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Volume 270, Number 49, Issue of December 8, 1995 pp. 29229-29235
©1995 by The American Society for Biochemistry and Molecular Biology, Inc.
From Xenobiotic to Antibiotic, Formation of Protoanemonin from 4-Chlorocatechol by Enzymes of the 3-Oxoadipate Pathway

(Received for publication, September 5, 1995; and in revised form, October 2, 1995)

Rafael Blasco Rolf-Michael Wittich Megharaj Mallavarapu Kenneth N. Timmis Dietmar H. Pieper

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.




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