Dobrzanska Marta, Szurmak Blanka, Wyslouch-Cieszynska Aleksandra, Kraszewska Elzbieta
Departament of Plant Biochemistry, Mass Spectrometry Laboratory, Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawinskiego 5A, 02-106 Warsaw, Poland.
J Biol Chem. 2002 Dec 27;277(52):50482-6. doi: 10.1074/jbc.M205207200. Epub 2002 Oct 23.
The sequence motif commonly called a Nudix box, represented by (GX(5)EX(7)REVXEEXGU) 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 Mn(2+) and the optimal pH of 7. 0, the recombinant AtNUDT1 catalyzed the hydrolysis of NADH with a K(m) value of 0. 36 mm. A V(max) 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.
通常被称为Nudix框的序列基序,由(GX(5)EX(7)REVXEEXGU)表示,是一类广泛分布的酶家族的标志,这类酶催化多种核苷二磷酸衍生物的水解。在这里,我们描述了拟南芥中一个编码降解NADH的Nudix水解酶的cDNA的克隆和特性分析。AtNUDT1推导的氨基酸序列包含147个氨基酸。重组AtNUDT1在大肠杆菌中表达并纯化。在Mn(2+)存在且最适pH为7.0的条件下,重组AtNUDT1催化NADH水解,K(m)值为0.36 mM。测定NADH的V(max)为12.7单位mg(-1)。重组AtNUDT1在凝胶过滤柱上以二聚体形式迁移。重组AtNUDT1的生化分析表明,拟南芥Nudix家族第一个被鉴定的成员是一种NADH焦磷酸酶。