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OXIDATIVE MUTAGENICITY OF POLAR FRACTIONS FROM POLYCYCLIC AROMATIC HYDROCARBON-CONTAMINATED SOILS

机译:多环芳烃被土壤污染的极性馏分的氧化性

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Soils at hazardous waste sites contain complex mixtures of chemicals and often are difficult to characterize in terms of risk to human and ecological health. Over time, biogeochemical processes can decrease the apparent concentrations of pollutants but also can lead to accumulation of new products for which toxicity and behavior in the environment are largely unknown. A bioassay-directed fractionation technique was used to assess the contribution of redox-active bacterial metabolites to the toxicity of soil contaminated with polycyclic aromatic hydrocarbons (PAHs). A reverse mutation assay with Escherichia coli WP2 uvrA/ pKMlOl (IC188) and E. coli WP2 uvrA axyR/pKM101 (IC203) was used to screen fractions for genotoxicity. Strain IC203 carries the ΔoxyR30 mutation, which prevents the expression of antioxidant proteins in response to oxidative stress and increases its reversion by compounds that generate reactive oxygen species (ROS). Polar fractions of PAH-contaminated soil extracts were mutagenic to strain IC203 but not to strain IC188, suggesting the involvement of ROS in genotoxicity. Genotoxic potencies ranged from 300 to 1,700 revertants per milligram of fraction. Catalase was able to decrease IC203 reversion, implicating the involvement of hydrogen peroxide as a key ROS. Oxidized PAH compounds, including quinones, were identified in the mutagenic fractions but were not by themselves mutagenic. Deasphalted whole extracts and recombined fractions were not mutagenic, indicating that interactions between compounds in different fractions can mitigate genotoxicity.
机译:危险废物现场的土壤含有复杂的化学混合物,通常难以确定对人类和生态健康的风险。随着时间的流逝,生物地球化学过程会降低污染物的表观浓度,但也会导致新产品的积累,而这些新产品的环境毒性和行为在很大程度上是未知的。生物测定导向的分馏技术用于评估氧化还原活性细菌代谢产物对被多环芳烃(PAHs)污染的土壤毒性的贡献。使用大肠杆菌WP2 uvrA / pKM101(IC188)和大肠杆菌WP2 uvrA axyR / pKM101(IC203)进行的反向突变分析可用于筛选组分的遗传毒性。菌株IC203带有ΔoxyR30突变,该突变可防止抗氧​​化蛋白响应氧化应激而表达,并通过产生活性氧(ROS)的化合物提高其回复率。污染PAH的土壤提取物的极性级分对IC203菌株具有诱变作用,而对IC188菌株则不诱变,表明ROS参与了基因毒性。遗传毒性效力范围为每毫克级分300至1,700个还原剂。过氧化氢酶能够降低IC203的还原,暗示过氧化氢是关键的ROS。在诱变级分中鉴定出氧化的PAH化合物(包括醌),但本身不是诱变的。脱沥青的全提取物和重组馏分不具有致突变性,表明不同馏分中化合物之间的相互作用可以减轻遗传毒性。

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