Janicki B W, Wright G L, Good R C, Chaparas S D
Infect Immun. 1976 Feb;13(2):425-37. doi: 10.1128/iai.13.2.425-437.1976.
Comparisons were made of the yield, chemical content, and biological activity of filtrates and extracts obtained by sonic and pressure cell disruption of bacilli from 4- and 8-week-old Proskauer and Beck cultures of the H37Rv strain (TMC no. 102) of Mycobacterium tuberculosis. The culture filtrates were dialyzed, freeze-dried, reconstituted in saline, and sterilized by membrane filtration. The viable bacilli were washed and resuspended in distilled water and subsequently disrupted either by sonication in the cold for 15 or 30 min or by treatment at 20,000 or 40,000 lb/in2 in a pressure cell. The resulting extracts were clarified by centrifugation, concentrated, and sterilized by filtration. All preparations were adjusted to contain 10 mg of solids (dry weight)/ml and were analyzed quantitatively for protein, deoxyribonucleic acid, ribonucleic acid, polysaccharide, and lipid content. Separation patterns obtained by gradient acrylamide gel electrophoresis, as well as by one- and two-dimensional immunoelectrophoresis, provided the basis for qualitative comparisons of the culture filtrates and cell extracts. Three-point dose-response curves also were used to compare the preparations for skin test reactivity in BCG-vaccinated guinea pigs. It was concluded that, although there were no consistent differences in chemical content or biological activity between the preparations, a 15-min sonic treatment appeared to be the most suitable method for preparation of bacillary extracts based on yield of active components and ease of preparation.
对通过超声和压力细胞破碎法从结核分枝杆菌H37Rv菌株(TMC编号102)的4周龄和8周龄普罗斯考尔和贝克培养物中获得的滤液和提取物的产量、化学组成和生物活性进行了比较。培养滤液经过透析、冻干、用生理盐水复溶并通过膜过滤灭菌。将活的杆菌洗涤并重悬于蒸馏水中,随后在冷条件下超声处理15或30分钟,或在压力细胞中以20,000或40,000磅/平方英寸的压力处理进行破碎。所得提取物通过离心澄清、浓缩并通过过滤灭菌。所有制剂均调整为含有10毫克固体(干重)/毫升,并对蛋白质、脱氧核糖核酸、核糖核酸、多糖和脂质含量进行定量分析。通过梯度丙烯酰胺凝胶电泳以及一维和二维免疫电泳获得的分离模式为培养滤液和细胞提取物的定性比较提供了基础。还使用三点剂量反应曲线比较了这些制剂在卡介苗接种的豚鼠中的皮肤试验反应性。得出的结论是,尽管制剂之间在化学组成或生物活性方面没有一致的差异,但基于活性成分的产量和制备的简易性,15分钟的超声处理似乎是制备杆菌提取物的最合适方法。