Abstract
Cellobiose dehydrogenase activity (0.25–1 U Ml−1) is monitored by oxidation of cellobiose to cellobionolactone, thus reducing 2,6-dichlorophenolindophenol to a colourless compound. To prevent any β-glucosidase from reacting, gluconolactone is added as inhibitor. The sample throughput is 120 h−1.
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