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Applied and Environmental Microbiology, June 2000, p. 2479-2483, Vol. 66, No. 6
UFZ Centre for Environmental Research
Leipzig-Halle, D-06120 Halle,1
Department of Cell and Molecular Biology,
Hans-Knöll-Institut für Naturstoff-Forschung e.V., D-07745
Jena,2 and Central
Research3 and Animal Health Research
and Development,4 Bayer AG, D-51368 Leverkusen,
Germany
Received 28 December 1999/Accepted 4 April 2000
While degrading 2,4-dichlorophenol, two strains of
Gloeophyllum striatum, a basidiomycetous fungus causing
brown rot decay of wood, simultaneously produced 4-chlorocatechol and
3,5-dichlorocatechol. These metabolites were identified by comparing
high-performance liquid chromatography retention times and mass
spectral data with those of chemically synthesized standards. Under
similar conditions, 3-hydroxyphthalic hydrazide was generated from
phthalic hydrazide, a reaction assumed to indicate hydroxyl radical
formation. Accordingly, during chemical degradation of
2,4-dichlorophenol by Fenton's reagent, identical metabolites were
formed. Both activities, the conversion of
2,4-[U-14C]dichlorophenol into
14CO2 and the generation of 3-hydroxyphthalic
hydrazide, were strongly inhibited by the hydroxyl radical scavenger
mannitol and in the absence of iron. These results provide new evidence
in favor of a Fenton-type degradation mechanism operative in
Gloeophyllum.
0099-2240/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Hydroxylated Metabolites of 2,4-Dichlorophenol
Imply a Fenton-Type Reaction in Gloeophyllum
striatum
*
Corresponding author. Mailing address: UFZ Centre for
Environmental Research Leipzig-Halle, Microbiology of Subterrestrial Aquatic Systems, Theodor-Lieser-Strasse 4, D-06120 Halle, Germany. Phone: 49 345 5585 204. Fax: 49 345 5585 559. E-mail:
schloss{at}hdg.ufz.de.
Dedicated to G. Gottschalk, University of Göttingen, on the
occasion of his 65th birthday.
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