RECALCITRANCE OF 1,1-DICHLORO-2,2-BIS(P-CHLOROPHENYL)ETHYLENE (DDE) TO COMETABOLIC DEGRADATION BY PURE CULTURES OF AEROBIC AND ANAEROBIC-BACTERIA

Citation
M. Megharaj et al., RECALCITRANCE OF 1,1-DICHLORO-2,2-BIS(P-CHLOROPHENYL)ETHYLENE (DDE) TO COMETABOLIC DEGRADATION BY PURE CULTURES OF AEROBIC AND ANAEROBIC-BACTERIA, Archives of environmental contamination and toxicology, 33(2), 1997, pp. 141-146
Citations number
34
Categorie Soggetti
Toxicology,"Environmental Sciences
ISSN journal
00904341
Volume
33
Issue
2
Year of publication
1997
Pages
141 - 146
Database
ISI
SICI code
0090-4341(1997)33:2<141:RO1(T>2.0.ZU;2-5
Abstract
Pure cultures of aerobic and anaerobic bacteria capable of oxidation a nd reductive dehalogenation of chloroethylenes, and aerobic bacteria i nvolved in biodegradation of polychlorinated biphenyls (PCBs) were scr eened for their ability to cometabolize the persistent pollutant 1,1-d ichloro-2,2-bis(p-chlorophenyl)ethylene (DDE). Bacterial cultures expr essing methane monooxygenase (Methylosinus trichosporium), propane mon ooxygenase (Mycobacterium vaccae) and biphenyl 2,3-dioxygenase enzymes (Pseudomonas fluorescens and Rhodococcus globerulus), as well as bact eria reductively dechlorinating chloroethylenes (Acetobacterium woodii and Clostridium butyricum) could not degrade DDE. Cell-free extracts of M. trichosporium, M. vaccae, P. fluorescens and R. globerulus were also unable to transform DDE, indicating that cell wall and membrane d iffusion barriers were not biodegradation limiting. These studies sugg est that these bacteria can not degrade DDE, even when provided with c osubstrates that induce chlorophenyl-and dichloroethylene-group transf orming enzymes.