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Dark recovery of the Chl a fluorescence transient (OJIP) after light adaptation: The qT-component of non-photochemical quenching is related to an activated photosystem I acceptor side
Authors:Gert Schansker  Szilvia Z Tóth  Reto J Strasser
Institution:Bioenergetics Laboratory, University of Geneva, Chemin des Embrouchis 10, CH-1254 Jussy, Geneva, Switzerland
Abstract:The dark recovery kinetics of the Chl a fluorescence transient (OJIP) after 15 min light adaptation were studied and interpreted with the help of simultaneously measured 820 nm transmission. The kinetics of the changes in the shape of the OJIP transient were related to the kinetics of the qE and qT components of non-photochemical quenching. The dark-relaxation of the qE coincided with a general increase of the fluorescence yield. Light adaptation caused the disappearance of the IP-phase (20-200 ms) of the OJIP-transient. The qT correlated with the recovery of the IP-phase and with a recovery of the re-reduction of P700+ and oxidized plastocyanin in the 20-200 ms time-range as derived from 820 nm transmission measurements. On the basis of these observations, the qT is interpreted to represent the inactivation kinetics of ferredoxin-NADP+-reductase (FNR). The activation state of FNR affects the fluorescence yield via its effect on the electron flow. The qT therefore represents a form of photochemical quenching. Increasing the light intensity of the probe pulse from 1800 to 15000 μmol photons m−2 s−1 did not qualitatively change the results. The presented observations imply that in light-adapted leaves, it is not possible to ‘close’ all reaction centers with a strong light pulse. This supports the hypothesis that in addition to QA a second modulator of the fluorescence yield located on the acceptor side of photosystem II (e.g., the occupancy of the QB-site) is needed to explain these results. Besides, some of our results indicate that in pea leaves state 2 to 1 transitions may contribute to the qI-phase.
Keywords:Chl  chlorophyll  DCMU  3-(3&prime    4&prime  -dichlorophenyl)-1  1-dimethylurea  Fo and Fm  fluorescence intensity measured when all photosystem II reaction centers are open or closed respectively  FNR  ferredoxin-NADP+-reductase  Fls  fluorescence intensity measured under steady state conditions  I820   nm  photocurrent  a measure for the transmitted light at 820   nm  I-level  fluorescence intensity at &sim     30   ms  J-level  fluorescence intensity at &sim       ms  LA  light adaptation  LED  light emitting diode  LHCII  light harvesting complex II  O-level  fluorescence intensity at 20   μs  OJIP-transient  fluorescence induction transient defined by the names of its intermediate steps  P-level  the maximum fluorescence level  P680 and P700  reaction center pigments of photosystem II and I respectively  PC  plastocyanin  QA and QB  primary and secondary quinone electron acceptors of photosystem II respectively  qE  qT  qI  non-photochemical quenching components with respectively the fastest  medium and slowest relaxation rates  qNsv  non-photochemical quenching calculated according to Stern-Volmer
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