Anderson B M, Anderson C D, Van Tassell R L, Lyerly D M, Wilkins T D
Department of Biochemistry & Nutrition, Virginia Polytechnic Institute & State University, Blacksburg 24061-0308.
Arch Biochem Biophys. 1993 Jan;300(1):483-8. doi: 10.1006/abbi.1993.1065.
Recombinant Clostridium difficile glutamate dehydrogenase (L-glutamate:NAD oxidoreductase, EC 1.4.1.2) was purified 177-fold to electrophoretic homogeneity with a 62% recovery through a four-step procedure involving gel filtration and ion-exchange and dye affinity chromatography. The approximate molecular weights of the native enzyme by gel filtration and subunits by sodium dodecyl sulfate-polyacrylamide gel electrophoresis were consistent with a hexameric structure for the purified enzyme. The enzyme-catalyzed glutamate oxidation was an NAD-dependent sequential process in which NADP could not be substituted as coenzyme. Several dinucleotide analogs of NAD structurally altered in either the pyridine or the purine moiety were observed to function as coenzymes when substituted for NAD. Nicotinamide mononucleotide did not serve as a coenzyme for glutamate oxidation. Product inhibition by NADH was competitive with respect to NAD. In deadend inhibition studies, adenosine diphosphoribose was shown to be an effective coenzyme-competitive inhibitor.
重组艰难梭菌谷氨酸脱氢酶(L-谷氨酸:NAD氧化还原酶,EC 1.4.1.2)通过涉及凝胶过滤、离子交换和染料亲和色谱的四步程序纯化了177倍,回收率为62%,达到电泳纯。通过凝胶过滤测定的天然酶的近似分子量以及通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳测定的亚基分子量与纯化酶的六聚体结构一致。酶催化的谷氨酸氧化是一个依赖NAD的顺序过程,其中NADP不能作为辅酶替代。观察到几种在吡啶或嘌呤部分结构改变的NAD二核苷酸类似物在替代NAD时可作为辅酶发挥作用。烟酰胺单核苷酸不能作为谷氨酸氧化的辅酶。NADH的产物抑制相对于NAD具有竞争性。在终产物抑制研究中,腺苷二磷酸核糖被证明是一种有效的辅酶竞争性抑制剂。