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The reactions were performed by incubating 0µM (for the control) or 0.2 µM of each enzyme with 2.5 mg ml-1 of cellotetraose (G4) or cellopentaose (G5) in a citrate buffer (pH 6.0) at 75°C for 24 h. Samples were taken at different time points and analyzed using an HPLC method.
