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从支气管败血波氏杆菌超声提取物制备的皮肤坏死毒素的特性。

Properties of dermonecrotic toxin prepared from sonic extracts Bordetella bronchiseptica.

作者信息

Kume K, Nakai T, Samejima Y, Sugimoto C

出版信息

Infect Immun. 1986 May;52(2):370-7. doi: 10.1128/iai.52.2.370-377.1986.

Abstract

A toxin with dermonecrotic activity (DNT) was purified from sonic extracts of Bordetella bronchiseptica L3 of pig origin at phase I by chromatographic and electrophoretic methods. The purification procedure was one developed for obtaining the Pasteurella multocida DNT from sonic extracts with some modifications. Dermonecrotizing activity of B. bronchiseptica-purified DNT was increased by 600-fold compared with that of the crude extract, and the average yield was about 3%. The toxin was homogeneous, as determined by Ouchterlony double immunodiffusion, crossed immunoelectrophoresis, and disk isoelectric focusing in polyacrylamide gels. The toxin gave a single band on polyacrylamide disk gel electrophoresis (PAGE) and sodium dodecyl sulfate-SDS PAGE. The molecular weight of the toxin was ca. 190,000 +/- 5,000, as determined by SDS-PAGE. The isoelectric point of the toxin was ca. 6.5 to 6.6. The minimal necrotizing dose of the toxin for guinea pigs was about 2 ng of protein per 0.1 ml, the 50% lethal dose per mouse was about 0.3 micrograms, and the minimal cytotoxic dose for embryonic bovine lung cells was about 2 ng/ml. The toxin was heat labile and sensitive to inactivation by trypsin, Formalin, and glutaraldehyde. The mildly trypsinized B. bronchiseptica DNT preparation dissociated into two polypeptide chains, with molecular weights of ca. 75,000 +/- 4,000 (fragment 1) and ca. 118,000 +/- 5,000 (fragment 2), after treatment with dithiothreitol-SDS or urea. Upon removal of dithiothreitol and urea from the dissociated DNT preparation, the fragments reassociated, and the DNT that was formed was indistinguishable from the native toxin.

摘要

在第一阶段,通过色谱和电泳方法从猪源支气管败血波氏杆菌L3的超声提取物中纯化出一种具有皮肤坏死活性的毒素(DNT)。纯化程序是在从超声提取物中获取多杀巴斯德菌DNT的方法基础上进行了一些修改而开发的。与粗提物相比,支气管败血波氏杆菌纯化的DNT的皮肤坏死活性提高了600倍,平均产量约为3%。通过免疫双扩散、交叉免疫电泳和聚丙烯酰胺凝胶圆盘等电聚焦测定,该毒素是均一的。该毒素在聚丙烯酰胺圆盘凝胶电泳(PAGE)和十二烷基硫酸钠 - SDS PAGE上呈现单一条带。通过SDS - PAGE测定,该毒素的分子量约为190,000±5,000。该毒素的等电点约为6.5至6.6。该毒素对豚鼠的最小坏死剂量约为每0.1 ml 2 ng蛋白质,对小鼠的半数致死剂量约为0.3微克,对胚胎牛肺细胞的最小细胞毒性剂量约为2 ng/ml。该毒素对热不稳定,对胰蛋白酶、福尔马林和戊二醛的灭活敏感。用二硫苏糖醇 - SDS或尿素处理后,轻度胰蛋白酶处理的支气管败血波氏杆菌DNT制剂解离成两条多肽链,分子量分别约为75,000±4,000(片段1)和约118,000±5,000(片段2)。从解离的DNT制剂中去除二硫苏糖醇和尿素后,片段重新结合,形成的DNT与天然毒素无法区分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72eb/261008/08edcbe118d7/iai00104-0034-a.jpg

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