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Applied and Environmental Microbiology, September 2006, p. 6034-6039, Vol. 72, No. 9
0099-2240/06/$08.00+0 doi:10.1128/AEM.00897-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Department of Microbiology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand,1 National Research Center for Environmental and Hazardous Waste Management (NRC-EHWM), Faculty of Science, Chulalongkorn University, Bangkok, Thailand,2 Department of Chemistry, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand3
Received 17 April 2006/ Accepted 18 July 2006
The acenaphthylene-degrading bacterium Rhizobium sp. strain CU-A1 was isolated from petroleum-contaminated soil in Thailand. This strain was able to degrade 600 mg/liter acenaphthylene completely within three days. To elucidate the pathway for degradation of acenaphthylene, strain CU-A1 was mutagenized by transposon Tn5 in order to obtain mutant strains deficient in acenaphthylene degradation. Metabolites produced from Tn5-induced mutant strains B1, B5, and A53 were purified by thin-layer chromatography and silica gel column chromatography and characterized by mass spectrometry. The results suggested that this strain cleaved the fused five-membered ring of acenaphthylene to form naphthalene-1,8-dicarboxylic acid via acenaphthenequinone. One carboxyl group of naphthalene-1,8-dicarboxylic acid was removed to form 1-naphthoic acid which was transformed into salicylic acid before metabolization to gentisic acid. This work is the first report of complete acenaphthylene degradation by a bacterial strain.
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