Itami C, Taguchi R, Ikezawa H, Nakabayashi T
Laboratory of Biochemistry, Faculty of Pharmaceutical Sciences, Mukogawa Women's University, Hyogo, Japan.
Biosci Biotechnol Biochem. 1997 Feb;61(2):336-40. doi: 10.1271/bbb.61.336.
This study investigated ectoenzyme release from small intestine brush border membranes (duodenum and jejunum, Preparation A; ileum, Preparation B) of mice by the action of phosphatidylinositol-specific phospholipase C or glycosyl-phosphatidylinositol-specific phospholipase D. Most of the alkaline phosphatase was solubilized from Preparation A, but about 60% was released from Preparation B. As for alkaline phosphodiesterase I activity, 15 and 10% were released from Preparations A and B, respectively. With Preparation B, octylglucoside treatment followed by phosphatidylinositol-specific phospholipase C or glycosyl-phosphatidylinositol-specific phospholipase D completely solubilized the alkaline phosphatase activity. However, this treatment did not change the ratio of release of alkaline phosphodiesterase I from Preparation A or B. These results indicate that the resistance to alkaline phosphatase found in Preparation B is due to hindered accessibility of the bonding splitting by phosphatidylinositol-specific phospholipase C and not to a modified glycosyl-phosphatidylinositolanchor.
本研究通过磷脂酰肌醇特异性磷脂酶C或糖基磷脂酰肌醇特异性磷脂酶D的作用,研究了小鼠小肠刷状缘膜(十二指肠和空肠,制剂A;回肠,制剂B)中外切酶的释放情况。大部分碱性磷酸酶从制剂A中溶解,但约60%从制剂B中释放。至于碱性磷酸二酯酶I活性,分别从制剂A和B中释放出15%和10%。对于制剂B,用辛基葡糖苷处理后再用磷脂酰肌醇特异性磷脂酶C或糖基磷脂酰肌醇特异性磷脂酶D可完全溶解碱性磷酸酶活性。然而,这种处理并没有改变制剂A或B中碱性磷酸二酯酶I的释放比例。这些结果表明,制剂B中对碱性磷酸酶的抗性是由于磷脂酰肌醇特异性磷脂酶C阻碍了键断裂的可及性,而不是由于糖基磷脂酰肌醇锚的修饰。