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Citation
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HERO ID
7775314
Reference Type
Journal Article
Title
The meta cleavage of catechol by Azotobacter species. 4-Oxalocrotonate pathway
Author(s)
Sala-Trepat, JM; Evans, WC
Year
1971
Is Peer Reviewed?
Yes
Journal
European Journal of Biochemistry
ISSN:
0014-2956
EISSN:
1432-1033
Volume
20
Issue
3
Page Numbers
400-413
Language
English
PMID
4325686
DOI
10.1111/j.1432-1033.1971.tb01406.x
URL
https://www.scopus.com/inward/record.uri?eid=2-s2.0-0015219756&doi=10.1111%2fj.1432-1033.1971.tb01406.x&partnerID=40&md5=5613f0d94a41c6de8ee37825d9e999dc
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Abstract
Catechol was metabolized through 2‐hydroxymuconic semialdehyde by cell‐free extracts of benzoate‐grown Azotobacter Strains. Some properties of catechol 2,3 oxygenase preparations from Azotobacter vinelandii 206 are described. Two different enzymatic activities able to attack 2‐hydroxymuconic semialdehyde have been found in crude extracts from benzoate‐grown cells; one catalyses a hydrolytic release of formate from the semialdehyde and the other a dehydrogenation of this compound to 4‐oxalocrotonate. However, the low, non‐inducible levels of 2‐hydroxymuconic semialdehyde hydrolase activity appear negligible for metabolic purposes and the semialdehyde seems to be dissimilated almost exclusively via 4‐oxalocrotonate, by the action of a NAD+‐dependent dehydrogenase, in Azotobacter strains. A tautomerase activity responsible for the interconversion of the enol and keto forms of 4‐oxalocrotonic acid was found in extracts from benzoate‐grown cells. 4‐Oxalocrotonate was stoicheiometrically converted to CO2 and 4‐hydroxy‐2‐oxovalerate by a partially purified extract, with the transient formation of a compound that appears to be 2‐oxopent‐4‐enoic acid. The 4‐oxalocrotonate decarboxylase activity was stimulated by Mg2+ or Mn2+ ions and was inhibited by EDTA. Cell‐free extracts from Azotobacter strains converted synthetic 4‐hydroxy‐2‐oxovalerate to acetaldehyde and pyruvate. A reaction sequence, termed the 4‐oxalocrotonate pathway, for the dissimiation of catechol to acetaldehyde and pyruvate by Azotobacter species is presented. All the enzymes operative in this pathway were inducible, except the 4‐hydroxy‐2‐oxovalerate aldolase. The findings described here are discussed in connection with the two previously reported meta cleavage pathways for the oxidation of catechol in Pseudomonas strains. Copyright © 1971, Wiley Blackwell. All rights reserved
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