Harden K K, Robinson J L
Department of Animal Sciences, University of Illinois, Urbana 61801.
Biochem Genet. 1987 Aug;25(7-8):465-75. doi: 10.1007/BF00554349.
UMP synthase was characterized biochemically in dairy cattle heterozygous for a deficiency of this enzyme. Both activities comprising this bifunctional enzyme are decreased, with OMP decarboxylase more affected than orotate phosphoribosyltransferase. Immunotitration of UMP synthase activity revealed the presence of the protein product of the mutant allele in the heterozygous animals. UMP synthases from normal and deficient cattle were not distinguished from one another by kinetic constants, responses to inhibitors, pH profiles, or thermal lability. It was concluded that the 50% reduction in enzyme activity in heterozygous cattle is the result of the presence of only half the normal level of catalytically active UMP synthase.
在患有该酶缺乏症的杂合奶牛中对尿苷一磷酸合酶进行了生化特性分析。构成这种双功能酶的两种活性均降低,其中乳清酸脱羧酶比乳清酸磷酸核糖基转移酶受影响更大。对尿苷一磷酸合酶活性的免疫滴定显示,杂合动物中存在突变等位基因的蛋白质产物。正常和缺陷奶牛的尿苷一磷酸合酶在动力学常数、对抑制剂的反应、pH曲线或热稳定性方面没有区别。得出的结论是,杂合奶牛中酶活性降低50%是由于催化活性尿苷一磷酸合酶的水平仅为正常水平的一半。