Multi-scale visualization and characterization of lignocellulosic plant cell wall deconstruction during thermochemical pretreatment

被引:397
作者
Chundawat, Shishir P. S. [1 ,2 ]
Donohoe, Bryon S. [3 ]
Sousa, Leonardo da Costa [1 ]
Elder, Thomas [4 ]
Agarwal, Umesh P. [5 ]
Lu, Fachuang [2 ,6 ]
Ralph, John [2 ,6 ]
Himmel, Michael E. [3 ]
Balan, Venkatesh [1 ,2 ]
Dale, Bruce E. [1 ,2 ]
机构
[1] Michigan State Univ, BCRL, Lansing, MI 48910 USA
[2] US DOE, GLBRC, Washington, DC 20585 USA
[3] Natl Renewable Energy Lab, Biosci Ctr, Golden, CO 80401 USA
[4] USDA Forest Serv, So Res Stn, Pineville, LA 71360 USA
[5] USDA Forest Serv, Forest Prod Lab, Madison, WI 53726 USA
[6] Univ Wisconsin, Dept Biochem, Madison, WI 53726 USA
关键词
FIBER EXPANSION AFEX; ENZYMATIC-HYDROLYSIS; CORN STOVER; SECONDARY WALL; LIGNIN; CELLULOSE; ETHANOL; DELIGNIFICATION; OPTIMIZATION; MICROFIBRIL;
D O I
10.1039/c0ee00574f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Deconstruction of lignocellulosic plant cell walls to fermentable sugars by thermochemical and/or biological means is impeded by several poorly understood ultrastructural and chemical barriers. A promising thermochemical pretreatment called ammonia fiber expansion (AFEX) overcomes the native recalcitrance of cell walls through subtle morphological and physicochemical changes that enhance cellulase accessibility without extracting lignin and hemicelluloses into separate liquid streams. Multi-scale visualization and characterization of Zea mays (i.e., corn stover) cell walls were carried out by laser scanning confocal fluorescence microscopy (LSCM), Raman spectroscopy, atomic force microscopy (AFM), electron microscopy (SEM, TEM), nuclear magnetic resonance (NMR), and electron spectroscopy for chemical analysis (ESCA) to elucidate the mechanism of AFEX pretreatment. AFEX first dissolves, then extracts and, as the ammonia evaporates, redeposits cell wall decomposition products (e. g., amides, arabinoxylan oligomers, lignin-based phenolics) on outer cell wall surfaces. As a result, nanoporous tunnel-like networks, as visualized by 3D-electron tomography, are formed within the cell walls. We propose that this highly porous structure greatly enhances enzyme accessibility to embedded cellulosic microfibrils. The shape, size (10 to 1000 nm), and spatial distribution of the pores depended on their location within the cell wall and the pretreatment conditions used. Exposed pore surface area per unit AFEX pretreated cell wall volume, estimated via TEM-tomogram image analysis, ranged between 0.005 and 0.05 nm(2) per nm(3). AFEX results in ultrastructural and physicochemical modifications within the cell wall that enhance enzymatic hydrolysis yield by 4-5 fold over that of untreated cell walls.
引用
收藏
页码:973 / 984
页数:12
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