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Development of fluorescence quenching in Chlamydomonas reinhardtii upon prolonged illumination at 77 K
Low-temperature fluorescence measurements are frequently used in photosynthesis research to assess photosynthetic processes. Upon illumination of photosystem II (PSII) frozen to 77 K, fluorescence quenching is observed. In this work, we studied the light-induced quenching in intact cells of Chlamydo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182390/ https://www.ncbi.nlm.nih.gov/pubmed/29948747 http://dx.doi.org/10.1007/s11120-018-0534-8 |
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author | Wlodarczyk, Lucyna M. Snellenburg, Joris J. Dekker, Jan P. Stokkum, Ivo H. M. |
author_facet | Wlodarczyk, Lucyna M. Snellenburg, Joris J. Dekker, Jan P. Stokkum, Ivo H. M. |
author_sort | Wlodarczyk, Lucyna M. |
collection | PubMed |
description | Low-temperature fluorescence measurements are frequently used in photosynthesis research to assess photosynthetic processes. Upon illumination of photosystem II (PSII) frozen to 77 K, fluorescence quenching is observed. In this work, we studied the light-induced quenching in intact cells of Chlamydomonas reinhardtii at 77 K using time-resolved fluorescence spectroscopy with a streak camera setup. In agreement with previous studies, global analysis of the data shows that prolonged illumination of the sample affects the nanosecond decay component of the PSII emission. Using target analysis, we resolved the quenching on the PSII-684 compartment which describes bulk chlorophyll molecules of the PSII core antenna. Further, we quantified the quenching rate constant and observed that as the illumination proceeds the accumulation of the quencher leads to a speed up of the fluorescence decay of the PSII-684 compartment as the decay rate constant increases from about 3 to 4 ns(− 1). The quenching on PSII-684 leads to indirect quenching of the compartments PSII-690 and PSII-695 which represent the red chlorophyll of the PSII core. These results explain past and current observations of light-induced quenching in 77 K steady-state and time-resolved fluorescence spectra. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11120-018-0534-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6182390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-61823902018-10-22 Development of fluorescence quenching in Chlamydomonas reinhardtii upon prolonged illumination at 77 K Wlodarczyk, Lucyna M. Snellenburg, Joris J. Dekker, Jan P. Stokkum, Ivo H. M. Photosynth Res Original Article Low-temperature fluorescence measurements are frequently used in photosynthesis research to assess photosynthetic processes. Upon illumination of photosystem II (PSII) frozen to 77 K, fluorescence quenching is observed. In this work, we studied the light-induced quenching in intact cells of Chlamydomonas reinhardtii at 77 K using time-resolved fluorescence spectroscopy with a streak camera setup. In agreement with previous studies, global analysis of the data shows that prolonged illumination of the sample affects the nanosecond decay component of the PSII emission. Using target analysis, we resolved the quenching on the PSII-684 compartment which describes bulk chlorophyll molecules of the PSII core antenna. Further, we quantified the quenching rate constant and observed that as the illumination proceeds the accumulation of the quencher leads to a speed up of the fluorescence decay of the PSII-684 compartment as the decay rate constant increases from about 3 to 4 ns(− 1). The quenching on PSII-684 leads to indirect quenching of the compartments PSII-690 and PSII-695 which represent the red chlorophyll of the PSII core. These results explain past and current observations of light-induced quenching in 77 K steady-state and time-resolved fluorescence spectra. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11120-018-0534-8) contains supplementary material, which is available to authorized users. Springer Netherlands 2018-06-13 2018 /pmc/articles/PMC6182390/ /pubmed/29948747 http://dx.doi.org/10.1007/s11120-018-0534-8 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Wlodarczyk, Lucyna M. Snellenburg, Joris J. Dekker, Jan P. Stokkum, Ivo H. M. Development of fluorescence quenching in Chlamydomonas reinhardtii upon prolonged illumination at 77 K |
title | Development of fluorescence quenching in Chlamydomonas reinhardtii upon prolonged illumination at 77 K |
title_full | Development of fluorescence quenching in Chlamydomonas reinhardtii upon prolonged illumination at 77 K |
title_fullStr | Development of fluorescence quenching in Chlamydomonas reinhardtii upon prolonged illumination at 77 K |
title_full_unstemmed | Development of fluorescence quenching in Chlamydomonas reinhardtii upon prolonged illumination at 77 K |
title_short | Development of fluorescence quenching in Chlamydomonas reinhardtii upon prolonged illumination at 77 K |
title_sort | development of fluorescence quenching in chlamydomonas reinhardtii upon prolonged illumination at 77 k |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182390/ https://www.ncbi.nlm.nih.gov/pubmed/29948747 http://dx.doi.org/10.1007/s11120-018-0534-8 |
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