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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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Copyright © 1995 by the American Society for Biochemistry and Molecular Biology.
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