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Chemical structure and biodegradability of halogenated aromatic compounds. Conversion of chlorinated muconic acids into maleoylacetic acid

Authors :
Schmidt, E
Knackmuss, H J
Source :
Biochemical Journal; October 1980, Vol. 192 Issue: 1 p339-347, 9p
Publication Year :
1980

Abstract

1. An enzyme for the cycloisomerization of 2- and 3-chloro-cis, cis-muconic acid was isolated from 3-chlorobenzoate-grown cells of Pseudomonas sp. B13. It was named muconate cycloisomerase II, because it could it clearly be differentiated by its Km and Vmax. values from an ordinary muconate cycloisomerase, which functioned in benzoate catabolism and exhibited low activity with the chlorinated substrates. 2-Chloro-cis, cis-muconic acid was converted into trans- and 3-chloro-cis, cis–muconic acid into cis-4-carboxymethylenebut-2-en-4-olide together with dehalogenation. 2. An enzyme was isolated from chlorobenzoate-grown cells, which converted the 4-carboxymethylenebut-2-en-4-olides into maleoylacetic acid.

Details

Language :
English
ISSN :
02646021 and 14708728
Volume :
192
Issue :
1
Database :
Supplemental Index
Journal :
Biochemical Journal
Publication Type :
Periodical
Accession number :
ejs51293944
Full Text :
https://doi.org/10.1042/bj1920339