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Fig. 4 | Biotechnology for Biofuels

Fig. 4

From: In situ measurements of oxidation–reduction potential and hydrogen peroxide concentration as tools for revealing LPMO inactivation during enzymatic saccharification of cellulose

Fig. 4

Concentration (a) and calculated oxidation rate (b) of ascorbic acid during enzymatic saccharification of Avicel. Reactions were initially supplied with 1000 µM ascorbic acid and were run under anaerobic conditions with H2O2 feeding. Feed rates used: black symbols, no feeding of H2O2; blue, 50 µmol h−1 H2O2: magenta, 100 µmol h−1 H2O2: red, 150 µmol h−1 H2O2. The straight lines in panel (a) are trendlines obtained from fitting a kinetic model assuming a first-order reaction for the rate of ascorbic acid oxidation (see Materials and methods). The trendlines were used for calculation of oxidation rates in panel (b), using discrete steps of a few hours. The magenta and red arrows indicate the approximate time points where the rate of H2O2 accumulation in the medium started increasing for the reactions with 100 and 150 µmol h−1, respectively

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