{"title":"深度共晶溶剂对缩合木质素的改性:洞察改善酶糖化的机理","authors":"Tingjun Chen, Xuelian Zhou, Yunni Zhan, Jinyuan Cheng, Caoxing Huang, Chang Geun Yoo, Guigan Fang, Arthur J. Ragauskas, Xianzhi Meng, Chen Huang","doi":"10.1021/acssuschemeng.4c05937","DOIUrl":null,"url":null,"abstract":"Liquid hot water pretreatment (LHWP) can convert hemicellulose in biomass into valuable xylooligosaccharides, but the utilization of glucan in the solid residue after hemicellulose extraction is usually constrained due to the significant lignin condensation during the LHWP. To alleviate lignin’s inhibition on glucan saccharification, this study established a variety of functional deep eutectic solvents (DESs) for the pretreatment of the solid residues after LHWP. The applied DES pretreatments resulted in different glucan saccharification yields. Under the premise of similar lignin removal, the ChCl/ethylene glycol (EG) system obtained near complete glucan digestibility, while the acid or alkali DESs had much lower enzymatic saccharification yields (35.7% and 20.6%). The mechanism of boosting the glucan saccharification by ChCl/EG was comprehensively analyzed by 2D-HSQC NMR, hydrophobicity, GPC and Langmuir adsorption isotherm of enzymes onto the cellulolytic enzyme lignin. Results indicated that lignin remaining in the ChCl/EG pretreated substrates had a lower hydrophobicity (2.8 L/g) and enzyme adsorption (4.6 mg/g), resulting from the EG grafting onto the α-position of the lignin side chain (as high as 5.0/100 Ar). The LHWP-DES pretreatment in this study unveiled the mechanism for cellulose digestibility enhancement using three common DESs and maximized the enzymatic hydrolysis yield, which provided a new scheme for the high-value utilization of biomass.","PeriodicalId":25,"journal":{"name":"ACS Sustainable Chemistry & Engineering","volume":"22 1","pages":""},"PeriodicalIF":7.1000,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Modification of Condensed Lignin by Deep Eutectic Solvents: Insight into the Mechanism of Improving the Enzymatic Saccharification\",\"authors\":\"Tingjun Chen, Xuelian Zhou, Yunni Zhan, Jinyuan Cheng, Caoxing Huang, Chang Geun Yoo, Guigan Fang, Arthur J. Ragauskas, Xianzhi Meng, Chen Huang\",\"doi\":\"10.1021/acssuschemeng.4c05937\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Liquid hot water pretreatment (LHWP) can convert hemicellulose in biomass into valuable xylooligosaccharides, but the utilization of glucan in the solid residue after hemicellulose extraction is usually constrained due to the significant lignin condensation during the LHWP. To alleviate lignin’s inhibition on glucan saccharification, this study established a variety of functional deep eutectic solvents (DESs) for the pretreatment of the solid residues after LHWP. The applied DES pretreatments resulted in different glucan saccharification yields. Under the premise of similar lignin removal, the ChCl/ethylene glycol (EG) system obtained near complete glucan digestibility, while the acid or alkali DESs had much lower enzymatic saccharification yields (35.7% and 20.6%). The mechanism of boosting the glucan saccharification by ChCl/EG was comprehensively analyzed by 2D-HSQC NMR, hydrophobicity, GPC and Langmuir adsorption isotherm of enzymes onto the cellulolytic enzyme lignin. Results indicated that lignin remaining in the ChCl/EG pretreated substrates had a lower hydrophobicity (2.8 L/g) and enzyme adsorption (4.6 mg/g), resulting from the EG grafting onto the α-position of the lignin side chain (as high as 5.0/100 Ar). 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引用次数: 0
摘要
液态热水预处理(LHWP)可将生物质中的半纤维素转化为有价值的木寡糖,但由于液态热水预处理过程中木质素的大量凝结,通常会限制半纤维素提取后固体残渣中葡聚糖的利用。为了缓解木质素对葡聚糖糖化的抑制作用,本研究建立了多种功能性深共晶溶剂(DES),用于 LHWP 后固体残渣的预处理。所采用的 DES 预处理方法导致了不同的葡聚糖糖化率。在木质素去除率相似的前提下,氯化氢/乙二醇(EG)体系可获得接近完全的葡聚糖消化率,而酸性或碱性 DES 的酶糖化率则低得多(35.7% 和 20.6%)。通过二维-HSQC NMR、疏水性、GPC 和酶对纤维素分解酶木质素的朗缪尔吸附等温线,全面分析了 ChCl/EG 促进葡聚糖糖化的机理。结果表明,ChCl/EG 预处理基质中残留的木质素具有较低的疏水性(2.8 L/g)和酶吸附性(4.6 mg/g),这是由于 EG 接枝到了木质素侧链的 α 位(高达 5.0/100 Ar)。本研究中的 LHWP-DES 预处理揭示了使用三种常见 DESs 提高纤维素消化率的机理,并最大限度地提高了酶水解产率,为生物质的高值化利用提供了一种新方案。
Modification of Condensed Lignin by Deep Eutectic Solvents: Insight into the Mechanism of Improving the Enzymatic Saccharification
Liquid hot water pretreatment (LHWP) can convert hemicellulose in biomass into valuable xylooligosaccharides, but the utilization of glucan in the solid residue after hemicellulose extraction is usually constrained due to the significant lignin condensation during the LHWP. To alleviate lignin’s inhibition on glucan saccharification, this study established a variety of functional deep eutectic solvents (DESs) for the pretreatment of the solid residues after LHWP. The applied DES pretreatments resulted in different glucan saccharification yields. Under the premise of similar lignin removal, the ChCl/ethylene glycol (EG) system obtained near complete glucan digestibility, while the acid or alkali DESs had much lower enzymatic saccharification yields (35.7% and 20.6%). The mechanism of boosting the glucan saccharification by ChCl/EG was comprehensively analyzed by 2D-HSQC NMR, hydrophobicity, GPC and Langmuir adsorption isotherm of enzymes onto the cellulolytic enzyme lignin. Results indicated that lignin remaining in the ChCl/EG pretreated substrates had a lower hydrophobicity (2.8 L/g) and enzyme adsorption (4.6 mg/g), resulting from the EG grafting onto the α-position of the lignin side chain (as high as 5.0/100 Ar). The LHWP-DES pretreatment in this study unveiled the mechanism for cellulose digestibility enhancement using three common DESs and maximized the enzymatic hydrolysis yield, which provided a new scheme for the high-value utilization of biomass.
期刊介绍:
ACS Sustainable Chemistry & Engineering is a prestigious weekly peer-reviewed scientific journal published by the American Chemical Society. Dedicated to advancing the principles of green chemistry and green engineering, it covers a wide array of research topics including green chemistry, green engineering, biomass, alternative energy, and life cycle assessment.
The journal welcomes submissions in various formats, including Letters, Articles, Features, and Perspectives (Reviews), that address the challenges of sustainability in the chemical enterprise and contribute to the advancement of sustainable practices. Join us in shaping the future of sustainable chemistry and engineering.