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Appl Environ Microbiol, June 1998, p. 2215-2219, Vol. 64, No. 6
Institut für Mikrobiologie und
Molekularbiologie,
Received 17 November 1997/Accepted 9 April 1998
We characterized the ability of a yeast to cleave the aromatic
structure of the dioxin-like compound dibenzofuran. The yeast strain
was isolated from a dioxin-contaminated soil sample and identified as
Trichosporon mucoides. During incubation of
glucose-pregrown cells with dibenzofuran, six major metabolites were
detected by high-performance liquid chromatography. The formation of
four different monohydroxylated dibenzofurans was proven by comparison of analytical data (gas chromatography-mass spectrometry) with that for
authentic standards. Further oxidation produced
2,3-dihydroxydibenzofuran and its ring cleavage product 2-(1-carboxy
methylidene)-2,3-dihydrobenzo[b]furanylidene glycolic
acid, which were characterized by mass spectrometry and 1H
nuclear magnetic resonance spectroscopy. These two metabolites are
derived from 2-hydroxydibenzofuran and 3-hydroxydibenzofuran, as shown
by incubation experiments using these monohydroxylated dibenzofurans as
substrates.
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Isolation and Characterization of a Dibenzofuran-Degrading Yeast:
Identification of Oxidation and Ring Cleavage Products
*
Corresponding author. Mailing address:
Ernst-Moritz-Arndt-Universität Greifswald, Institut für
Mikrobiologie und Molekularbiologie, F.-L.-Jahn-Str. 15, D-17487
Greifswald, Germany. Phone: 49-3834-864211. Fax: 49-3834-864202. E-mail: hammer{at}microbio1.biologie.uni-greifswald.de.
Appl Environ Microbiol, June 1998, p. 2215-2219, Vol. 64, No. 6
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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