ArticlePhotosynthesis research2012
Oxygen evolution and chlorophyll fluorescence from multiple turnover light pulses: charge recombination in photosystem II in sunflower leaves.
Article in Photosynthesis research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Excitation transfer and quenching in photosystem II, enlightened by carotenoid triplet state in leaves.Photosynthesis research · 2024Article
- Prying into the green black-box.Photosynthesis research · 2022Review
- Time- and reduction-dependent rise of photosystem II fluorescence during microseconds-long inductions in leaves.Photosynthesis research · 2020Article
- Variable fluorescence of closed photochemical reaction centers.Photosynthesis research · 2020Article
- Kinetics of photosystem II electron transport: a mathematical analysis based on chlorophyll fluorescence induction.Photosynthesis research · 2018Article
- Thermal phase and excitonic connectivity in fluorescence induction.Photosynthesis research · 2013Article
- Excitonic connectivity between photosystem II units: what is it, and how to measure it?Photosynthesis research · 2013Review
- Wavelength-dependent photodamage to Chlorella investigated with a new type of multi-color PAM chlorophyll fluorometer.Photosynthesis research · 2013Article
- Photosystem II antennae are not energetically connected: evidence based on flash-induced O2 evolution and chlorophyll fluorescence in sunflower leaves.Photosynthesis research · 2012Article
- The time course of photoinactivation of photosystem II in leaves revisited.Photosynthesis research · 2012Article
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3 authors.
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Abstract
Oxygen evolution and Chl fluorescence induction were measured during multiple turnover light pulses (MTP) of 630-nm wavelength, intensities from 250 to 8,000 μmol quanta m(-2) s(-1) and duration from 0.3 to 200 ms in sunflower leaves at 22 °C. The ambient O(2) concentration was 10-30 ppm and MTP were applied after pre-illumination under far-red light (FRL), which oxidized plastoquinone (PQ) and randomized S-states because of the partial excitation of PSII. Electron (e ( - )) flow was calculated as 4·O(2) evolution. Illumination with MTP of increasing length resulted in increasing O(2) evolution per pulse, which was differentiated against pulse length to find the time course of O(2) evolution rate with sub-millisecond resolution. Comparison of the quantum yields, Y (IIO) = e ( - )/hν from O(2) evolution and Y (IIF) = (F (m) - F)/F (m) from Chl fluorescence, detected significant losses not accompanied by fluorescence emission. These quantum losses are discussed to be caused by charge recombination between Q (A) (-) and oxidized TyrZ at a rate of about 1,000 s(-1), either directly or via the donor side equilibrium complex Q(A) → P (D1) (+) ↔ TyrZ(ox), or because of cycling facilitated by Cyt b (559). Predicted from the suggested mechanism, charge recombination is enhanced by damage to the water-oxidizing complex and by restricted PSII acceptor side oxidation. The rate of PSII charge recombination/cycling is fast enough for being important in photoprotection.
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