From xenobiotic to antibiotic, formation of protoanemonin from 4-chlorocatechol by enzymes of the 3-oxoadipate pathway

J Biol Chem. 1995 Dec 8;270(49):29229-35. doi: 10.1074/jbc.270.49.29229.

Abstract

Chloroaromatics, a major class of industrial pollutants, may be oxidatively metabolized to chlorocatechols by soil and water microorganisms that have evolved catabolic activities toward these xenobiotics. We show here that 4-chlorocatechol can be further transformed by enzymes of the ubiquitous 3-oxoadipate pathway. However, whereas chloromuconate cycloisomerases catalyze the dechlorination of 3-chloro-cis,cis-muconate to form cis-dienelactone, muconate cycloisomerases catalyze a novel reaction, i.e. the dechlorination and concomitant decarboxylation to form 4-methylenebut-2-en-4-olide (protoanemonin), an ordinarily plant-derived antibiotic that is toxic to microorganisms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipates / metabolism*
  • Anti-Bacterial Agents / metabolism*
  • Catechols / metabolism*
  • Ecology
  • Furans / metabolism*
  • Intramolecular Lyases*
  • Isomerases / physiology
  • Pseudomonas / metabolism

Substances

  • Adipates
  • Anti-Bacterial Agents
  • Catechols
  • Furans
  • 3-oxoadipic acid
  • protoanemonin
  • Isomerases
  • Intramolecular Lyases
  • muconate cycloisomerase
  • 4-chlorocatechol