Carbohydrate-aromatic interface and molecular architecture of lignocellulose

被引:129
|
作者
Kirui, Alex [1 ]
Zhao, Wancheng [1 ]
Deligey, Fabien [1 ]
Yang, Hui [2 ]
Kang, Xue [1 ,4 ]
Mentink-Vigier, Frederic [3 ]
Wang, Tuo [1 ]
机构
[1] Louisiana State Univ, Dept Chem, Baton Rouge, LA 70803 USA
[2] Penn State Univ, Dept Biol, University Pk, PA 16802 USA
[3] Natl High Magnet Field Lab, Tallahassee, FL 32310 USA
[4] Ningbo Univ, Inst Drug Discovery Technol, Ningbo 315211, Zhejiang, Peoples R China
基金
美国国家科学基金会;
关键词
SOLID-STATE NMR; DYNAMIC NUCLEAR-POLARIZATION; PLANT-CELL WALLS; LIGNIN-CARBOHYDRATE; BIOMASS RECALCITRANCE; ARABIDOPSIS-THALIANA; MAGNETIC-RESONANCE; MAIZE WALLS; CELLULOSE; PRETREATMENT;
D O I
10.1038/s41467-022-28165-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The plant biomass is a composite formed by a variety of polysaccharides and an aromatic polymer named lignin. Here, the authors use solid-state NMR spectroscopy to unveil the carbohydrate-aromatic interface that leads to the variable architecture of lignocellulose biomaterials. Plant cell walls constitute the majority of lignocellulosic biomass and serve as a renewable resource of biomaterials and biofuel. Extensive interactions between polysaccharides and the aromatic polymer lignin make lignocellulose recalcitrant to enzymatic hydrolysis, but this polymer network remains poorly understood. Here we interrogate the nanoscale assembly of lignocellulosic components in plant stems using solid-state nuclear magnetic resonance and dynamic nuclear polarization approaches. We show that the extent of glycan-aromatic association increases sequentially across grasses, hardwoods, and softwoods. Lignin principally packs with the xylan in a non-flat conformation via non-covalent interactions and partially binds the junction of flat-ribbon xylan and cellulose surface as a secondary site. All molecules are homogeneously mixed in softwoods; this unique feature enables water retention even around the hydrophobic aromatics. These findings unveil the principles of polymer interactions underlying the heterogeneous architecture of lignocellulose, which may guide the rational design of more digestible plants and more efficient biomass-conversion pathways.
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页数:12
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