纤维素
生物量(生态学)
木质纤维素生物量
纤维素酶
化学
纤维素乙醇
水解
酶水解
催化作用
溶剂
糖
化学工程
有机化学
农学
生物
工程类
作者
Theodore W. Walker,Nathaniel Kuch,Kirk A. Vander Meulen,Catherine F. M. Clewett,George W. Huber,Brian G. Fox,James A. Dumesic
标识
DOI:10.1021/acssuschemeng.0c01538
摘要
Enzymes selectively hydrolyze the carbohydrate fractions of lignocellulosic biomass into corresponding sugars, but these processes are limited by low yields and slow catalytic turnovers. Under certain conditions, the rates and yields of enzymatic sugar production can be increased by pretreating biomass using solvents, heat and dilute acid catalysts. However, the mechanistic details underlying this behavior are not fully elucidated, and designing effective pretreatment strategies remains an empirical challenge. Herein, using a combination of solid-state and high-resolution magic-angle-spinning NMR, infrared spectroscopy and X-ray diffractometry, we show that the extent to which cellulase enzymes are able to hydrolyze solvent-pretreated biomass can be understood in terms of the ability of the solvent to break the chemical linkages between cellulose and non-cellulosic materials in the cell wall. This finding is of general significance to enzymatic biomass conversion research, and implications for designing improved biomass conversion strategies are discussed. These findings demonstrate the utility of solid-state NMR as a tool to elucidate the key chemical and physical changes that occur during the liquid-phase conversion of real biomass.
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