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

. 2019 May ; 166 (1) : 22-32. [epub] 20190318

Jazyk angličtina Země Dánsko Médium print-electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid30790299

Grantová podpora
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

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.

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