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Inhomogeneity of Cellulose Microfibril Assembly in Plant Cell Walls Revealed with Sum Frequency Generation Microscopy

The Journal of Physical Chemistry B · 26 Apr 2018 · 10.1021/acs.jpcb.8b01537

Abstract

Sum frequency generation (SFG) vibrational spectroscopy can selectively detect and analyze noncentrosymmetric components interspersed in amorphous matrices; this principle has been used for studies of nanoscale structure and mesoscale assembly of cellulose in plant cell walls. However, the spectral information averaged over a large area or volume cannot provide regiospecific or tissue-specific information of different cells in plants. This study demonstrates spatially resolved SFG analysis and imaging by combining a broad-band SFG spectroscopy system with an optical microscope. The system was designed to irradiate both narrow-band 800 nm and broad-band tunable IR beams through a single reflective objective lens, but from opposite sides of the surface normal direction of the sample. The developed technique was used to reveal inhomogeneous distributions of cellulose microfibrils within single cell walls, such as cotton fibers and onion epidermis as well as among different tissues in Arabidopsis inflorescence stems and bamboo culms. SFG microscopy can be used for vibrational spectroscopic imaging of other biological systems in complement to conventional Fourier transform infrared spectroscopy and confocal Raman microscopy.

Plant phenotyping relevance

植物細胞壁内のセルロース微小 fibril 分布という構造的植物形質を、空間分解SFG分光・顕微鏡で取得する手法を開発・実証しており、測定法が研究の中心である。

abstractThis study demonstrates spatially resolved SFG analysis and imaging by combining a broad-band SFG spectroscopy system with an optical microscope.
abstractThe developed technique was used to reveal inhomogeneous distributions of cellulose microfibrils within single cell walls

Code and data availability

The supplied blocks describe SFG microscopy measurements on cotton fibers, onion epidermis, Arabidopsis stems, and bamboo, but contain no public phenotype/trait dataset deposit, no author analysis code or workflow with an availability statement, and no trained models. The Supporting Information (raw spectra, intensity,

No evidence-backed public reproduction asset is currently recorded.

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