Ryu S, Labbe R G
Department of Food Science, University of Massachusetts, Amherst 01003.
J Gen Microbiol. 1989 Nov;135(11):3109-18. doi: 10.1099/00221287-135-11-3109.
Coat proteins from mature spores of two enterotoxin-positive (Ent+) and two enterotoxin-negative (Ent-) strains of Clostridium perfringens were solubilized using 50 mM-dithiothreitol and 1% sodium dodecyl sulphate at pH 9.7, and alkylated using 110 mM-iodoacetamide to prevent aggregation. The coat proteins and C. perfringens type A enterotoxin (CPE) were separated by SDS-PAGE and analysed by Western blotting using anti-CPE antibody. As previously reported, CPE aggregated in the presence of SDS, but no aggregation occurred at concentrations below 15 micrograms CPE ml-1. Two CPE-related proteins (34 and 48 kDa) were found in the solubilized spore coat protein of Ent+ strains while only the 48 kDa CPE-related protein was found in the spore coat fraction of Ent- strains. CPE-related proteins comprised 2.7% and 0.8% of the total solubilized coat protein of Ent+ and Ent- strains respectively. CPE-related proteins could be extracted from the spores with 1% SDS alone. They could also be released by disruption of whole spores, indicating that the CPE-related proteins may be in the spore core or trapped between the core and coat layers. The results suggest that CPE is not a major structural component of the coat fraction of C. perfringens spores.
使用50 mM二硫苏糖醇和1%十二烷基硫酸钠在pH 9.7条件下溶解产气荚膜梭菌两种产肠毒素阳性(Ent+)菌株和两种产肠毒素阴性(Ent-)菌株成熟孢子的外壳蛋白,并用110 mM碘乙酰胺进行烷基化处理以防止聚集。通过SDS-PAGE分离外壳蛋白和A型产气荚膜梭菌肠毒素(CPE),并使用抗CPE抗体通过蛋白质免疫印迹法进行分析。如先前报道,CPE在SDS存在下会聚集,但在浓度低于15微克CPE/毫升时不会发生聚集。在Ent+菌株溶解的孢子外壳蛋白中发现了两种与CPE相关的蛋白(34 kDa和48 kDa),而在Ent-菌株的孢子外壳组分中仅发现了48 kDa与CPE相关的蛋白。与CPE相关的蛋白分别占Ent+和Ent-菌株总溶解外壳蛋白的2.7%和0.8%。与CPE相关的蛋白可以仅用1% SDS从孢子中提取出来。它们也可以通过破坏完整孢子而释放出来,这表明与CPE相关的蛋白可能存在于孢子核心或被困在核心与外壳层之间。结果表明,CPE不是产气荚膜梭菌孢子外壳组分的主要结构成分。