Abstract

In this study, chestnut shells (CNS), a recalcitrant and low-value agro-industrial waste obtained during the peeling of Castanea sativa fruits, were subjected to solid-state fermentation by six white-rot fungal strains (Irpex lacteus, Ganoderma resinaceum, Phlebia rufa, Bjerkandera adusta and two Trametes isolates). After being fermented, CNS was subjected to hydrolysis by a commercial enzymatic mix to evaluate the effect of fermentation in saccharification yield. After 48 h hydrolysis with 10 CMCase U mL−1 enzymatic mix, CNS fermented with both Trametes strains was recorded with higher saccharification yield (around 253 mg g−1 fermented CNS), representing 25% w/w increase in reducing sugars as compared to non-fermented controls. To clarify the relationships and general mechanisms of fungal fermentation and its impacts on substrate saccharification, the effects of some independent or explanatory variables in the production of reducing sugars were estimated by general predictive saccharification models. The variables considered were lignocellulolytic activities in fungal fermentation, CNS hydrolysis time, and concentration of enzymatic hydrolysis mix. Multiple linear regression analysis revealed a very high significant effect (p < 0.0001) of fungal laccase and xylanase activities in the saccharification models, thus proving the key potential of these enzymes in CNS solid-state fermentation.

Highlights

  • Lignocellulosic biomass from agricultural and forestry activities has been the object of increasing interest, due to decarbonization policies [1], as a renewable resource for the production of biofuels and value-added bioactive molecules [2,3,4,5,6]

  • white-rot fungi (WRF) mediated degradation of recalcitrant lignin of plant cell walls, involves oxidation reactions catalyzed by laccase, lignin peroxidase (LiP), manganese-dependent peroxidase (MnP) and versatile peroxidase (VP) enzymes

  • The highest values of reducing sugars production at 48 h hydrolysis occurred in samples fermented by Trametes strains

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Summary

Introduction

Lignocellulosic biomass from agricultural and forestry activities has been the object of increasing interest, due to decarbonization policies [1], as a renewable resource for the production of biofuels and value-added bioactive molecules [2,3,4,5,6]. In order to improve the access to structural polysaccharides of lignocellulosic biomass and their hydrolysis, the deconstruction of a complex cell wall matrix is an imperative operation. This step, which is one of the most expensive unit operations in the bioconversion process [9], should be selective, with minimum loss of carbohydrates and favoring lignin removal. This recalcitrant heteropolymer of plant cell wall, hinders

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