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Appl Environ Microbiol, June 1998, p. 2141-2146, Vol. 64, No. 6
Department of Soil and Environmental
Sciences, University of California, Riverside, California 92521
Received 20 November 1997/Accepted 3 April 1998
1,1-Dichloro-2,2-bis(4-chlorophenyl)ethylene (DDE), a toxic
breakdown product of 1,1,1-trichloro-2,2-bis(4-chlorophenyl)ethane (DDT), has traditionally been viewed as a dead-end metabolite: there
are no published reports detailing enzymatic ring fission of DDE by
bacteria in either soil or pure culture. In this study, we investigated
the ability of Pseudomonas acidovorans M3GY to transform
DDE and its unchlorinated analog, 1,1-diphenylethylene (DPE). While
strain M3GY could grow on DPE, cells grown on DPE as a sole carbon
source could not degrade DDE. Cells grown on biphenyl, however, did
degrade DDE. Mass balance analysis of [14C]DDE showed
transformation of more than 40% of the recoverable radioactivity. Nine
chlorinated metabolites produced from DDE were identified by gas
chromatography-mass spectrometry-Fourier-transform infrared
spectrometry (GC-MS-FTIR) from cultures grown on biphenyl. Recovery of
these metabolites demonstrates that biphenyl-grown cells degrade DDE
through a meta-fission pathway. This study provides a
possible model for biodegradation of DDE in soil by biphenyl-utilizing bacteria.
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Cometabolism of
1,1-Dichloro-2,2-Bis(4-Chlorophenyl)Ethylene by Pseudomonas
acidovorans M3GY Grown on Biphenyl
and
*
Corresponding author. Mailing address: Department of
Plant Pathology, 2268 Geology Building, University of California,
Riverside, CA 92521-0424. Phone: (909) 787-3446. Fax: (909) 787-3599. E-mail: Focht{at}CITRUS.UCR.EDU.
Present address: Center for Environmental Biotechnology, University
of Tennessee, Knoxville, Knoxville, TN 37996-1605.
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