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Synergistic Carbocation Quenching and Bioprotective Shielding for Uncondensed Lignin and In Situ Saccharification

木质素 化学 水解 纤维素 有机化学 原位 化学工程 硫酸 生物净化 生物炼制 有机溶剂 溶剂 深共晶溶剂 支化(高分子化学) 单糖 纤维素酶 牙髓(牙) 三乙醇胺 亲核细胞 苯酚 乙醚 羟醛缩合 猝灭(荧光)
作者
Zhao Qin,Iqra Rustam,Jikai Zong,Ling Zhou,Xuyang Li,Junpeng Hu,Yan Zhang,Dachun Gong,Ge Hu,Dan Wang
出处
期刊:ACS Sustainable Chemistry & Engineering [American Chemical Society]
标识
DOI:10.1021/acssuschemeng.6c08548
摘要

Abstract The “lignin-first” biorefinery using deep eutectic solvents (DESs) offers a promising route to valorize lignocellulose, yet conventional acidic DESs suffer from severe lignin condensation and cellulase incompatibility, necessitating energy-intensive washing steps. Herein, we develop a multifunctional DES comprising choline prolinate ([Ch][Pro]) and gallic acid (GA) that enables one-pot biomass fractionation and in situ saccharification without any intermediate washing. Conductor-like screening model for real solvents (COSMO-RS) calculations guided the selection of [Ch][Pro] for its high lignin affinity. The [Ch][Pro]/GA DES operates through a synergistic three-layer protection mechanism. The nucleophilic –NH– group of prolinate quenches reactive Cα+ carbocations, preserving 91.0% uncondensed lignin with 82.3% β–O–4 linkages and only 8.4% condensation. GA's multiple phenolic hydroxyls cooperatively stabilize lignin via hydrogen bonding and π–π stacking, as evidenced by COSMO-RS thermodynamics (HE from –4.587 to –6.623 kJ·mol–1, lnγ from –2.586 to –4.974). Simultaneously, GA forms a dense hydrogen-bonding shield on cellulase, retaining 98.2% of the native α-helical conformation and 92.9% relative activity. Moreover, GA protects cellulose via a hydrogen-bond network, achieving >95% cellulose preservation. Consequently, a total reducing sugar yield of 90.2% is obtained after 24 h in situ enzymolysis at 50 °C, significantly outperforming conventional DES processes. The DES shows excellent recyclability, with optimized nanofiltration (150 Da + diafiltration) restoring delignification to 93.5% and enzyme compatibility to 91.8% after five cycles through effective removal of accumulated lignin fragments (94.8% removal), furfural/HMF (91.2% removal), and GA dimers (85.6% removal). This work establishes a rational multifunctional DES platform for lignin-first biorefining, combining high performance with economic and environmental sustainability, and provides a preliminary optimization framework for process scale-up.
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