Miyazaki W, Tamaoka H, Shinohara M, Kaise H, Izawa T, Nakano Y, Kinoshita T, Hong K, Inoue K
Microbiol Immunol. 1980;24(11):1091-108. doi: 10.1111/j.1348-0421.1980.tb02914.x.
A complement inhibitor, K-76, was isolated and purified from the culture supernatant of a fungus, Stachybotrys complementi, nov. sp. K-76, isolated from soil of Ishigaki Island, Okinawa. K-76 is a sesquiterpene compound and it can be oxidized to a monocarboxylic derivative (K-76 COOH), the sodium salt of which is very soluble and much less toxic than K-76. K-76 and K-76 COOH both inhibited complement activation by either the classical or alternative pathway. They inhibited generation of the factor chemotactic to human polymorphonuclear leukocytes from human serum by aggregated immunoglobulin. When sensitized erythrocytes were treated with complement in the presence of K-76 COOH, the resulting unlysed cells were found to be in the state of EACl, 4b, 2a, 3b. Thus K-76 COOH is considered to block mainly the C5 intermediate step. K-76 COOH did not inhibit any proteases or esterases tested, except when tested at high concentration.
一种补体抑制剂K-76,是从冲绳石垣岛土壤中分离得到的一种新的真菌——葡萄穗霉补体霉(Stachybotrys complementi)nov. sp. K-76的培养上清液中分离纯化出来的。K-76是一种倍半萜化合物,可被氧化为单羧酸衍生物(K-76 COOH),其钠盐极易溶解,毒性比K-76小得多。K-76和K-76 COOH均可通过经典途径或替代途径抑制补体激活。它们抑制了聚集免疫球蛋白从人血清中产生对人多形核白细胞有趋化作用的因子。当用补体在K-76 COOH存在的情况下处理致敏红细胞时,发现产生的未裂解细胞处于EACl、4b、2a、3b状态。因此,K-76 COOH被认为主要阻断C5中间步骤。K-76 COOH除了在高浓度测试时外,没有抑制任何测试的蛋白酶或酯酶。