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Biotransformation of fluorene by the fungus Cunninghamella elegans
J V Pothuluri1, J P Freeman, F E Evans
1National Center for Toxicological Research, Food and Drug Administration, Jefferson, Arkansas 72079.
Applied and Environmental Microbiology
|June 1, 1993
Abstract:
The metabolism of fluorene, a tricyclic aromatic hydrocarbon, by Cunninghamella elegans ATCC 36112 was investigated. Approximately 69% of the [9-14C]fluorene added to cultures was metabolized within 120 h. The major ethyl acetate-soluble metabolites were 9-fluorenone (62%), 9-fluorenol, and 2-hydroxy-9-fluorenone (together, 7.0%). Similarly to bacteria, C. elegans oxidized fluorene at the C-9 position of the five-member ring to form an alcohol and the corresponding ketone. In addition, C. elegans produced the novel metabolite 2-hydroxy-9-fluorenone.