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检测空气中颗粒物污染物的致突变活性。

Detection of mutagenic activity in particulate air pollutants.

作者信息

Tokiwa H, Morita K, Takeyoshi H, Takahashi K, Ohnishi Y

出版信息

Mutat Res. 1977 Apr;48(2):237-48. doi: 10.1016/0027-5107(77)90165-8.

Abstract

Ames's strains of Salmonella typhimurium were used to evaluate the mutagenic activity of airbone particulate materials collected at six different points in the industrial area of Ohmuta and the residential area Fukuoka. Tests were done in presence of rat-liver S-9 fraction isolated from rats that had been treated with Aroclor 1254. When the number of revertant colonies per plate was plotted against the amount of methanol extract of particulate air pollutants, using strain TA98, approximately linear relationships were observed for active samples. Generally, mutagenic activity of the samples increased in proportion to the density of air pollutants. In our system, 38--349 microng of methanol extract, from 0.225--4.51 m3 of air from the factory districts in Ohmuta City gave 100 his+ revertants per plate. On the other hand, 54--2300 microng of air pollutants, from 1.29--14.1 m3 of air from the residential districts in Fukuoka City, gave a comparable activity. Every sample from each area had mutagenic activity. Chemicals in air pollutants were fractionated by alumina column chromatography and identified by gas chromatography and mass spectrometry. More than 28 compounds, including 12 unknown substances were identified as polycyclic hydrocarbons. Twelve of these compounds are already known to be carcinogens and to induce reversions to histidine independence in strain TA98 of Salmonella.

摘要

利用鼠伤寒沙门氏菌的艾姆斯菌株,对在大牟田工业区和福冈居民区六个不同地点采集的空气颗粒物的致突变活性进行了评估。测试是在存在从经多氯联苯混合物1254处理的大鼠中分离得到的大鼠肝脏S - 9组分的情况下进行的。当使用TA98菌株将每平板回复突变菌落数与空气颗粒物污染物的甲醇提取物量作图时,观察到活性样品呈现近似线性关系。一般来说,样品的致突变活性与空气污染物密度成正比。在我们的系统中,从大牟田市工厂区0.225 - 4.51立方米空气中提取的38 - 349微克甲醇提取物,每平板产生100个组氨酸依赖型回复突变体。另一方面,从福冈市居民区1.29 - 14.1立方米空气中提取的54 - 2300微克空气污染物产生了类似的活性。每个区域的每个样品都有致突变活性。空气污染物中的化学物质通过氧化铝柱色谱法进行分离,并通过气相色谱和质谱法进行鉴定。包括12种未知物质在内的28种以上化合物被鉴定为多环芳烃。其中12种化合物已知是致癌物,并能在鼠伤寒沙门氏菌TA98菌株中诱导回复突变为组氨酸非依赖型。

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