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Applied and Environmental Microbiology, June 2001, p. 2705-2711, Vol. 67, No. 6
Institute for Microbial and Biochemical
Technology1 and Fiber Processing and
Paper Performance Research Work Unit,2 U.S.
Department of Agriculture Forest Products Laboratory, Madison,
Wisconsin 53705
Received 20 December 2000/Accepted 14 March 2001
The brown rot fungus Gloeophyllum trabeum uses an
extracellular hydroquinone-quinone redox cycle to reduce
Fe3+ and produce H2O2. These
reactions generate extracellular Fenton reagent, which enables
G. trabeum to degrade a wide variety of organic
compounds. We found that G. trabeum secreted two
quinones, 2,5-dimethoxy-1,4-benzoquinone (2,5-DMBQ) and
4,5-dimethoxy-1,2-benzoquinone (4,5-DMBQ), that underwent
iron-dependent redox cycling. Experiments that monitored the iron- and
quinone-dependent cleavage of polyethylene glycol by G.
trabeum showed that 2,5-DMBQ was more effective than 4,5-DMBQ
in supporting extracellular Fenton chemistry. Two factors contributed
to this result. First, G. trabeum reduced 2,5-DMBQ to
2,5-dimethoxyhydroquinone (2,5-DMHQ) much more rapidly than it reduced
4,5-DMBQ to 4,5-dimethoxycatechol (4,5-DMC). Second, although both
hydroquinones reduced ferric oxalate complexes, the predominant form of
Fe3+ in G. trabeum cultures, the
2,5-DMHQ-dependent reaction reduced O2 more rapidly than
the 4,5-DMC-dependent reaction. Nevertheless, both hydroquinones
probably contribute to the extracellular Fenton chemistry of G.
trabeum, because 2,5-DMHQ by itself is an efficient reductant
of 4,5-DMBQ.
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.6.2705-2711.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Pathways for Extracellular Fenton Chemistry in the
Brown Rot Basidiomycete Gloeophyllum trabeum
*
Corresponding author. Mailing address: Institute for
Microbial and Biochemical Technology, USDA Forest Products Laboratory, One Gifford Pinchot Dr., Madison, WI 53705. Phone: (608) 231-9528. Fax:
(608) 231-9262. E-mail: kehammel{at}facstaff.wisc.edu.
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