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Open AccessJournal ArticleDOI

Cometabolism of m-chlorobenzoate by an Arthrobacter.

R. S. Horvath, +1 more
- 01 Aug 1970 - 
- Vol. 20, Iss: 2, pp 254-258
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TLDR
The data indicate that cometabolism by the arthrobacter results from the formation of products by its benzoate-oxiding enzyme system that are not acted upon by the catechol-metabolizing enzymes of the bacterium.
Abstract
Twenty isolates representing nine bacterial genera were obtained from enrichment cultures and were shown to cometabolize one or more of 22 substituted benzoates. One of the isolates, an Arthrobacter sp., cometabolized m-chlorobenzoate to a product identified as 4-chlorocatechol by thin-layer chromatography and ultraviolet and infrared spectroscopy. The data indicate that cometabolism by the arthrobacter results from the formation of products by its benzoate-oxiding enzyme system that are not acted upon by the catechol-metabolizing enzymes of the bacterium.

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Isolation and characterization of a 3-chlorobenzoate degrading pseudomonad.

TL;DR: A pseudomonad has been isolated from sewage, which can utilize 3-chlorobenzoic acid as a sole carbon source and cells grown on benzoate show additional high activities for the turnover of 3- and 4-chlorocatechols and chloromuconic acids.
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Microbial co-metabolism and the degradation of organic compounds in nature.

TL;DR: A new look at co-metABOLISM as a BIOCHEMICAL TECHNIQUE and its role in natural selection and human evolution.
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Microbial breakdown of halogenated aromatic pesticides and related compounds

TL;DR: This review will focus on the biodegradation and biotransformation pathways that have been established for halogenated phenols, phenoxyalkanoic acids, benzoic acid, benzenes, anilines and structurally related halogenation aromatic pesticides.
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Suicide Inactivation of Catechol 2,3-Dioxygenase from Pseudomonas putida mt-2 by 3-Halocatechols

TL;DR: Rates of inactivation by 3-fluorocatechol were reduced in the presence of superoxide dismutase, catalase, formate, and mannitol, which implies that superoxide anion, hydrogen peroxide, and hydroxyl radical exhibit additional inactivation.
Journal ArticleDOI

Degradation of polychlorinated biphenyls by two species of Achromobacter.

TL;DR: Benzoic and p-chlorobenzoic acids were produced from the degradation of BP and p CB, respectively, by Achromobacter pCB, indicating divergent degradation pathways.
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