4.5 Article

Molecular and structural impacts of fungal depolymerization of corn stover to reduce pretreatment severity

期刊

SUSTAINABLE ENERGY & FUELS
卷 6, 期 23, 页码 5400-5413

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2se01091g

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  1. U.S. Department of Energy (DOE), Office of Energy Efficiency and Renewable Energy (EERE)
  2. Bioenergy Technologies Office (BETO) [DE-AC07-05ID14517]

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This study investigates the potential of using targeted pretreatments in the feedstock supply chain to enhance lignin degradation in lignocellulosic biomass. The results show that inoculating corn stover with lignin degrading fungi and storing it under simulated storage conditions can lead to degradation of hemicellulose and lignin, resulting in sugar degradation products. Lowering the reaction temperature in the pretreatment process can achieve equivalent xylose release in both stored and fungal treated samples.
The recalcitrance of lignocellulosic feedstocks to depolymerization is a significant barrier for renewable energy conversion approaches that require monomeric carbohydrates as inputs to conversion. This study assesses whether feedstock supply chain operations can be transformed into targeted pretreatments. Corn stover was inoculated with lignin degrading filamentous fungi (Phanerochaete chrysosporium), and then stored in aerated bioreactors designed to mimic storage conditions in large-scale storage piles to determine if fungal pretreatment enhanced lignin degradation. Composition changes resulting from P. chrysosporium treatment included hemicellulose and lignin degradation. Pyrolysis GCxGC/MS indicates that the cleavage of glycosidic bonds in hemicellulose resulted in sugar degradation products. Enhanced G and S lignol releases were observed. Dilute acid pretreatment and enzymatic hydrolysis indicated that lowering the reaction temperature to reduce pretreatment severity resulted in equivalent xylose release in unstored and fungal treated samples. These results suggest that this combined biological, thermochemical pretreatment can augment glycosidic bond cleavage and lignin degradation in lignocellulosic biorefineries.

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