
Chloroplasts are responsible for photosynthesis in plants and algae, and are composed of specific proteins and photosynthetic pigments, such as chlorophylls and carotenoids. When chlorophylls are exposed to adequate light, they emit a red autofluorescence. The quantity and quality of this autofluorescence are indicators of cell health and growth of the plant/alga; these indicators can also be used to determine biomass, agricultural yield, and environmental factors that affect plants/algae. Utilization of chlorophyll fluorescence to measure these parameters requires appropriate detection technologies, such as fluorescence imaging and spectrometric techniques. In addition to basic findings, these technologies contribute to research related to several global challenges, such as food security and environmental conservation. Furthermore, plants and algae produce carotenoids, which are high-value pigments used as additives in food, feed, and healthcare supplements. Similar to chlorophyll, several carotenoids emit clear fluorescence. Unfortunately, the predominant autofluorescence of their pigments occasionally becomes an encumbrance to observing other cellular molecules.
This Methods Collection invites articles on a variety of important and unique techniques for autofluorescence detection, imaging, and evaluation. Techniques to reduce interference from fluorescent pigments have important applications in evaluating other molecules. These technologies may contribute to the study of the above-mentioned global challenges and to the improvement of human health. Although the techniques in this collection would mostly focus on plants/algae, they may also involve other unique photosynthetic organisms such as symbiotic organisms (such as relationships between heterotrophic organisms and autotrophic algae). These symbiotic relationships play an important role in ecology and help us understand biological evolution.
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Cited by 2
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2021
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Yiwei Zhao1, Gene Chi Wai Man1,2, Loucia Kit Ying Chan1, Xi Guo1, Yingyu Liu3, Tao Zhang1, Joseph Kwong1,4, Chi Chiu Wang1,5, Xiaoyan Chen3, Tin Chiu Li1
1Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Prince of Wales Hospital, 2Department of Orthopaedics and Traumatology, The Chinese University of Hong Kong, Prince of Wales Hospital, 3Department of Obstetrics and Gynaecology, Shenzhen Baoan Women’s and Children’s Hospital, Shenzhen University, 4School of Medicine, Faculty of Medicine and Health Sciences, Keele University, 5Li Ka Shing Institute of Health Sciences; School of Biomedical Sciences, The Chinese University of Hong Kong
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Cited by 6
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2022
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Cited by 1
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2023
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1Microscopy Core Facility, Technological Research and Scientific Area (ACTI), University of Murcia, 2Confocal Microscopy and Cellular Imaging Unit, Genetic and Molecular Medicine Department, Pediatric Institute for Rare Diseases, Hospital Sant Joan de Déu, 3Research Institute Sant Joan de Déu, Esplugues de Llobregat, Spain 4Algology Laboratory, Biology Faculty, University of Murcia, 4Algology Laboratory, Biology Faculty, University of Murcia
A guide to deep UV quantitative phase and autofluorescence microscopy
Florian Ströhl*1
1UiT The Arctic University of Norway