Ruggieri S, Lauro L, Vincenzetti S, Santarelli I, Balducci E, Vita A, Magni G, Natalini P
Department of Cell Biology, University of Camerino, Italy.
Experientia. 1991 Jun 15;47(6):610-2. doi: 10.1007/BF01949886.
NAD pyrophosphorylase (ATP:NMN adenylyltransferase) activity has been measured in the skeletal muscle of dystrophic mice. The amount of this enzyme in the dystrophic mice, as determined by three different methods, was about one half of that in the controls. In addition, the concentration of ATP was too low to be detected in crude extracts of dystrophic mouse skeletal muscle, which were prepared using Tris buffer alone or Tris buffer containing either 3 M KCl, or 1 mM PMSF.
已对营养不良小鼠骨骼肌中的NAD焦磷酸化酶(ATP:NMN腺苷酸转移酶)活性进行了测定。通过三种不同方法测定,营养不良小鼠体内这种酶的量约为对照组的一半。此外,在仅使用Tris缓冲液或含有3 M KCl或1 mM PMSF的Tris缓冲液制备的营养不良小鼠骨骼肌粗提物中,ATP浓度过低无法检测到。