微生物生物测定中影响毒物相互作用程度的因素

G. Stratton
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引用次数: 8

摘要

采用毒物相互作用方法,研究了微生物生物测定中各参数对相互作用反应的影响。采用毒琼脂技术,将最后一种真菌(Pythium ultimum)暴露于杀菌剂captan和几种有机溶剂的不同组合中。在所有情况下,杀菌剂和溶剂协同作用,促进培养生长。在大多数实验中,丙酮被用作测试溶剂。当pH和温度发生变化时,当pH从4.5℃升高到7.5℃,当温度从15℃升高到30℃时,丙酮和队长酯的相互作用响应幅度显著增加。这与培养生长率的增加和队长的毒性的降低相对应。当介质组成发生变化时,在生长速度最快的介质中,相互作用强度再次最大。这些介质也产生了最低的船长毒性。与V8果汁琼脂的相互作用最大,其次是玉米粉琼脂、马铃薯葡萄糖琼脂和麦芽提取物琼脂。当相互作用实验中使用的溶剂发生变化时,得到了类似的反应,即最大的相互作用强度发生在引起最低船长毒性的体系中。丙酮的测量值最大,其次是己烷、乙醇、二甲基甲酰胺、甲醇和二甲基亚砜。讨论了这些数据在毒物相互作用生物测定中的意义。
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Factors affecting the magnitude of toxicant interactions in microbial bioassays
A toxicant interaction method was used to study the effects of various bioassay parameters on interaction responses obtained in microbial bioassays. The fungus Pythium ultimum was employed as the test organism, and was exposed to various combinations of the fungicide captan and several organic solvents, using a poisoned agar technique. In all cases the fungicide and solvents interacted synergistically toward culture growth. For most experiments acetone was used as the test solvent. Where pH and temperature were altered, the magnitude of the interaction response between captan and acetone increased dramatically as the pH or temperature was raised from 4.5 to 7.5, or 15 to 30°C, respectively. This corresponded to similar increases in the culture growth rate and decreases in the toxicity of captan. When the medium composition was changed, interaction magnitudes were again greatest in media eliciting the fastest growth rate. These media also yielded the lowest captan toxicity. The largest interaction magnitudes occurred with V8 juice agar, followed by corn meal agar, potato dextrose agar, and malt extract agar. When the solvent used in the interaction experiments was changed, a similar response was obtained, in that the greatest interaction magnitudes occurred in systems eliciting the lowest captan toxicity. The largest magnitudes were measured with acetone, followed by hexane, ethanol, dimethylformamide, methanol, and dimethyl sulfoxide. The significance of these data in toxicant interaction bioassays is discussed.
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