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      Changing frequency of fluctuating light reveals the molecular mechanism for P700 oxidation in plant leaves

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          Abstract

          Natural sunlight exceeds the demand of photosynthesis such that it can cause plants to produce reactive oxygen species ( ROS), which subsequently cause photo‐oxidative damage. Because photosystem I ( PSI) is a major source of ROS, plants actively maintain the reaction center chlorophyll of PSI(P700) oxidized under excessive light conditions to alleviate the ROS production. P700 oxidation is universally recognized in photosynthetic organisms as a physiological response to excessive light. However, it is still poorly understood how P700 oxidation is induced in response to fluctuating light with a variety of frequencies. Here, we investigated the relationships of photosynthetic parameters with P700 oxidation in Arabidopsis thaliana under a sine fluctuating light with different frequencies. As the photon flux density of the light increased, P700 was oxidized concurrently with the chlorophyll fluorescence parameter qL unless the electron acceptor side of PSI was limited. Conversely, we did not observe a proportional relationship of non‐photochemical quenching with P700 oxidation. The mutant crr‐2, which lacks chloroplast NADPH dehydrogenase, was impaired in P700 oxidation during light fluctuation at high, but not low frequency, unlike the pgrl1 mutant deficient in PGR5 and PGRL1 proteins, which could not oxidize P700 during light fluctuation at both high and low frequencies. Taken together, our findings suggested that the changing frequency of fluctuating light reveals the tracking performance of molecular mechanisms underlying P700 oxidation.

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          Most cited references57

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          Chlorophyll fluorescence as a tool in plant physiology : II. Interpretation of fluorescence signals.

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            In vivo modulation of nonphotochemical exciton quenching (NPQ) by regulation of the chloroplast ATP synthase.

            Nonphotochemical quenching (NPQ) of excitation energy, which protects higher plant photosynthetic machinery from photodamage, is triggered by acidification of the thylakoid lumen as a result of light-induced proton pumping, which also drives the synthesis of ATP. It is clear that the sensitivity of NPQ is modulated in response to changing physiological conditions, but the mechanism for this modulation has remained unclear. Evidence is presented that, in intact tobacco or Arabidopsis leaves, NPQ modulation in response to changing CO(2) levels occurs predominantly by alterations in the conductivity of the CF(O)-CF(1) ATP synthase to protons (g(H)(+)). At a given proton flux, decreasing g(H)(+) will increase transthylakoid proton motive force (pmf), thus lowering lumen pH and contributing to the activation of NPQ. It was found that an approximately 5-fold decrease in g(H)(+) could account for the majority of NPQ modulation as atmospheric CO(2) was decreased from 2,000 ppm to 0 ppm. Data are presented that g(H)(+) is kinetically controlled, rather than imposed thermodynamically by buildup of DeltaG(ATP). Further results suggest that the redox state of the ATP synthase gamma-subunit thiols is not responsible for altering g(H)(+). A working model is proposed wherein g(H)(+) is modulated by stromal metabolite levels, possibly by inorganic phosphate.
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              An improved method, using saturating light pulses, for the determination of photosystem I quantum yield via P700+-absorbance changes at 830 nm

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                Author and article information

                Contributors
                cmiyake@hawk.kobe-u.ac.jp
                Journal
                Plant Direct
                Plant Direct
                10.1002/(ISSN)2475-4455
                PLD3
                Plant Direct
                John Wiley and Sons Inc. (Hoboken )
                2475-4455
                23 July 2018
                July 2018
                : 2
                : 7 ( doiID: 10.1002/pld3.2018.2.issue-7 )
                : e00073
                Affiliations
                [ 1 ] Department of Biological and Environmental Science Faculty of Agriculture Graduate School of Agricultural Science Kobe University Kobe Japan
                [ 2 ] Core Research for Environmental Science and Technology Japan Science and Technology Agency Tokyo Japan
                Author notes
                [*] [* ] Correspondence

                Chikahiro Miyake, Department of Biological and Environmental Science, Faculty of Agriculture, Graduate School of Agricultural Science, Kobe University, 1‐1 Rokkodai, Nada, Kobe 657‐8501, Japan.

                Email: cmiyake@ 123456hawk.kobe-u.ac.jp

                Article
                PLD373
                10.1002/pld3.73
                6508772
                7462716a-0180-46ed-a040-e17957c3b268
                © 2018 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.

                History
                : 20 November 2017
                : 05 April 2018
                : 15 June 2018
                Page count
                Figures: 4, Tables: 0, Pages: 11, Words: 8579
                Funding
                Funded by: Japan Society for the Promotion of Science
                Award ID: 26450079
                Award ID: 16J03443
                Funded by: Core Research for Evolutional Science and Technology (CREST) division of the Japan Science and Technology Agency
                Award ID: AL65D21010
                Categories
                Original Research
                Original Research
                Custom metadata
                2.0
                pld373
                July 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.1 mode:remove_FC converted:27.03.2019

                fluctuating light,p700 oxidation,photosynthesis,reactive oxygen species

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