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从蛙肝中制备结晶氨甲酰磷酸合成酶-I

Preparation of crystalline carbamyl phosphate synthetase-I from frog liver.

作者信息

Mori M, Cohen P P

出版信息

J Biol Chem. 1978 Nov 25;253(22):8337-9.

PMID:213431
Abstract

Ammonia- and N-acetylglutamate-dependent carbamyl phosphate synthetase-I (EC 2.7.2.5), the mitchondrial enzyme involved in the initial step of urea biosynthesis, was purified to homogeneity from frog liver and crystallized. The purification involved extraction of a particulate fraction with cetyltrimethylammonium bromide in the presence of the protease inhibitors antipain, leupeptin, chymostatin, and pepstatin; acetone precipitation; and affinity chromatography with Cibacron blue F3GA-coupled agarose. The enzyme was adsorbed to the gel at pH 8.3 in the presence of 5 mM MgCl2 and eluted with magnesoum-free buffer. The enzyme crystallized as either elongated, thin, rectangular plates or as clusters of small crystals from 37 to 40% saturated ammonium sulfate. The enzyme moved as a single polypeptide band on sodium dodecyl sulfate/polyacrylamide gel electrophoresis with a molecular weight of 160,000. In the absence of protease inhibitors, proteolysis of the enzyme occurred with the formation of an enzymatically active fragment with a subunit molecular weight of 139,000.

摘要

氨和N-乙酰谷氨酸依赖性氨基甲酰磷酸合成酶-I(EC 2.7.2.5)是参与尿素生物合成第一步的线粒体酶,从蛙肝中纯化至同质并结晶。纯化过程包括在蛋白酶抑制剂抑肽酶、亮抑肽酶、糜蛋白酶抑制剂和胃蛋白酶抑制剂存在的情况下,用十六烷基三甲基溴化铵提取颗粒部分;丙酮沉淀;以及用Cibacron blue F3GA偶联琼脂糖进行亲和色谱。在5 mM MgCl2存在下,酶在pH 8.3时吸附到凝胶上,并用无镁缓冲液洗脱。该酶从37%至40%饱和硫酸铵中结晶为细长的薄矩形板或小晶体簇。在十二烷基硫酸钠/聚丙烯酰胺凝胶电泳上,该酶作为单一多肽带移动,分子量为160,000。在没有蛋白酶抑制剂的情况下,酶发生蛋白水解,形成亚基分子量为139,000的酶活性片段。

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Cell-free translation and thyroxine induction of carbamyl phosphate synthetase I messenger RNA in tadpole liver.
Proc Natl Acad Sci U S A. 1979 Jul;76(7):3179-83. doi: 10.1073/pnas.76.7.3179.

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