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本文引用的文献

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Tension wood as a model for functional genomics of wood formation.作为木材形成功能基因组学模型的张力木
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In-situ Raman microprobe studies of plant cell walls: Macromolecular organization and compositional variability in the secondary wall of Picea mariana (Mill.) B.S.P.原位拉曼微探针研究植物细胞壁:白云杉(Mill.)B.S.P.次生壁的大分子组织和组成变异性
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Fourier transform infrared microspectroscopy is a new way to look at plant cell walls.傅里叶变换红外显微镜光谱学是一种观察植物细胞壁的新方法。
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Lignification and tension wood.木质化与应力木
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Cellulose microfibril angle in the cell wall of wood fibres.木纤维细胞壁中的纤维素微纤丝角
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In situ Raman investigation of single lipid droplets in the water-conducting xylem of four woody plant species.四种木本植物物种导水木质部中单个脂滴的原位拉曼研究。
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Detection in situ and characterization of lignin in the G-layer of tension wood fibres of Populus deltoides.美洲黑杨张力木纤维G层中木质素的原位检测与表征
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FT-IR study of the Chara corallina cell wall under deformation.变形条件下轮藻细胞壁的傅里叶变换红外光谱研究
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利用共聚焦拉曼显微镜对杨树木细胞壁进行化学成像。

Chemical imaging of poplar wood cell walls by confocal Raman microscopy.

作者信息

Gierlinger Notburga, Schwanninger Manfred

机构信息

Max-Planck-Institute of Colloids and Interfaces, Department of Biomaterials, 14424 Potsdam, Germany.

出版信息

Plant Physiol. 2006 Apr;140(4):1246-54. doi: 10.1104/pp.105.066993. Epub 2006 Feb 17.

DOI:10.1104/pp.105.066993
PMID:16489138
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1435827/
Abstract

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.

摘要

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。