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首页> 外文期刊>Infection and immunity >Oral toxicities of Clostridium botulinum type C and D toxins of different molecular sizes.
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Oral toxicities of Clostridium botulinum type C and D toxins of different molecular sizes.

机译:不同分子大小的C型和D型肉毒梭菌毒素的口服毒性。

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摘要

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.
机译:从菌株573,Stockholm和CB-19的培养物中纯化出不同分子大小的C-L肉毒梭状芽孢杆菌C-L(16S)和C-M(12S)毒素。 C-L毒素表现出一定的血凝素活性,而C-M毒素则没有。胰蛋白酶消化后,C-L和C-M毒素均未激活。通过蔗糖密度梯度超速离心和pH 8.0的二乙氨基乙基-Sephadex色谱法证明了纯化的C-L和C-M型毒素分子解离为有毒和无毒成分。 C型祖毒素的分子结构似乎与报道的其他类型肉毒杆菌毒素的分子结构相似。 C-L和D-L毒素对小鼠的口服毒性比C-M或D-M毒素高。如此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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