Abstract

BackgroundThe discovery of enzymes named lytic polysaccharide monooxygenases (LPMOs) has had a major impact on the efficiency of current commercial cellulase cocktails for saccharification of lignocellulosic biomass. However, the notion that LPMOs use molecular oxygen as a co-substrate and require two externally delivered electrons per catalytic cycle poses a challenge in the development of efficient large-scale industrial processes. Building on the recent discovery that H2O2, rather than O2, is the co-substrate of LPMOs, we show here how cellulose degradation by the LPMO-containing commercial cellulase cocktail Cellic® CTec2 can be controlled and boosted by supplying the reaction with H2O2.ResultsThe controlled supply of anaerobic hydrolysis reactions with H2O2 and sub-stoichiometric amounts of reductant increased apparent LPMO activity by almost two orders of magnitude compared to standard aerobic reactions utilizing O2 and stoichiometric amounts of reductant. Improved LPMO activity was correlated with enhanced saccharification rates and yields for a model cellulosic substrate (Avicel) as well as industrial lignocellulosic substrates (sulfite-pulped Norway spruce and steam-exploded birch), although the magnitude of the effects was substrate dependent. Improvements in lignocellulose conversions were achieved at low H2O2 feeding rates (in the range of 90–600 µM h−1). Tight control of LPMO reactions by controlled supply of H2O2 under anaerobic conditions was possible.ConclusionWe report saccharification rates and yields for a model substrate (Avicel) and industrial lignocellulosic substrates that, at low H2O2 feeding rates, are higher than those seen under standard aerobic conditions. In an industrial setting, controlling and supplying molecular oxygen and stoichiometric amounts of reductant are challenging. The present report shows that the use of small amounts of a liquid bulk chemical, H2O2, provides an alternative to the currently available processes, which likely is cheaper and more easy to control, while giving higher product yields.

Highlights

  • The discovery of enzymes named lytic polysaccharide monooxygenases (LPMOs) has had a major impact on the efficiency of current commercial cellulase cocktails for saccharification of lignocellulosic biomass

  • Roles of LPMOs in lignocellulose degradation The results presented above show that LPMO activity can be controlled and boosted by regulating the supply of ­H2O2, and show the complex interplay between many factors including undesirable side reactions involving ­H2O2

  • The present study shows that the power of LPMOs in modern cellulolytic cocktails can be controlled and harnessed by controlling ­H2O2 supply

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Summary

Introduction

The discovery of enzymes named lytic polysaccharide monooxygenases (LPMOs) has had a major impact on the efficiency of current commercial cellulase cocktails for saccharification of lignocellulosic biomass. LPMOs, whose activity was discovered in 2010 [5], are mono-copper redox enzymes [6, 7] that catalyze the hydroxylation of C1 and/or C4 carbons involved in the glycosidic bonds that connect the glucose units in cellulose [6,7,8] This hydroxylation leads to destabilization and cleavage of glycosidic bonds [9], disturbing the crystalline structure of the cellulose [10], and offering access points for canonical cellulases that can further process the recalcitrant polysaccharide [11,12,13]. This is well illustrated by the positive effect of LPMOs on biomass conversion efficiency [5, 14,15,16]

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