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Fig. 7 | Biotechnology for Biofuels

Fig. 7

From: Complete oxidation of hydroxymethylfurfural to furandicarboxylic acid by aryl-alcohol oxidase

Fig. 7

Comparison of the H2O2 equivalents detected (with AmplexRed/HRP) and the theoretical equivalents formed (according to the experimental conversion rates and the expected oxidase-type activity on all the substrates) in the reactions of HMF (a), DFF (b), and FFCA (c) with AAO in absence of catalase. Reactions between 1.5 mM substrate and 1.5 µM AAO were performed in 50 mM sodium phosphate, pH 6.0, at 28 °C

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