Brzozowski T H, Kalman S M
J Bacteriol. 1966 Jun;91(6):2286-90. doi: 10.1128/jb.91.6.2286-2290.1966.
Brzozowski, Thomas H. (Stanford University School of Medicine, Palo Alto, Calif.), and Sumner M. Kalman. Carbamyl phosphate and acetyl phosphate synthesis in Escherichia coli: analysis of associated enzyme activities by an antibody to acetokinase. J. Bacteriol. 91:2286-2290. 1966.-Earlier studies have shown that the carbamyl phosphate synthesis from ammonia in cell extracts of wild-type Escherichia coli is due to at least two enzymes, acetokinase and the glutamine-dependent carbamyl phosphate synthetase. Partial purification of the glutamine-dependent carbamyl phosphate synthetase and acetokinase fails to separate from these enzymes this ammonia-dependent activity. An antibody to the partially purified acetokinase was prepared and used to determine the distribution of the ammonia-dependent activity in wild-type organisms and single-step arginine-uracil-requiring mutants with respect to the two enzymes. Such a study was possible because the antibody inhibits acetokinase but not the glutamine-utilizing carbamyl phosphate synthetase. Enzyme inhibition obtained by the stepwise addition of the antibody to cell extracts indicates that all of the ammonia-dependent carbamyl phosphate synthesis observed in the arginine-uracil-requiring mutants is due to a protein in the acetokinase fraction, presumably acetokinase itself, since acetyl phosphate and carbamyl phosphate synthesis were inhibited in a parallel fashion. In wild-type organisms, there is only partial inhibition of the ammonia-dependent activity, even when enough antibody is added to produce maximal inhibition of acetokinase. It is suggested that this residue is due to the glutamine-dependent carbamyl phosphate synthetase, for the ratio of the antibody insensitive to antibody sensitive ammonia-dependent activity present in cell extracts of the two wild-type organisms reported is qualitatively proportional to the level of carbamyl phosphate synthetase present relative to acetokinase.
布佐夫斯基,托马斯·H.(加利福尼亚州帕洛阿尔托斯坦福大学医学院),以及萨姆纳·M.卡尔曼。大肠杆菌中氨甲酰磷酸和乙酰磷酸的合成:用抗乙酰激酶抗体分析相关酶活性。《细菌学杂志》91:2286 - 2290。1966年。——早期研究表明,野生型大肠杆菌细胞提取物中由氨合成氨甲酰磷酸至少归因于两种酶,即乙酰激酶和谷氨酰胺依赖性氨甲酰磷酸合成酶。对谷氨酰胺依赖性氨甲酰磷酸合成酶和乙酰激酶进行部分纯化时,未能将这种氨依赖性活性与这些酶分离。制备了针对部分纯化的乙酰激酶的抗体,并用于确定野生型生物体和一步法需要精氨酸 - 尿嘧啶的突变体中氨依赖性活性相对于这两种酶的分布。这样的研究是可行的,因为该抗体抑制乙酰激酶,但不抑制利用谷氨酰胺的氨甲酰磷酸合成酶。通过向细胞提取物中逐步添加抗体获得的酶抑制表明,在需要精氨酸 - 尿嘧啶的突变体中观察到的所有氨依赖性氨甲酰磷酸合成均归因于乙酰激酶组分中的一种蛋白质,大概是乙酰激酶本身,因为乙酰磷酸和氨甲酰磷酸的合成以平行方式受到抑制。在野生型生物体中,即使加入足够的抗体以产生对乙酰激酶的最大抑制,氨依赖性活性也只是部分受到抑制。有人认为这种残留是由于谷氨酰胺依赖性氨甲酰磷酸合成酶所致,因为所报道的两种野生型生物体的细胞提取物中对抗体不敏感的氨依赖性活性与对抗体敏感的氨依赖性活性的比率在质量上与相对于乙酰激酶存在的氨甲酰磷酸合成酶水平成比例。