拉曼光谱
显微镜
自体荧光
双光子激发显微术
拉曼散射
化学
拉曼显微镜
二次谐波产生
高光谱成像
生物物理学
细胞壁
化学成像
材料科学
荧光
光学
激光器
生物
物理
遥感
地质学
生物化学
作者
Zsuzsanna Heiner,Ingrid Zeise,Rivka Elbaum,Janina Kneipp
标识
DOI:10.1002/jbio.201700164
摘要
Spontaneous Raman scattering microspectroscopy, second harmonic generation (SHG) and 2‐photon excited fluorescence (2PF) were used in combination to characterize the morphology together with the chemical composition of the cell wall in native plant tissues. As the data obtained with unstained sections of Sorghum bicolor root and leaf tissues illustrate, nonresonant as well as pre‐resonant Raman microscopy in combination with hyperspectral analysis reveals details about the distribution and composition of the major cell wall constituents. Multivariate analysis of the Raman data allows separation of different tissue regions, specifically the endodermis, xylem and lumen. The orientation of cellulose microfibrils is obtained from polarization‐resolved SHG signals. Furthermore, 2‐photon autofluorescence images can be used to image lignification. The combined compositional, morphological and orientational information in the proposed coupling of SHG, Raman imaging and 2PF presents an extension of existing vibrational microspectroscopic imaging and multiphoton microscopic approaches not only for plant tissues.
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