Dreyfus L A, Frantz J C, Robertson D C
Infect Immun. 1983 Nov;42(2):539-48. doi: 10.1128/iai.42.2.539-548.1983.
Five heat-stable enterotoxins (STs) produced by enterotoxigenic Escherichia coli strains of porcine, bovine, and human host origins have been purified to apparent homogeneity. The STs with biological activity in suckling mice and piglets (STaS) contained 18 amino acid residues, 10 amino acids with a high proportion of acidic amino acids, and 6 half-cystines. The carboxy-terminal and amino-terminal residues of all STaS were tyrosine and asparagine, respectively. All five STa preparations were homogeneous by several criteria: (i) a single symmetrical peak on gel filtration, (ii) a single fluorescent band on sodium dodecyl sulfate-polyacrylamide gel electrophoresis, (iii) single carboxyl-terminal and amino-terminal residues, and (iv) amino acid analysis data that indicated a stoichiometric relationship between the component amino acids. The isoelectric points of the five STaS ranged from 3.88 to 4.08. All five purified preparations were heat stable and not denatured by organic solvents, detergents, or treatment at pH 1, but were partially inactivated after incubation at pH 12.0. Biological activity was completely abolished by treatment with reducing and oxidizing agents, which suggested that one or more disulfide bonds play an important role in the mechanism of action of STaS. Antisera raised against strain 431 STa, produced by a porcine class II enterpathogen, neutralized homologous 431 STa as well as heterologous purified STa preparations. The antiserum was used as a reagent in a sensitive radioimmunoassay to detect suckling mouse-positive strains of enterotoxigenic E. coli.
从猪、牛和人类宿主源的产肠毒素大肠杆菌菌株中产生的五种热稳定肠毒素(STs)已被纯化至表观均一。在乳鼠和仔猪中具有生物活性的STs(STaS)含有18个氨基酸残基、10个酸性氨基酸比例较高的氨基酸以及6个半胱氨酸。所有STaS的羧基末端和氨基末端残基分别为酪氨酸和天冬酰胺。通过以下几个标准,所有五种STa制剂都是均一的:(i)凝胶过滤上的单个对称峰;(ii)十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳上的单个荧光带;(iii)单个羧基末端和氨基末端残基;(iv)氨基酸分析数据表明组成氨基酸之间存在化学计量关系。五种STaS的等电点范围为3.88至4.08。所有五种纯化制剂均具有热稳定性,不会被有机溶剂、去污剂或pH 1处理变性,但在pH 12.0孵育后会部分失活。用还原剂和氧化剂处理可完全消除生物活性,这表明一个或多个二硫键在STaS的作用机制中起重要作用。针对猪II类肠道病原体产生的431 STa菌株产生的抗血清,可中和同源的431 STa以及异源纯化的STa制剂。该抗血清用作灵敏放射免疫测定中的试剂,以检测产肠毒素大肠杆菌的乳鼠阳性菌株。