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. 1971 May;122(4):533–542. doi: 10.1042/bj1220533

Metabolism of 4-chloro-2-methylphenoxyacetate by a soil pseudomonad. Ring-fission, lactonizing and delactonizing enzymes

J K Gaunt 1, W C Evans 1
PMCID: PMC1176811  PMID: 5123887

Abstract

1. A cell-free system, prepared from Pseudomonas N.C.I.B. 9340 grown on 4-chloro-2-methylphenoxyacetate (MCPA) was shown to catalyse the reaction sequence: 5-chloro-3-methylcatechol → ciscis-γ-chloro-α-methylmuconate → γ-carboxymethylene-α-methyl-Δαβ-butenolide → γ-hydroxy-α-methylmuconate. 2. The activity of the three enzymes involved in these reactions was completely resolved and the lactonizing and delactonizing enzymes were separated. 3. This part of the metabolic pathway of 4-chloro-2-methylphenoxyacetate is thus confirmed for this bacterium. 4. The ring-fission oxygenase required Fe2+ or Fe3+ and reduced glutathione for activity; the lactonizing enzyme is stimulated by Mn2+, Mg2+, Co2+ and Fe2+; no cofactor requirement could be demonstrated for the delactonizing enzyme. 5. ciscis-γ-Chloro-α-methylmuconic acid was isolated and found to be somewhat unstable, readily lactonizing to γ-carboxymethylene-α-methyl-Δαβ-butenolide. 6. Enzymically the lactonization appears to be a single-step dehydrochlorinase reaction.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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