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小肠在从谷氨酸合成精氨酸过程中不可或缺的酶学证据。I. 吡咯啉-5-羧酸合酶

Enzymological evidence for the indispensability of small intestine in the synthesis of arginine from glutamate. I. Pyrroline-5-carboxylate synthase.

作者信息

Wakabayashi Y, Yamada E, Hasegawa T, Yamada R

机构信息

Department of Biochemistry, Kyoto Prefectural University of Medicine, Japan.

出版信息

Arch Biochem Biophys. 1991 Nov 15;291(1):1-8. doi: 10.1016/0003-9861(91)90097-3.

Abstract

The in vivo synthesis of arginine from glutamate in mammals requires seven enzymes to cooperate. Pyrroline-5-carboxylate synthase (PCS) is the first enzyme required. In order to establish the interorgan dependency of arginine synthesis, we quantitated PCS activity in as many as 32 rat tissues and found that the activity was concentrated only in the upper small intestine. Minor activity was found in pancreas, thymus, lymph node, and some other tissues: this was confirmed by the dependency on specific substrates, the loss of activity in the presence of an inhibitor, and identifying the reduced product as proline. No difference in activity was found between male and female rats on a milligram protein basis. The strict tissue localization of PCS and the localization of other enzymes of arginine synthesis previously reported clearly indicate that the upper small intestine is an indispensable tissue for the arginine synthesis from glutamate. Many of the tissues examined showed an activity to form an unknown product from glutamate. When assayed by the previously reported radiometric assay procedure using an AG1-X8 column (acetate), the product was not separated from PC and caused false-positive activities of PCS. An improved procedure was developed to overcome this technical difficulty. The new procedure enabled us to detect even 20 pmol PC without contamination by the adjoining unknown product. A preliminary characterization of the unknown product was achieved.

摘要

在哺乳动物体内,从谷氨酸合成精氨酸需要七种酶协同作用。吡咯啉-5-羧酸合酶(PCS)是所需的第一种酶。为了确定精氨酸合成的器官间依赖性,我们对多达32种大鼠组织中的PCS活性进行了定量,发现该活性仅集中在上段小肠。在胰腺、胸腺、淋巴结和其他一些组织中发现了少量活性:这通过对特定底物的依赖性、抑制剂存在时活性的丧失以及将还原产物鉴定为脯氨酸得到了证实。以毫克蛋白为基础,雄性和雌性大鼠之间未发现活性差异。PCS的严格组织定位以及先前报道的精氨酸合成其他酶的定位清楚地表明,上段小肠是从谷氨酸合成精氨酸不可或缺的组织。许多检测的组织显示出从谷氨酸形成未知产物的活性。当使用AG1-X8柱(醋酸盐)通过先前报道的放射性测定程序进行检测时,产物未与脯氨酸分离,并导致PCS出现假阳性活性。为克服这一技术难题,开发了一种改进的程序。新程序使我们能够检测到低至20 pmol的脯氨酸,而不会受到相邻未知产物的污染。对未知产物进行了初步表征。

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