Davies Lynette M, Harris Philip J, Newman Roger H
School of Biological Sciences, The University of Auckland, Private Bag 92019, Auckland, New Zealand.
Carbohydr Res. 2002 Apr 2;337(7):587-93. doi: 10.1016/s0008-6215(02)00038-1.
Solid-state CP/MAS 13C NMR spectroscopy was used to determine the effects of three different sequential extraction procedures, used to remove non-cellulosic polysaccharides, on the molecular ordering of cellulose in a cell-wall preparation containing mostly primary cell walls obtained from the leaves of the model dicotyledon, Arabidopsis thaliana. The extractions were 50 mM trans-1,2-diaminocyclohexane N,N,N',N'-tetraacetic acid (CDTA) and 50 mM sodium carbonate (giving Residue 1); 50 mM CDTA, 50 mM sodium carbonate and 1 M KOH (giving Residue 2); and 50 mM CDTA, 50 mM sodium carbonate and 4 M KOH (giving Residue 3). The molecular ordering of cellulose in Residue 1 was similar to that in unextracted walls: the cellulose was almost all crystalline, with 43% of molecules contained in crystallite interiors and similar proportions of the triclinic (I(alpha)) and monoclinic (I(beta)) crystal forms. Residue 2 was partly decrystallized and the remaining crystallites were mostly in the I(beta) form. Residue 3 was a mixture of cellulose II, cellulose I and amorphous cellulose. The presence of signals at 100.0 and 102.3 ppm in the spectra of Residues 1 and 2, but not of unextracted cell walls, suggested that the extractions giving these residues caused some of the non-cellulosic polysaccharides, possibly xyloglucans and galactoglucomannans, to become relatively well ordered, for example through interactions with cellulose crystallite surfaces.
采用固态交叉极化/魔角旋转(CP/MAS)13C核磁共振光谱法,来确定三种不同的顺序提取程序对纤维素分子排列的影响。这三种提取程序用于去除非纤维素多糖,样本是一种细胞壁制剂,主要包含从模式双子叶植物拟南芥叶片中获得的初生细胞壁。提取过程如下:50 mM反式-1,2-二氨基环己烷N,N,N',N'-四乙酸(CDTA)和50 mM碳酸钠(得到残渣1);50 mM CDTA、50 mM碳酸钠和1 M氢氧化钾(得到残渣2);50 mM CDTA、50 mM碳酸钠和4 M氢氧化钾(得到残渣3)。残渣1中纤维素的分子排列与未提取细胞壁中的相似:纤维素几乎全部为结晶态,微晶内部包含43%的分子,三斜晶型(I(α))和单斜晶型(I(β))的比例相似。残渣2部分脱结晶,剩余的微晶大多为I(β)型。残渣3是纤维素II、纤维素I和无定形纤维素的混合物。残渣1和2的光谱中在100.0和102.3 ppm处有信号,而未提取的细胞壁光谱中没有,这表明产生这些残渣的提取过程使一些非纤维素多糖,可能是木葡聚糖和半乳葡甘露聚糖,通过与纤维素微晶表面的相互作用而变得相对有序。