Metabolism of 2,5-dichlorobenzoic acid inPseudomonas stutzeri

Autor:	F. Kunc, S. A. Kozlovsky, G. M. Zaitsev
Rok vydání:	1994
Předmět:	Chlorobenzoates biology Chemistry Stereochemistry General Medicine Metabolism biology.organism_classification Microbiology Pseudomonas stutzeri Metabolic pathway chemistry.chemical_compound Stereospecificity Biochemistry Pseudomonadales Gentisic acid Pseudomonadaceae
Zdroj:	Folia Microbiologica. 39:399-403
ISSN:	1874-9356 0015-5632
DOI:	10.1007/bf02814446
Popis:	4-Chroropyrocatechol is formed as a results of the oxidation of 2,5-dichlorobenzoate byPseudomonas stutzeri. 3-Chloro-cis,cis-muconic acid is the product of the oxidation of 4-chloropyrocatechol. Pyrocatechol 1,2-dioxygenase, gentisate 1,2-dioxygenase, but not pyrocatechol 2,3-dioxygenase or protocatechuate 3,4-dioxygenase activities were found in cell-free extracts. Theortho cleavage activity for catechols appeared to involve induction of isoenzymes with different stereospecificity towards chlorocatechols. A catablic pathway for the degradation of 2,5-dichlorobenzoate by a newly isolated strain ofP. stutzeri was proposed.
Databáze:	OpenAIRE
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