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Live-cell visualization of excitation energy dynamics in chloroplast thylakoid structures

The intricate molecular processes underlying photosynthesis have long been studied using various analytic approaches. However, the three-dimensional (3D) dynamics of such photosynthetic processes remain unexplored due to technological limitations related to investigating intraorganellar mechanisms i...

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Autores principales: Iwai, Masakazu, Yokono, Makio, Kurokawa, Kazuo, Ichihara, Akira, Nakano, Akihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4945916/
https://www.ncbi.nlm.nih.gov/pubmed/27416900
http://dx.doi.org/10.1038/srep29940
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author Iwai, Masakazu
Yokono, Makio
Kurokawa, Kazuo
Ichihara, Akira
Nakano, Akihiko
author_facet Iwai, Masakazu
Yokono, Makio
Kurokawa, Kazuo
Ichihara, Akira
Nakano, Akihiko
author_sort Iwai, Masakazu
collection PubMed
description The intricate molecular processes underlying photosynthesis have long been studied using various analytic approaches. However, the three-dimensional (3D) dynamics of such photosynthetic processes remain unexplored due to technological limitations related to investigating intraorganellar mechanisms in vivo. By developing a system for high-speed 3D laser scanning confocal microscopy combined with high-sensitivity multiple-channel detection, we visualized excitation energy dynamics in thylakoid structures within chloroplasts of live Physcomitrella patens cells. Two distinct thylakoid structures in the chloroplast, namely the grana and stroma lamellae, were visualized three-dimensionally in live cells. The simultaneous detection of the shorter (than ~670 nm) and longer (than ~680 nm) wavelength regions of chlorophyll (Chl) fluorescence reveals different spatial characteristics—irregular and vertical structures, respectively. Spectroscopic analyses showed that the shorter and longer wavelength regions of Chl fluorescence are affected more by free light-harvesting antenna proteins and photosystem II supercomplexes, respectively. The high-speed 3D time-lapse imaging of the shorter and longer wavelength regions also reveals different structural dynamics—rapid and slow movements within 1.5 seconds, respectively. Such structural dynamics of the two wavelength regions of Chl fluorescence would indicate excitation energy dynamics between light-harvesting antenna proteins and photosystems, reflecting the energetically active nature of photosynthetic proteins in thylakoid membranes.
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spelling pubmed-49459162016-07-26 Live-cell visualization of excitation energy dynamics in chloroplast thylakoid structures Iwai, Masakazu Yokono, Makio Kurokawa, Kazuo Ichihara, Akira Nakano, Akihiko Sci Rep Article The intricate molecular processes underlying photosynthesis have long been studied using various analytic approaches. However, the three-dimensional (3D) dynamics of such photosynthetic processes remain unexplored due to technological limitations related to investigating intraorganellar mechanisms in vivo. By developing a system for high-speed 3D laser scanning confocal microscopy combined with high-sensitivity multiple-channel detection, we visualized excitation energy dynamics in thylakoid structures within chloroplasts of live Physcomitrella patens cells. Two distinct thylakoid structures in the chloroplast, namely the grana and stroma lamellae, were visualized three-dimensionally in live cells. The simultaneous detection of the shorter (than ~670 nm) and longer (than ~680 nm) wavelength regions of chlorophyll (Chl) fluorescence reveals different spatial characteristics—irregular and vertical structures, respectively. Spectroscopic analyses showed that the shorter and longer wavelength regions of Chl fluorescence are affected more by free light-harvesting antenna proteins and photosystem II supercomplexes, respectively. The high-speed 3D time-lapse imaging of the shorter and longer wavelength regions also reveals different structural dynamics—rapid and slow movements within 1.5 seconds, respectively. Such structural dynamics of the two wavelength regions of Chl fluorescence would indicate excitation energy dynamics between light-harvesting antenna proteins and photosystems, reflecting the energetically active nature of photosynthetic proteins in thylakoid membranes. Nature Publishing Group 2016-07-15 /pmc/articles/PMC4945916/ /pubmed/27416900 http://dx.doi.org/10.1038/srep29940 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Iwai, Masakazu
Yokono, Makio
Kurokawa, Kazuo
Ichihara, Akira
Nakano, Akihiko
Live-cell visualization of excitation energy dynamics in chloroplast thylakoid structures
title Live-cell visualization of excitation energy dynamics in chloroplast thylakoid structures
title_full Live-cell visualization of excitation energy dynamics in chloroplast thylakoid structures
title_fullStr Live-cell visualization of excitation energy dynamics in chloroplast thylakoid structures
title_full_unstemmed Live-cell visualization of excitation energy dynamics in chloroplast thylakoid structures
title_short Live-cell visualization of excitation energy dynamics in chloroplast thylakoid structures
title_sort live-cell visualization of excitation energy dynamics in chloroplast thylakoid structures
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4945916/
https://www.ncbi.nlm.nih.gov/pubmed/27416900
http://dx.doi.org/10.1038/srep29940
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