Heitkamp M A, Freeman J P, Miller D W, Cerniglia C E
National Center for Toxicological Research, Food and Drug Administration, Jefferson, Arkansas 72079.
Appl Environ Microbiol. 1988 Oct;54(10):2556-65. doi: 10.1128/aem.54.10.2556-2565.1988.
The degradation of pyrene, a polycyclic aromatic hydrocarbon containing four aromatic rings, by pure cultures of a Mycobacterium sp. was studied. Over 60% of [14C]pyrene was mineralized to CO2 after 96 h of incubation at 24 degrees C. High-pressure liquid chromatography analyses showed the presence of one major and at least six other metabolites that accounted for 95% of the total organic-extractable 14C-labeled residues. Analyses by UV, infrared, mass, and nuclear magnetic resonance spectrometry and gas chromatography identified both pyrene cis- and trans-4,5-dihydrodiols and pyrenol as initial microbial ring-oxidation products of pyrene. The major metabolite, 4-phenanthroic acid, and 4-hydroxyperinaphthenone and cinnamic and phthalic acids were identified as ring fission products. 18O2 studies showed that the formation of cis- and trans-4,5-dihydrodiols were catalyzed by dioxygenase and monooxygenase enzymes, respectively. This is the first report of the chemical pathway for the microbial catabolism of pyrene.
研究了一株分枝杆菌属细菌的纯培养物对含有四个芳香环的多环芳烃芘的降解情况。在24℃下培养96小时后,超过60%的[14C]芘被矿化为二氧化碳。高压液相色谱分析表明,存在一种主要代谢物以及至少六种其他代谢物,它们占可通过有机萃取的14C标记残留物总量的95%。通过紫外、红外、质谱、核磁共振光谱以及气相色谱分析,确定芘顺式和反式-4,5-二氢二醇以及芘醇为芘的初始微生物环氧化产物。主要代谢物4-菲甲酸、4-羟基苊醌以及肉桂酸和邻苯二甲酸被确定为环裂解产物。18O2研究表明,顺式和反式-4,5-二氢二醇的形成分别由双加氧酶和单加氧酶催化。这是关于芘微生物分解代谢化学途径的首次报道。