Cited by 161Photosynthetic Processes and MechanismsPlant Stress Responses and TolerancePlant biochemistry and biosynthesis

The Physiological Role of Ascorbate as Photosystem II Electron Donor: Protection against Photoinactivation in Heat-Stressed Leaves

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Tóth, Szilvia Z., Nagy, Valéria, Puthur, Jos T., Kovács, László, Garab, Győző·2011·Plant Physiology

Abstract

Previously, we showed that ascorbate (Asc), by donating electrons to photosystem II (PSII), supports a sustained electron transport activity in leaves in which the oxygen-evolving complexes were inactivated with a heat pulse (49°C, 40 s). Here, by using wild-type, Asc-overproducing, and -deficient Arabidopsis (Arabidopsis thaliana) mutants (miox4 and vtc2-3, respectively), we investigated the physiological role of Asc as PSII electron donor in heat-stressed leaves (40°C, 15 min), lacking active oxygen-evolving complexes. Chlorophyll-a fluorescence transients show that in leaves excited with trains of saturating single-turnover flashes spaced 200 ms apart, allowing continual electron donation from Asc to PSII, the reaction centers remained functional even after thousands of turnovers. Higher flash frequencies or continuous illumination (300 μmol photons m−2 s−1) gradually inactivated them, a process that appeared to be initiated by a dramatic deceleration of the electron transfer from TyrZ to P680+, followed by the complete loss of charge separation activity. These processes occurred with half-times of 1.2 and 10 min, 2.8 and 23 min, and 4.1 and 51 min in vtc2-3, the wild type, and miox4, respectively, indicating that the rate of inactivation strongly depended on the Asc content of the leaves. The recovery of PSII activity, following the degradation of PSII proteins (D1, CP43, and PsbO), in moderate light (100 μmol photons m−2 s−1, comparable to growth light), was also retarded in the Asc-deficient mutant. These data show that high Asc content of leaves contributes significantly to the ability of plants to withstand heat-stress conditions.

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Crossref · 10.1104/pp.110.171918

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  • Substantially high temperature inactivates the oxygen-evolving complex of PSII.

    “Substantially high temperature has been reported to inactivate the OEC of PSII (Zhang et al. 2001, Toth et al. 2011).”

    From Photosynthesis under stressful environments: An overview (2013) · cites this paper as Toth et al. 2011

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Authors
Tóth, S. Z., Nagy, V., Puthur, J. T., Kovács, L., & Garab, G.
Affiliations
HUN-REN Szegedi Biológiai Kutatóközpont (HU)
Venue
Plant Physiology
Published
2011-02-28
Volume
156
Issue
1
Pages
382-392
ISSN
  • 0032-0889 (ISSN-L)
  • 1532-2548
OpenAlex
W2108171248
Cited by
161
References
0
Citations by year
2026: 5 · 2025: 8 · 2024: 11 · 2023: 16 · 2022: 14 · 2021: 8 · 2020: 19 · 2019: 10 · 2018: 11 · 2017: 13 · 2016: 3 · 2015: 15 · 2014: 9 · 2013: 6 · 2012: 8
FWCI
3.64
Type
journal article
Language
en
Open access
Locations
  • PLANT PHYSIOLOGY (publishedVersion, cc-by)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Arkansas State University
  • Magyar Tudományos Akadémia
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Stress Responses and Tolerance
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant biochemistry and biosynthesis
Keywords
vitamin C, photosystem II, photoinactivation, heat stress, electron transport, oxygen-evolving complex, chlorophyll fluorescence, Arabidopsis thaliana, heat tolerance
MeSH terms
Ascorbic Acid, Electron Transport, Electrons, Fluorescence, Genotype, Hot Temperature, Light, Mutation, Oxidation-Reduction, Phenotype, Phosphoric Monoester Hydrolases, Stress, Physiological, Arabidopsis, Plant Leaves, Arabidopsis Proteins, Photosystem II Protein Complex

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