De Wolf M, Hilderson H J, Lagrou A, Dierick W
Arch Int Physiol Biochim. 1979 Feb;87(1):1-18. doi: 10.3109/13813457909070481.
Lysophospholipids are formed during phospholipid breakdown as a result of the action of phospholipases A. At certain concentrations these lysoderivatives destabilise biological membranes. Therefore, their concentration is of critical importance for membrane integrity. Prevention of lysophosphoglycerides accumulation may be the important role for lysophospholipases and is probably the explanation for their widespread occurrence in nature. Lysophospholipase activities were found in molds (Fairbairn, 1948), rice bran (Contardi & Ercoli, 1933), several microorganisms (Brockerhoff & Jensen, 1974), snake and bee venoms (Doery & Pearson, 1964; Mohamed et al., 1969; Shiloah et al., 1973), insects (Khan & Hodgson, 1967; Rao & Subrahmanyam, 1969), fish muscle (Yurkovski & Brockerhoff, 1965; Cohen et al., 1967) and in various animal tissues (Marples & Thompson, 1960). In mammalian tissue the enzyme was first described in beef pancreas (Shapiro, 1953). Relatively high levels were detected in intestine, lung, spleen, liver and pancreas, while lower levels were present in muscle, kidney, testes, brain and blood (Marples & Thompson, 1960). The presence of lysophospholipase activity in both supernatant and sediment of bovine thyroid was reported previously in relation to possible interference of this enzyme with the phospholipase A activity assay (De Wolf et al., 1976). The subcellular localization of bovine thyroid lysophospholipase and some properties of the membrane bound enzyme activity are discussed in this paper.
溶血磷脂是磷脂酶A作用导致磷脂分解过程中形成的。在特定浓度下,这些溶血衍生物会破坏生物膜的稳定性。因此,它们的浓度对于膜的完整性至关重要。预防溶血甘油磷脂的积累可能是溶血磷脂酶的重要作用,这可能也是它们在自然界广泛存在的原因。在霉菌(费尔贝恩,1948年)、米糠(孔塔尔迪和埃尔科利,1933年)、几种微生物(布罗克霍夫和詹森,1974年)、蛇毒和蜂毒(多里和皮尔逊,1964年;穆罕默德等人,1969年;希洛阿等人,1973年)、昆虫(汗和霍奇森,1967年;拉奥和苏布拉马尼亚姆,1969年)、鱼肌肉(尤尔科夫斯基和布罗克霍夫,1965年;科恩等人,1967年)以及各种动物组织(马普尔斯和汤普森,1960年)中都发现了溶血磷脂酶活性。在哺乳动物组织中,该酶最早在牛胰腺中被描述(夏皮罗,1953年)。在肠道、肺、脾脏、肝脏和胰腺中检测到相对较高的水平,而在肌肉、肾脏、睾丸、大脑和血液中含量较低(马普尔斯和汤普森,1960年)。先前有报道称,牛甲状腺的上清液和沉淀物中都存在溶血磷脂酶活性,这与该酶可能干扰磷脂酶A活性测定有关(德沃尔夫等人,1976年)。本文讨论了牛甲状腺溶血磷脂酶的亚细胞定位以及膜结合酶活性的一些特性。