Direct fluorescence imaging of lignocellulosic and suberized cell walls in roots and stems
Investigating plant structure is fundamental in botanical science and provides crucial knowledge for the theories of plant evolution, ecophysiology and for the biotechnological practices. Modern plant anatomy often targets the formation, localization and characterization of cellulosic, lignified or...
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sg-ntu-dr.10356-1478892023-12-29T06:51:18Z Direct fluorescence imaging of lignocellulosic and suberized cell walls in roots and stems Kitin, Peter Nakaba, Satoshi Hunt, Christopher G. Lim, Sierin Funada, Ryo School of Chemical and Biomedical Engineering Engineering::Chemical engineering 3D Imaging Autofluorescence Investigating plant structure is fundamental in botanical science and provides crucial knowledge for the theories of plant evolution, ecophysiology and for the biotechnological practices. Modern plant anatomy often targets the formation, localization and characterization of cellulosic, lignified or suberized cell walls. While classical methods developed in the 1960s are still popular, recent innovations in tissue preparation, fluorescence staining and microscopy equipment offer advantages to the traditional practices for investigation of the complex lignocellulosic walls. Our goal is to enhance the productivity and quality of microscopy work by focusing on quick and cost-effective preparation of thick sections or plant specimen surfaces and efficient use of direct fluorescent stains. We discuss popular histochemical microscopy techniques for visualization of cell walls, such as autofluorescence or staining with calcofluor, Congo red (CR), fluorol yellow (FY) and safranin, and provide detailed descriptions of our own approaches and protocols. Autofluorescence of lignin in combination with CR and FY staining can clearly differentiate between lignified, suberized and unlignified cell walls in root and stem tissues. Glycerol can serve as an effective clearing medium as well as the carrier of FY for staining of suberin and lipids allowing for observation of thick histological preparations. Three-dimensional (3D) imaging of all cell types together with chemical information by wide-field fluorescence or confocal laser scanning microscopy (CLSM) was achieved. Published version 2021-04-14T06:12:37Z 2021-04-14T06:12:37Z 2020 Journal Article Kitin, P., Nakaba, S., Hunt, C. G., Lim, S. & Funada, R. (2020). Direct fluorescence imaging of lignocellulosic and suberized cell walls in roots and stems. AoB PLANTS, 12(4). https://dx.doi.org/10.1093/aobpla/plaa032 2041-2851 https://hdl.handle.net/10356/147889 10.1093/aobpla/plaa032 32793329 4 12 en AoB PLANTS © 2020 The Author(s). Published by Oxford University Press on behalf of the Annals of Botany Company. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. application/pdf |
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Engineering::Chemical engineering 3D Imaging Autofluorescence Kitin, Peter Nakaba, Satoshi Hunt, Christopher G. Lim, Sierin Funada, Ryo Direct fluorescence imaging of lignocellulosic and suberized cell walls in roots and stems |
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Investigating plant structure is fundamental in botanical science and provides crucial knowledge for the theories of plant evolution, ecophysiology and for the biotechnological practices. Modern plant anatomy often targets the formation, localization and characterization of cellulosic, lignified or suberized cell walls. While classical methods developed in the 1960s are still popular, recent innovations in tissue preparation, fluorescence staining and microscopy equipment offer advantages to the traditional practices for investigation of the complex lignocellulosic walls. Our goal is to enhance the productivity and quality of microscopy work by focusing on quick and cost-effective preparation of thick sections or plant specimen surfaces and efficient use of direct fluorescent stains. We discuss popular histochemical microscopy techniques for visualization of cell walls, such as autofluorescence or staining with calcofluor, Congo red (CR), fluorol yellow (FY) and safranin, and provide detailed descriptions of our own approaches and protocols. Autofluorescence of lignin in combination with CR and FY staining can clearly differentiate between lignified, suberized and unlignified cell walls in root and stem tissues. Glycerol can serve as an effective clearing medium as well as the carrier of FY for staining of suberin and lipids allowing for observation of thick histological preparations. Three-dimensional (3D) imaging of all cell types together with chemical information by wide-field fluorescence or confocal laser scanning microscopy (CLSM) was achieved. |
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School of Chemical and Biomedical Engineering |
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School of Chemical and Biomedical Engineering Kitin, Peter Nakaba, Satoshi Hunt, Christopher G. Lim, Sierin Funada, Ryo |
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Article |
author |
Kitin, Peter Nakaba, Satoshi Hunt, Christopher G. Lim, Sierin Funada, Ryo |
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Kitin, Peter |
title |
Direct fluorescence imaging of lignocellulosic and suberized cell walls in roots and stems |
title_short |
Direct fluorescence imaging of lignocellulosic and suberized cell walls in roots and stems |
title_full |
Direct fluorescence imaging of lignocellulosic and suberized cell walls in roots and stems |
title_fullStr |
Direct fluorescence imaging of lignocellulosic and suberized cell walls in roots and stems |
title_full_unstemmed |
Direct fluorescence imaging of lignocellulosic and suberized cell walls in roots and stems |
title_sort |
direct fluorescence imaging of lignocellulosic and suberized cell walls in roots and stems |
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2021 |
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https://hdl.handle.net/10356/147889 |
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