National Center for Toxicological Research, Food and Drug Administration, Jefferson, Arkansas 72079.
Appl Environ Microbiol. 1991 Mar;57(3):636-41. doi: 10.1128/aem.57.3.636-641.1991.
A Mycobacterium sp. previously isolated from oil-contaminated estuarine sediments was capable of extensively mineralizing the high-molecular-weight polycyclic aromatic hydrocarbon fluoranthene. A carboxylic acid metabolite accumulated and was isolated by thin-layer and high-pressure liquid chromatographic analyses of ethyl acetate extracts from acidified culture media. The metabolite reached a maximum concentration of approximately 0.65% after 24 h of incubation. On the basis of comparisons with authentic compound in which we used UV and fluorescence spectrophotometry and R(f) values, as well as mass spectral and proton and carbon nuclear magnetic resonance spectral analyses, the metabolite was identified as 9-fluorenone-1-carboxylic acid. This is the first report in a microbial system of a fluoranthene metabolite in which significant degradation of one of the aromatic rings has occurred.
先前从受石油污染的河口沉积物中分离出的分枝杆菌属(Mycobacterium sp.)能够广泛矿化高分子量多环芳烃荧蒽。通过对酸化培养基中乙酸乙酯提取物进行薄层层析和高压液相色谱分析,积累并分离出一种羧酸代谢物。在 24 小时的孵育后,代谢物的浓度达到了约 0.65%的最大值。基于与我们使用紫外和荧光分光光度法以及 R(f) 值以及质谱和质子和碳核磁共振谱分析的纯化合物的比较,鉴定出代谢物为 9-芴酮-1-羧酸。这是在微生物系统中首次报道发生了一个芳环的显著降解的荧蒽代谢物。