Redox transients of P680 associated with the incremental chlorophyll-a fluorescence yield rises elicited by a series of saturating flashes in diuron-treated photosystem II core complex of Thermosynechococcus vulcanus
Language English Country Denmark Media print-electronic
Document type Journal Article
Grant support
LP2014/19
Lendület Program of the Hungarian Academy of Sciences
31470339
National Natural Science Foundation of China
XDB17000000
Strategic Priority Research Program of Chinese Academy of Sciences
2017YFA0503700
National Key R&D Program of China
French Infrastructure for Integrated Structural Biology (FRISBI) ANR-10-INBS-05
EBSA
124985
National Research Development and Innovation Office of Hungary
K 128679
National Research Development and Innovation Office of Hungary
TÉT_15-1-2016-0144
National Research Development and Innovation Office of Hungary
124904
National Research Development and Innovation Office of Hungary
GINOP-2.3.2-15-2016-00001
National Research Development and Innovation Office of Hungary
PubMed
30790299
DOI
10.1111/ppl.12945
Knihovny.cz E-resources
- MeSH
- Chlorophyll A metabolism MeSH
- Photosystem II Protein Complex metabolism MeSH
- Oxidation-Reduction MeSH
- Cyanobacteria metabolism MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Chlorophyll A MeSH
- Photosystem II Protein Complex MeSH
Recent chlorophyll-a fluorescence yield measurements, using single-turnover saturating flashes (STSFs), have revealed the involvement of a rate-limiting step in the reactions following the charge separation induced by the first flash. As also shown here, in diuron-inhibited PSII core complexes isolated from Thermosynechococcus vulcanus the fluorescence maximum could only be reached by a train of STSFs. In order to elucidate the origin of the fluorescence yield increments in STSF series, we performed transient absorption measurements at 819 nm, reflecting the photooxidation and re-reduction kinetics of the primary electron donor P680. Upon single flash excitation of the dark-adapted sample, the decay kinetics could be described with lifetimes of 17 ns (∼50%) and 167 ns (∼30%), and a longer-lived component (∼20%). This kinetics are attributed to re-reduction of P680•+ by the donor side of PSII. In contrast, upon second-flash (with Δt between 5 μs and 100 ms) or repetitive excitation, the 819 nm absorption changes decayed with lifetimes of about 2 ns (∼60%) and 10 ns (∼30%), attributed to recombination of the primary radical pair P680•+ Pheo•- , and a small longer-lived component (∼10%). These data confirm that only the first STSF is capable of generating stable charge separation - leading to the reduction of QA ; and thus, the fluorescence yield increments elicited by the consecutive flashes must have a different physical origin. Our double-flash experiments indicate that the rate-limiting steps, detected by chlorophyll-a fluorescence, are not correlated with the turnover of P680.
Faculty of Science University of Ostrava Ostrava Czech Republic
Photosynthesis Research Center Institute of Botany Chinese Academy of Sciences Beijing China
Photosynthesis Research Center Okayama University Okayama Japan
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