The H2O2-dependent activity of a fungal lytic polysaccharide monooxygenase investigated with a turbidimetric assay

• Published in: Biotechnology for biofuels Vol. 13; no. 1; pp. 1 - 37
• Main Authors: Filandr, Frantisek, Man, Petr, Halada, Petr, Chang, Hucheng, Ludwig, Roland, Kracher, Daniel
• Format: Journal Article
• Language: English
• Published: London BioMed Central Ltd 05-03-2020; BioMed Central; BMC
• Subjects: Biochemical assays; Catalysis; Cellobiose dehydrogenase; Cellobiose dehydrogenase (acceptor); Cellulose; Enzymes; Experiments; Fungi; Glucose oxidase; Hydrogen peroxide; Kinetics; Light-scattering photometry; Lytic polysaccharide monooxygenase; Monooxygenase; Neurospora crassa; Observations; Optical properties; Oxidases; Oxidation-reduction reactions; Polysaccharides; Substrates (Biochemistry); Czech Republic
• ISSN: 1754-6834; 1754-6834
• DOI: 10.1186/s13068-020-01673-4

Abstract
Background
Lytic polysaccharide monooxygenases (LPMOs) are copper-dependent redox enzymes that cleave recalcitrant biopolymers such as cellulose, chitin, starch and hemicelluloses. Although LPMOs receive ample interest in industry and academia, their reaction mechanism is not yet fully understood. Recent studies showed that H
2
O
2
is a more efficient cosubstrate for the enzyme than O
2
, which could greatly affect the utilization of LPMOs in industrial settings.
Results
We probe the reactivity of LPMO9C from the cellulose-degrading fungus
Neurospora crassa
with a turbidimetric assay using phosphoric acid-swollen cellulose (PASC) as substrate and H
2
O
2
as a cosubstrate. The measurements were also followed by continuous electrochemical H
2
O
2
detection and LPMO reaction products were analysed by mass spectrometry. Different systems for the in situ generation of H
2
O
2
and for the reduction of LPMO’s active-site copper were employed, including glucose oxidase, cellobiose dehydrogenase, and the routinely used reductant ascorbate.
Conclusions
We found for all systems that the supply of H
2
O
2
limited LPMO’s cellulose depolymerization activity, which supports the function of H
2
O
2
as the relevant cosubstrate. The turbidimetric assay allowed rapid determination of LPMO activity on a cellulosic substrate without the need for time-consuming and instrumentally elaborate analysis methods.