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Appl. Environ. Microbiol., Feb 1995, 443-447, Vol 61, No. 2
JJ Arensdorf and DD Focht
Bacterial degradation of biphenyl and polychlorinated biphenyls proceeds by
a well-studied pathway which produces benzoate and 2-
hydroxypent-2,4-dienoate (or, in the case of polychlorinated biphenyls, the
chlorinated derivatives of these compounds). Pseudomonas cepacia P166
utilizes 4-chlorobiphenyl for growth and produces 4-chlorobenzoate as a
central intermediate. In this study we found that strain P166 further
transforms 4-chlorobenzoate to 4-chlorocatechol, which is mineralized by a
meta cleavage pathway. Key metabolites which we identified include the meta
cleavage product (5-chloro-2-hydroxymuconic semialdehyde),
5-chloro-2-hydroxymuconate, 5-chloro-2-oxopent-4-enoate,
5-chloro-4-hydroxy-2-oxopentanoate, and chloroacetate. Chloroacetate
accumulated transiently, and slow but stoichiometric dehalogenation was
observed.
Copyright © 1995, American Society for Microbiology
A meta cleavage pathway for 4-chlorobenzoate, an intermediate in the metabolism of 4-chlorobiphenyl by Pseudomonas cepacia P166
Environmental Toxicology Graduate Program, University of California, Riverside 92521, USA.
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