Yutsudo T, Honda T, Miwatani T, Takeda Y
Microbiol Immunol. 1986;30(11):1115-27. doi: 10.1111/j.1348-0421.1986.tb03041.x.
Shiga toxin was purified from the culture supernatant of Shigella dysenteriae 1 by ammonium sulfate fractionation, DEAE-cellulose column chromatography and repeated chromatofocusing column chromatography. About 1.6 mg of purified Shiga toxin was obtained from 15 liters of culture with a yield of about 27%. The molecular weight of purified Shiga toxin was estimated to be 62,000. The toxin consisted of A and B subunits with molecular weights of about 30,000 and 5,000-6,000, respectively. The isoelectric point of purified Shiga toxin was 7.0. Purified Shiga toxin showed the following biological activities: lethal toxicity to mice when injected intraperitoneally with an LD50 of 28 ng per mouse; cytotoxicity to Vero cells, killing about 50% of the cells at 1 pg and all of the cells at 10 pg; and fluid accumulation in rabbit ileal loops at a concentration of more than 1 microgram.
通过硫酸铵分级沉淀、DEAE - 纤维素柱色谱和反复的聚焦柱色谱法,从痢疾志贺氏菌1型的培养上清液中纯化志贺毒素。从15升培养物中获得了约1.6毫克纯化的志贺毒素,产率约为27%。纯化的志贺毒素的分子量估计为62,000。该毒素由A和B亚基组成,分子量分别约为30,000和5,000 - 6,000。纯化的志贺毒素的等电点为7.0。纯化的志贺毒素表现出以下生物学活性:腹腔注射时对小鼠具有致死毒性,半数致死量为每只小鼠28纳克;对Vero细胞具有细胞毒性,在1皮克时杀死约50%的细胞,在10皮克时杀死所有细胞;在兔回肠袢中,浓度超过1微克时会引起液体蓄积。