Schoeny R, Cody T, Radike M, Warshawsky D
Environ Mutagen. 1985;7(6):839-55. doi: 10.1002/em.2860070606.
The metabolism and growth effects of benzo(a)pyrene (BaP) were studied using a freshwater green alga, Selenastrum capricornutum. Algal cultures were incubated under gold light with BaP added at concentrations of 40, 160, 400, and 1,200 micrograms/liter for the periods of 1-4 days. The metabolites and BaP were identified and quantified from ethyl acetate extracts of both algal cells and incubation medium. The ethyl acetate extracts were evaluated for genotoxicity using a micro-volume Salmonella typhimurium forward mutation assay with resistance to 8-azaguanine for selection. This assay detected the presence of small quantities of BaP and was particularly sensitive to the mutagenicity of BaP diols. Of those extracts prepared from algae and medium from cultures exposed to 400 micrograms BaP/liter (10 micrograms/25 ml culture), only algal cell extracts from one day's growth were mutagenic. In cultures exposed to 1,200 micrograms BaP/liter (30 micrograms/25 ml culture), mutagenic materials were produced or persisted in both algae and media throughout the 4-day incubation. The observed mutagenic response can be attributed in part to the presence of unmetabolized BaP or to BaP diols.
利用淡水绿藻羊角月芽藻研究了苯并(a)芘(BaP)的代谢及生长效应。将藻类培养物置于金色光照下,添加浓度为40、160、400和1200微克/升的BaP,培养1 - 4天。从藻类细胞和培养液的乙酸乙酯提取物中鉴定并定量代谢产物和BaP。使用对8 - 氮杂鸟嘌呤有抗性的微量鼠伤寒沙门氏菌正向突变试验评估乙酸乙酯提取物的遗传毒性,以此进行筛选。该试验检测到了少量BaP的存在,并且对BaP二醇的致突变性特别敏感。在暴露于400微克BaP/升(10微克/25毫升培养物)的培养物所制备的藻类和培养液提取物中,只有生长一天的藻类细胞提取物具有致突变性。在暴露于1200微克BaP/升(30微克/25毫升培养物)的培养物中,在整个4天的培养期间,藻类和培养液中均产生或残留有致突变物质。观察到的致突变反应部分可归因于未代谢的BaP或BaP二醇的存在。