@article{b741904ef3cc4491979a7b04cebb9277,
title = "Pontamine fast scarlet 4B bifluorescence and measurements of cellulose microfibril angles",
abstract = "Pontamine fast scarlet 4B is a red paper and textiles dye that has recently been introduced as a fluorescent probe for plant cell walls. Pontamine exhibits bifluorescence, or fluorescence dependent on the polarization of the excitation light: Because cellulose is aligned within the cell wall, pontamine-labelled cell walls exhibit variable fluorescence as the excitation polarization is modulated. Thus, bifluorescence measurements require polarized excitation that can be directly or indirectly modulated. In our confocal microscopy observations of various cellulose samples labelled with pontamine, we modulated excitation polarization either through sample rotation or by the confocal's scanfield rotation function. This variably rotated laser polarizations on Leica confocal microscopes, but not those from other makers. Beginning with samples with directly observable microfibril orientations, such as purified bacterial cellulose, the velamen of orchid roots and the inner S2 layer of radiata pine compression wood, we demonstrate that modelling the variations in pontamine fluorescence with a sine curve can be used to measure the known microfibril angles. We then measured average local microfibril angles in radiata pine samples, and showed similar microfibril angles in compression and normal (opposite) wood. Significantly, bifluorescence measurements might also be used to understand the degree of local cellulose alignment within the cell wall, as opposed to variations in the overall cellulose angle.",
keywords = "Bifluorescence, cellulose, microfibril angle, polarized light, pontamine fast scarlet 4B, radiata pine, secondary cell walls, velamen",
author = "J. Thomas and Idris, {N. A.} and Collings, {D. A.}",
note = "Funding Information: From the School of Biological Sciences at the University of Canterbury, we thank Alan Woods for the design and preparation of the rotatable microscope stage, Manfred Ingerfeld for assistance with confocal microscopy and Dave Conder for help with orchid culture. Stephen Thompson (Leica Microsystems, Australia) and Jacqui Ross (University of Auckland) provided helpful discussions. We also acknowledge the facilities and the scientific and technical assistance, of Ellie Kable and Gavin Tjin at the Australian Centre for Microscopy & Microanalysis at the University of Sydney, Vivian Rolland and Rosemary White at the Black Mountain Microimaging Centre (CSIRO Agriculture and Food, Canberra) and Louise Cole at the Advanced Microscopy Facility, Bosch Institute, University of Sydney. J.T. gratefully acknowledges the funding of his PhD scholarship that was generously provided by Scion while NAI acknowledges the Malaysian Education Ministry for her PhD scholarship (SLAB). Funding for this research was also provided by the School of Biological Sciences at the University of Canterbury, and by the Faculty of Science and Information Technology at the University of Newcastle. Funding Information: From the School of Biological Sciences at the University of Canterbury, we thank Alan Woods for the design and preparation of the rotatable microscope stage, Manfred Ingerfeld for assistance with confocal microscopy and Dave Conder for help with orchid culture. Stephen Thompson (Leica Microsystems, Australia) and Jacqui Ross (University of Auckland) provided helpful discussions. We also acknowledge the facilities and the scientific and technical assistance, of Ellie Kable and Gavin Tjin at the Australian Centre for Microscopy & Microanalysis at the University of Sydney, Vivian Rolland and Rosemary White at the Black Mountain Microimaging Centre (CSIRO Agriculture and Food, Canberra) and Louise Cole at the Advanced Microscopy Facility, Bosch Institute, University of Sydney. J.T. gratefully acknowledges the funding of his PhD scholarship Publisher Copyright: {\textcopyright} 2017 The Authors Journal of Microscopy {\textcopyright} 2017 Royal Microscopical Society",
year = "2017",
month = oct,
doi = "10.1111/jmi.12582",
language = "English",
volume = "268",
pages = "13--27",
journal = "Journal of Microscopy",
issn = "0022-2720",
publisher = "Wiley-Blackwell",
number = "1",
}