Sakurai J, Fujii Y
Department of Microbiology, Faculty of Pharmaceutical Sciences, Tokushima Bunri University, Japan.
Toxicon. 1987;25(12):1301-10. doi: 10.1016/0041-0101(87)90008-0.
A new procedure for the purification of beta toxin from culture supernatant fluid of Clostridium perfringens was established. The procedure consists of ammonium sulfate fractionation, affinity chromatography on zinc-chelate Sepharose and gel filtration on Toyopearl HW 60. Beta toxin was purified about 460-fold from the ammonium sulfate fraction with a yield of about 60% in terms of lethality of the toxin. The molecular weight of the toxin, determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and sucrose gradient centrifugation, was approximately 40,000. The isoelectric point was 5.6. The minimal necrotic dose for guinea pigs was approximately 2 ng. The 50% lethal doses for adult mice were 310 ng/kg and 4.5 micrograms/kg, when injected i.v. and i.p., respectively.
建立了一种从产气荚膜梭菌培养上清液中纯化β毒素的新方法。该方法包括硫酸铵分级分离、锌螯合琼脂糖亲和层析和Toyopearl HW 60凝胶过滤。以毒素致死率计算,β毒素从硫酸铵分级分离物中纯化了约460倍,产率约为60%。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和蔗糖梯度离心法测定,该毒素的分子量约为40,000。其等电点为5.6。豚鼠的最小坏死剂量约为2纳克。成年小鼠静脉注射和腹腔注射时的半数致死剂量分别为310纳克/千克和4.5微克/千克。