Gierlinger Notburga, Schwanninger Manfred
Max-Planck-Institute of Colloids and Interfaces, Department of Biomaterials, 14424 Potsdam, Germany.
Plant Physiol. 2006 Apr;140(4):1246-54. doi: 10.1104/pp.105.066993. Epub 2006 Feb 17.
Confocal Raman microscopy was used to illustrate changes of molecular composition in secondary plant cell wall tissues of poplar (Populus nigra x Populus deltoids) wood. Two-dimensional spectral maps were acquired and chemical images calculated by integrating the intensity of characteristic spectral bands. This enabled direct visualization of the spatial variation of the lignin content without any chemical treatment or staining of the cell wall. A small (0.5 microm) lignified border toward the lumen was observed in the gelatinous layer of poplar tension wood. The variable orientation of the cellulose was also characterized, leading to visualization of the S1 layer with dimensions smaller than 0.5 mum. Scanning Raman microscopy was thus shown to be a powerful, nondestructive tool for imaging changes in molecular cell wall organization with high spatial resolution.
共聚焦拉曼显微镜用于阐明杨树(黑杨×美洲黑杨)木材次生植物细胞壁组织中分子组成的变化。获取了二维光谱图,并通过对特征光谱带的强度进行积分来计算化学图像。这使得无需对细胞壁进行任何化学处理或染色就能直接观察木质素含量的空间变化。在杨树张力木的凝胶层中观察到朝向细胞腔的一个小的(0.5微米)木质化边界。还对纤维素的可变取向进行了表征,从而实现了尺寸小于0.5微米的S1层的可视化。因此,扫描拉曼显微镜被证明是一种强大的、非破坏性的工具,可用于以高空间分辨率对分子细胞壁组织的变化进行成像。