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不同分子大小的C型和D型肉毒梭菌毒素的口服毒性

Oral toxicities of Clostridium botulinum type C and D toxins of different molecular sizes.

作者信息

Ohishi I, Sakaguchi G

出版信息

Infect Immun. 1980 May;28(2):303-9. doi: 10.1128/iai.28.2.303-309.1980.

Abstract

Clostridium botulinum type C progenitor toxins of different molecule sizes, C-L (16S) and C-M (12S), were purified from cultures of strains 573, Stockholm, and CB-19. C-L toxin showed some hemaggglutinin activity, whereas C-M toxin did not. Neither C-L nor C-M toxin was activated upon trypsinization. Molecular dissociation of purified type C-L and C-M toxins into toxic and nontoxic components was demonstrated by sucrose density gradient ultracentrifugation and diethylaminoethyl-Sephadex chromatography at pH 8.0. The molecular construction of type C progenitor toxin appears to be analogous to that reported for botulinum toxins of other types. C-L and D-L toxins showed higher oral toxicities to mice than did C-M or D-M toxin. Such higher oral toxicities were ascribed to the higher stabilities of these toxins in gastric and intestinal juices.

摘要

从573株、斯德哥尔摩株和CB - 19株的培养物中纯化出了不同分子大小的C型肉毒梭菌前体毒素,即C - L(16S)和C - M(12S)。C - L毒素表现出一些血凝活性,而C - M毒素则没有。C - L毒素和C - M毒素经胰蛋白酶处理后均未被激活。通过蔗糖密度梯度超速离心和在pH 8.0条件下的二乙氨基乙基 - 葡聚糖凝胶色谱法,证明了纯化的C - L型和C - M型毒素分子解离为毒性和非毒性成分。C型前体毒素的分子结构似乎与其他类型肉毒毒素所报道的结构类似。C - L毒素和D - L毒素对小鼠的口服毒性高于C - M毒素或D - M毒素。这种较高的口服毒性归因于这些毒素在胃液和肠液中的较高稳定性。

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