Cellobiose dehydrogenase (CDH) gene transcripts were quantified by reverse transcription-PCR (RT-PCR) in cultures ofPhanerochaete chrysosporium supplemented with various cello-and xylooligosaccharides in order to elucidate the mechanism of enhanced CDH production in xylan/cellulose culture. Cellotriose and cellotetraose induced cdh expression, while xylobiose and xylotriose induced expression of cellobiohydrolase genes, especially cel7C.
The basidiomycete Phanerochaete chrysosporium produces various extracellular carbohydrate-degrading enzymes (14,24) and oxidative enzymes (13) that degrade wood, which contains cellulose, hemicellulose, and lignin as major components. Cellulose is a -1,4-linked homopolymer of glucose, and the cellulolytic system of this fungus involves multiple endoglucanases (EGs) and cellobiohydrolases (CBHs) (20, 21), which hydrolyze cellulose into cellobiose and cellooligosaccharides. In addition to hydrolytic enzymes, redox enzymes such as cellobiose dehydrogenase (CDH) are involved in cellulose degradation (1,3,4,23). CDH oxidizes cellobiose and cellooligosaccharides into the corresponding 1,5-␦-lactones (5, 15). The role of CDH in cellulose degradation has been widely discussed (7,8,10,25), and its relationship with polysaccharides monooxygenase was recently pointed out (12,16,22). A study by Dumonceaux and coworkers on a CDHdeficient mutant of the wood-rotting basidiomycete Trametes versicolor indicated that CDH is also involved in degradation of other plant cell wall components (2). We have recently reported that arabinoxylan, the major hemicellulose of monocots, enhances fungal growth and CDH production when it is supplemented into cellulose-degrading cultures, although it could not serve as a carbon source for P. chrysosporium by itself (6). In the present study, a similar response of the fungus was observed when glucuronoxylan (from beech wood) was added to cellulolytic culture, suggesting that the main-chain structure of xylan affects fungal growth, extracellular protein production and CDH activity. To elucidate the mechanism of these effects, we used reverse transcription-PCR (RT-PCR) to quantify CDH gene transcripts in cultures supplemented with xylose or xylooligosaccharides as well as glucose or cellooligosaccharides.Phanerochaete chrysosporium strain K-3 (9) was cultivated in Kremer and Wood medium (11) for 4 days with cellulose (CF11; Whatman, Fairfield, NJ), with or without xylan (from oat spelt, Serva Electrophoresis, Heidelberg, Germany; from beech, SigmaAldrich, St. Louis, MO). Briefly, xylan from beech wood has side chains of 4-O-methyl--D-glucuronic acid whereas that from oat spelt has additional side chains of ␣-L-arabinose. The packed volume of fungal mycelium and protein concentration of the culture filtrate were estimated as described previously (6). Cellobiose dehydrogenase (CDH) activity of the culture filtrates was assayed using cellobiose and cytochrome c as described previously (17). For transcriptional analysis in cultures with purified xylooligosac-