Skip to main content
Fig. 5 | Biotechnology for Biofuels

Fig. 5

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

Fig. 5

H2O2 accumulation rate (a) and predicted “H2O2 consumption rate by LPMOs” (b) during enzymatic saccharification. Reactions containing 5% (w/v) Avicel were initially supplied with 1000 µM ascorbic acid and were run under anaerobic conditions with H2O2 feeding. Feed rates used: blue, 50 µmol h−1 H2O2; magenta, 100 µmol h−1 H2O2; red, 150 µmol h−1 H2O2. The rate of H2O2 accumulation was determined from a piecewise linear fit of the H2O2 concentration (in Fig. 2). The predicted H2O2 consumption rate by LPMOs was calculated as the difference of H2O2 feed rate and the sum of oxidation rate of AscA and accumulation rate of H2O2. 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

Back to article page