https://doi.org/10.1074/jbc.M205207200
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