Fan'kovskaia M K, Ezepchuk Iu V, Solov'eva M N, Shcheglovitova O N
Mol Gen Mikrobiol Virusol. 1987 Jul(7):23-7.
A method is proposed for isolation and purification of the staphylococcal toxin causing the toxic shock syndrome (TSS). The method includes three steps: aggregation of protein from the cultural filtrate of Staphylococcus aureus strain 1169 in the presence of 0.025% sodium hexametaphosphate at pH 3.0; gel filtration of the concentrated material on the sephadex G75; ion-exchange chromatography on DEAE 32 cellulose. The proposed method permits to obtain the purified biologically active preparation of toxin with the yield about 40%. The obtained preparations are homogeneous in polyacrylamide electrophoresis and as analyzed by immunochemical methods. The mol mass of the isolated protein is 24 kD, it is not immunologically identical to staphylococcal toxins A-D and is lethal for New Zealand white rabbits and chinchilla rabbits. Interferon inducing activity of the protein is identical to the one of staphylococcal enterotoxin type A.
提出了一种分离和纯化导致中毒性休克综合征(TSS)的葡萄球菌毒素的方法。该方法包括三个步骤:在pH 3.0、0.025%六偏磷酸钠存在的条件下,使金黄色葡萄球菌1169菌株培养滤液中的蛋白质聚集;将浓缩物在葡聚糖G75上进行凝胶过滤;在DEAE 32纤维素上进行离子交换色谱。所提出的方法能够获得产率约为40%的纯化的具有生物活性的毒素制剂。所获得的制剂在聚丙烯酰胺电泳中是均一的,并且经免疫化学方法分析也是均一的。分离出的蛋白质的分子量为24 kD,它与葡萄球菌毒素A - D在免疫上不相同,并且对新西兰白兔和毛丝鼠兔具有致死性。该蛋白质的干扰素诱导活性与A型葡萄球菌肠毒素的相同。