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E型肉毒杆菌毒素的热灭活

Thermal inactivation of type E botulinum toxin.

作者信息

Licciardello J J, Nickerson J T, Ribich C A, Goldblith S A

出版信息

Appl Microbiol. 1967 Mar;15(2):249-56. doi: 10.1128/am.15.2.249-256.1967.

Abstract

The theoretical required cooking times for inactivation of type E Clostridium botulinum toxin (5,000 ld(50) mouse units per 0.5 ml) in haddock fillets of various sizes were calculated by graphical integration of the toxin inactivation rate and heat penetration data. The results indicated that normal cooking procedures should suffice to inactivate this amount of toxin. This conclusion was substantiated by the following additional experimental observations which revealed that the original experiments had been conducted under conservative conditions. First, maximal heat stability of the toxin was found to occur at about pH 5.5, with decreasing resistance upon increasing pH. The theoretical cooking times were based on destruction of the toxin at pH 6.7. The pH of radio-pasteurized inoculated haddock, when toxin production had occurred, was on the alkaline side, at which condition the toxin is heat-labile. Second, when spoilage was discernible in radio-pasteurized inoculated haddock, the toxin titer was low, about 50 ld(50) mouse units per 0.5 ml. Third, the toxin was adequately inactivated in toxic fillets after deep-fat frying for 3 min at 375 F (190.6 C) or after pan frying for 5 min per side at 400 F (204.4 C). Fourth, in this study, residual toxin activity was assayed by intraperitoneal injection of mice. It was shown that the oral toxic dose was 50 to 100 times greater than the intraperitoneal toxic dose.

摘要

通过对毒素失活率和热穿透数据进行图形积分,计算出不同大小的黑线鳕鱼片灭活E型肉毒梭菌毒素(每0.5毫升含5000个半数致死量小鼠单位)所需的理论烹饪时间。结果表明,正常烹饪程序应足以灭活此量的毒素。以下额外的实验观察结果证实了这一结论,这些观察结果表明原始实验是在保守条件下进行的。首先,发现毒素的最大热稳定性出现在pH约5.5时,随着pH值升高,抵抗力下降。理论烹饪时间是基于在pH 6.7时毒素的破坏情况。接种毒素的辐射巴氏杀菌黑线鳕在产生毒素时的pH值呈碱性,在此条件下毒素对热不稳定。其次,当接种毒素的辐射巴氏杀菌黑线鳕出现明显变质时,毒素效价较低,约为每0.5毫升50个半数致死量小鼠单位。第三,毒素在375°F(190.6°C)下进行3分钟的深度油炸或在400°F(204.4°C)下每面煎5分钟后,在有毒鱼片内被充分灭活。第四,在本研究中,通过对小鼠进行腹腔注射来测定残留毒素活性。结果表明,经口毒性剂量比腹腔毒性剂量大50至100倍。

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