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首页> 外文期刊>Teratogenesis, carcinogenesis, and mutagenesis >Analysis of the cytotoxicity and mutagenicity of drinking water disinfection by-products in Salmonella typhimurium.
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Analysis of the cytotoxicity and mutagenicity of drinking water disinfection by-products in Salmonella typhimurium.

机译:鼠伤寒沙门氏菌饮用水消毒副产物的细胞毒性和致突变性分析。

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摘要

We analyzed the cytotoxicity and mutagenicity of the drinking water disinfection by-products (DBPs) bromoform (BF), bromoacetic acid (BA), dibromoacetic acid (DBA), tribromoacetic acid (TCA), chloroform (CF), chloroacetic acid (CA), dichloroacetic acid (DCA), trichloroacetic acid (TCA), 3-chloro-4-(dichloromethyl)-5-hydroxy-2[5H]-furanone (MX), and potassium bromate (KBrO3) in Salmonella typhimurium strains TA98, TA100, and RSJ100 +/- S9. Solvent controls of DMSO and ethanol and a positive control of ethylmethanesulfonate (EMS) were also analyzed. We developed a rapid microplate-based method to determine the cytotoxicity of the DBPs and we determined their mutagenic potencies. The distributions of the rank order for the cytotoxicity and mutagenicity of these DBPs were compared and the structure-function relationships were identified. TA100 -S9 was the most sensitive strain for these DBPs. The rank order of the mutagenic potency adjusted with a cytoxicity factor was MX > BA > EMS > DBA > DCA > CA with TBA, TCA, BF, and CF not mutagenic. From a structure-function perspective, the brominated acetic acids were more cytotoxic and mutagenic than their chlorinated analogs. BA was 150x more mutagenic than CA. The mutagenic potency of the haloacetic acids was inversely related to the number of halogen atoms of the molecule. BA was 36x more mutagenic than DBA. The differential cytotoxicity expressed by the DBPs indicated that a cytotoxicity analysis enhanced the sensitivity of the mutagenicity data, which resulted in an enhanced precision for comparing their relative mutagenic strengths. This information is critical when conducting quantitative structure-function analysis of these hazardous agents.
机译:我们分析了饮用水消毒副产物(DBP)溴仿(BF),溴乙酸(BA),二溴乙酸(DBA),三溴乙酸(TCA),氯仿(CF),氯乙酸(CA)的细胞毒性和致突变性鼠伤寒沙门氏菌TA98,TA100菌株中的二氯乙酸(DCA),三氯乙酸(TCA),3-氯-4-(二氯甲基)-5-羟基-2 [5H]-呋喃酮(MX)和溴酸钾(KBrO3) ,以及RSJ100 +/- S9。还分析了DMSO和乙醇的溶剂对照以及甲烷磺酸乙酯(EMS)的阳性对照。我们开发了一种基于微孔板的快速方法来确定DBP的细胞毒性,并确定了它们的诱变能力。比较了这些DBP的细胞毒性和致突变性的等级顺序分布,并鉴定了结构-功能关系。 TA100 -S9是这些DBP最敏感的菌株。用细胞毒性因子调整的致突变力的等级顺序为MX> BA> EMS> DBA> DCA> CA,而TBA,TCA,BF和CF不致突变。从结构功能的角度来看,溴代乙酸比其氯化类似物更具细胞毒性和致突变性。 BA的诱变性比CA高150倍。卤代乙酸的诱变能力与分子中卤素原子的数量成反比。 BA的致突变性比DBA高36倍。 DBPs表达的细胞毒性差异表明,细胞毒性分析提高了诱变数据的敏感性,从而提高了比较其相对诱变强度的精度。在对这些有害物质进行定量结构-功能分析时,此信息至关重要。

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