Production of H 2 O 2 in Phanerochaete chrysosporium during lignin degradation

Evidence in support of an essential role for H 2 O 2 in lignin degradation by the white-rot fungus Phanerochaete chrysosporium has been presented by several laboratories. H 2 O 2 is formed simultaneously with the ligninolytic system, and when it is degraded by catalase the lignin-degrading capacity is also reduced. We have now identified, purified and characterized a sugar-oxidizing enzyme that produces H 2 O 2 during glucose starvation in P. chrysosporium . The enzyme oxidizes glucose at the 2-carbon position to yield glucosone, but 5-n-gluconolactone and xylose are also oxidized at significant rates. Another H 2 O 2 -producing enzyme in P.chrysosporium , methanol oxidase, has also been identified, purified and characterized in this laboratory. Methanol is formed from the methoxyl groups in lignin. Hydrogen peroxide, necessary for further degradation of lignin, is formed by enzyme-catalysed oxidation of the lignin-derived methanol. Induction and repression of the H 2 O 2 -producing enzymes is discussed, as well as ways for the fungus to control the glucose level in its environment.

1979 ◽  
Vol 57 (19) ◽  
pp. 2050-2058 ◽  
Author(s):  
Ian D. Reid

The degradation by Phanerochaete chrysosporium of "natural" lignin in aspen wood, like synthetic lignin, was inhibited by nitrogen and stimulated by carbohydrate. Nitrogen delayed the appearance and reduced the level of ligninolytic activity and indirectly hastened its decline by accelerating depletion of the carbohydrate supply. The carbon:nitrogen ratio of the medium was a better predictor of lignin degradation than the absolute carbohydrate and nitrogen levels. Unlike nitrogen limitation, sulphate and phosphate limitation of growth did not stimulate lignin metabolism.


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