Muto N, Tani S
J Biochem. 1979 May;85(5):1143-9.
Two pepsinogens, the contents of which increase with developmental progress, were purified from the gastric mucosa of the adult rat by ammonium sulfate fractionation and chromatography on DEAE-cellulose and DEAE-Sepharose CL-6B columns. The purified zymogens, designated as pepsinogens I and II, were each shown to be homogeneous by polyacrylamide gel disc electrophoresis. Pepsinogen II had a greater electrophoretic mobility toward the anode at pH 8.0 than pepsinogen I. The molecular weights of both zymogens were estimated to be 38,000 by SDS-polyacrylamide gel electrophoresis. The activated enzymes, pepsins I and II, each had the same molecular weight of 32,000. The pH optima for both enzymes were found to be 2.0. The enzymes showed high stabilities at pH 8.0, while they lost their activities within 60 min at pH 10.0. The enzymes were inhibited by pepstatin and diazoacetyl-DL-norleucine methyl ester (DAN). The activities of the enzymes in hydrolyzing N-acetyl-L-phenylalanyl-3,5-diiodo-L-tyrosine (APDT) were about 1/8 of that of porcine pepsin. These results suggest that pepsins I and II are very similar.
通过硫酸铵分级分离以及在DEAE - 纤维素和DEAE - 琼脂糖CL - 6B柱上进行层析,从成年大鼠胃黏膜中纯化出两种胃蛋白酶原,其含量随发育进程增加。纯化后的酶原,分别命名为胃蛋白酶原I和胃蛋白酶原II,经聚丙烯酰胺凝胶圆盘电泳显示均为单一成分。在pH 8.0时,胃蛋白酶原II向阳极的电泳迁移率比胃蛋白酶原I大。通过SDS - 聚丙烯酰胺凝胶电泳估计两种酶原的分子量均为38,000。活化后的酶,胃蛋白酶I和胃蛋白酶II,分子量均为32,000。发现两种酶的最适pH均为2.0。这些酶在pH 8.0时具有高稳定性,而在pH 10.0时60分钟内即失去活性。这些酶被胃蛋白酶抑制剂和重氮乙酰 - DL - 正亮氨酸甲酯(DAN)抑制。它们水解N - 乙酰 - L - 苯丙氨酰 - 3,5 - 二碘 - L - 酪氨酸(APDT)的活性约为猪胃蛋白酶的1/8。这些结果表明胃蛋白酶I和胃蛋白酶II非常相似。