Biodegradative mechanism of the brown rot Gloeophyllum trabeum: evidence for an extracellular fenton reaction
Kerem, Zohar; Jensen, Kenneth A.; Hammel, Kenneth E.
1999 FEBS Letters, Federation of European Biochemical Societies. 446: 49-54
Kerem, Zohar; Jensen, Kenneth A.; Hammel, Kenneth E., (1999), Biodegradative mechanism of the brown rot Gloeophyllum trabeum: evidence for an extracellular fenton reaction, FEBS Letters, Federation of European Biochemical Societies. 446: 49-54.
Abstract:
We have identified key components of the extra-cellular oxidative system that the brown rot fungus Gloeophyllum trabeum uses to degrade a recalcitrant polymer, polyethylene glycol, via hydrogen abstraction reactions. G. trabeum produced an extracellular metabolize, 2,5-dimethoxy-1,4-benzoquinone, and reduced it to 2,5-dimethoxyhydroquinone. In the presence of 2,5-dimethox-1,4-benzoquinone, the fungus also reduced extracellular Fe 3+ to Fe 2+ and produced extracelluar H2 O2 . Fe 3+ reduction and H2 O2 formation both resulted from a direct, non-enzymatic reaction between 2,5-dimethoxyhydroquinone and Fe 3+ .polyethylene glycol depolymerization by G. trabeum required both 2,5-dimethoxy-1,4-benzoquinone and Fe 3+ and was completely inhibited by catalase. These results provide evidence that G. trabeum uses a hydroquinone-driven Fenton reaction to cleave polyethylene glycol. We propose that similar reactions account for the ability of G. trabeum to attack lignocelluose.
Brown rot fungi are important contributors to the biomass recycling and soil fertility in forest ecosystems [1,2]. They also cause the most destructive type of decay in wooden structures [3]. These basidiomycetes are unusual in that they rapidly depolymerize the cellulose in wood without removing the sur-rounding lignin that normally prevents microbial attack. It is unlikely that the early steps in this process are enzymatic, because no known enzyme is small enough to penetrate sound wood [4]. Instead, brown rot fungi probably employ low mo-lecular weight (Mr ) degradative agents.