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Carbamyl Phosphate and Acetyl Phosphate Synthesis in Escherichia coli: Analysis of Associated Enzyme Activities by an Antibody to Acetokinase

机译:大肠杆菌中的磷酸氨基甲酸酯和乙酰磷酸酯的合成:乙酰激酶抗体相关酶活性的分析

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摘要

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.
机译:Brzozowski,Thomas H.(加利福尼亚州帕洛阿尔托的斯坦福大学医学院)和Sumner M. Kalman。大肠杆菌中的磷酸氨基甲酸酯和乙酰基磷酸酯合成:通过抗乙酰激酶的抗体分析相关的酶活性。 J.细菌。 > 91: 2286–2290。 1966年。较早的研究表明,野生型大肠杆菌细胞提取物中从氨中合成氨基甲酸酯磷酸是由于至少两种酶,即乙酰激酶和谷氨酰胺依赖性氨基甲酸酯磷酸合成酶。谷氨酰胺依赖性氨基甲酸酯磷酸合成酶和乙酰激酶的部分纯化不能从这些酶中分离出这种氨依赖性活性。制备了针对部分纯化的乙酰激酶的抗体,并将其用于确定野生型生物体和需要单步精氨酸-尿嘧啶的突变体相对于这两种酶的氨依赖性活性的分布。这样的研究是可能的,因为该抗体抑制乙酰激酶,但不抑制利用谷氨酰胺的氨基甲酸酯磷酸合成酶。通过将抗体逐步添加到细胞提取物中获得的酶抑制作用表明,在需要精氨酸-尿嘧啶的突变体中观察到的所有依赖氨的氨基甲酸酯磷酸酯合成均归因于乙酰激酶部分中的蛋白质,大概是乙酰激酶本身,因为乙酰磷酸酶本身与氨基甲酸酯磷酸酯的合成被平行抑制。在野生型生物中,即使添加了足够的抗体以最大程度地抑制乙酰激酶,也只能部分抑制氨依赖性活性。建议该残基是由于谷氨酰胺依赖性氨基甲酸酯磷酸合成酶所致,因为所报道的两种野生型生物体细胞提取物中存在的对抗体敏感的氨敏感的抗体不敏感的抗体的比例与抗体的水平在质量上成正比。相对于乙酰激酶存在的氨基甲酸酯磷酸合成酶。

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