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Measuring the dynamic response of the thylakoid architecture in plant leaves by electron microscopy

The performance of the photosynthesis machinery in plants, including light harvesting, electron transport, and protein repair, is controlled by structural changes in the thylakoid membrane system inside the chloroplasts. In particular, the structure of the stacked grana area of thylakoid membranes i...

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Autores principales: Li, Meng, Mukhopadhyay, Roma, Svoboda, Václav, Oung, Hui Min Olivia, Mullendore, Daniel L., Kirchhoff, Helmut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644818/
https://www.ncbi.nlm.nih.gov/pubmed/33195966
http://dx.doi.org/10.1002/pld3.280
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author Li, Meng
Mukhopadhyay, Roma
Svoboda, Václav
Oung, Hui Min Olivia
Mullendore, Daniel L.
Kirchhoff, Helmut
author_facet Li, Meng
Mukhopadhyay, Roma
Svoboda, Václav
Oung, Hui Min Olivia
Mullendore, Daniel L.
Kirchhoff, Helmut
author_sort Li, Meng
collection PubMed
description The performance of the photosynthesis machinery in plants, including light harvesting, electron transport, and protein repair, is controlled by structural changes in the thylakoid membrane system inside the chloroplasts. In particular, the structure of the stacked grana area of thylakoid membranes is highly dynamic, changing in response to different environmental cues such as light intensity. For example, the aqueous thylakoid lumen enclosed by thylakoid membranes in grana has been documented to swell in the presence of light. However, light‐induced alteration of the stromal gap in the stacked grana (partition gap) and of the unstacked stroma lamellae has not been well characterized. Light‐induced changes in the entire thylakoid membrane system, including the lumen in both stacked and unstacked domains as well as the partition gap, are presented here, and the functional implications are discussed. This structural analysis was made possible by development of a robust semi‐automated image analysis method combined with optimized plant tissue fixation techniques for transmission electron microscopy generating quantitative structural results for the analysis of thylakoid ultrastructure. SIGNIFICANCE STATEMENT: A methodical pipeline ranging from optimized leaf tissue preparation for electron microscopy to quantitative image analysis was established. This methodical development was employed to study details of light‐induced changes in the plant thylakoid ultrastructure. It was found that the lumen of the entire thylakoid system (stacked and unstacked domains) undergoes light‐induced swelling, whereas adjacent membranes on the stroma side in stacked grana thylakoid approach each other.
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spelling pubmed-76448182020-11-13 Measuring the dynamic response of the thylakoid architecture in plant leaves by electron microscopy Li, Meng Mukhopadhyay, Roma Svoboda, Václav Oung, Hui Min Olivia Mullendore, Daniel L. Kirchhoff, Helmut Plant Direct Original Research The performance of the photosynthesis machinery in plants, including light harvesting, electron transport, and protein repair, is controlled by structural changes in the thylakoid membrane system inside the chloroplasts. In particular, the structure of the stacked grana area of thylakoid membranes is highly dynamic, changing in response to different environmental cues such as light intensity. For example, the aqueous thylakoid lumen enclosed by thylakoid membranes in grana has been documented to swell in the presence of light. However, light‐induced alteration of the stromal gap in the stacked grana (partition gap) and of the unstacked stroma lamellae has not been well characterized. Light‐induced changes in the entire thylakoid membrane system, including the lumen in both stacked and unstacked domains as well as the partition gap, are presented here, and the functional implications are discussed. This structural analysis was made possible by development of a robust semi‐automated image analysis method combined with optimized plant tissue fixation techniques for transmission electron microscopy generating quantitative structural results for the analysis of thylakoid ultrastructure. SIGNIFICANCE STATEMENT: A methodical pipeline ranging from optimized leaf tissue preparation for electron microscopy to quantitative image analysis was established. This methodical development was employed to study details of light‐induced changes in the plant thylakoid ultrastructure. It was found that the lumen of the entire thylakoid system (stacked and unstacked domains) undergoes light‐induced swelling, whereas adjacent membranes on the stroma side in stacked grana thylakoid approach each other. John Wiley and Sons Inc. 2020-11-05 /pmc/articles/PMC7644818/ /pubmed/33195966 http://dx.doi.org/10.1002/pld3.280 Text en © 2020 The Authors. Plant Direct published by American Society of Plant Biologists, Society for Experimental Biology and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Li, Meng
Mukhopadhyay, Roma
Svoboda, Václav
Oung, Hui Min Olivia
Mullendore, Daniel L.
Kirchhoff, Helmut
Measuring the dynamic response of the thylakoid architecture in plant leaves by electron microscopy
title Measuring the dynamic response of the thylakoid architecture in plant leaves by electron microscopy
title_full Measuring the dynamic response of the thylakoid architecture in plant leaves by electron microscopy
title_fullStr Measuring the dynamic response of the thylakoid architecture in plant leaves by electron microscopy
title_full_unstemmed Measuring the dynamic response of the thylakoid architecture in plant leaves by electron microscopy
title_short Measuring the dynamic response of the thylakoid architecture in plant leaves by electron microscopy
title_sort measuring the dynamic response of the thylakoid architecture in plant leaves by electron microscopy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644818/
https://www.ncbi.nlm.nih.gov/pubmed/33195966
http://dx.doi.org/10.1002/pld3.280
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