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F. Allen, J. Franck (1955)
Photosynthetic evolution of oxygen by flashes of light.Archives of biochemistry and biophysics, 58 1
C. Weiss, K. Sauer (1969)
ACTIVATION KINETICS OF PHOTOSYNTHETIC OXYGEN EVOLUTION UNDER 20–40 NANOSECOND LASER FLASHESPhotochemistry and Photobiology, 11
P. Bennoun (1970)
Réoxydation du quencher de fluorescence “Q” en présence de 3-(3,4-dichlorophényl)-1,1-diméthyluréeBiochimica et Biophysica Acta, 216
W. Arthur, B. Strehler (1957)
Studies on the primary process in photosynthesis. I. Photosynthetic luminescence; multiple reactants.Archives of biochemistry and biophysics, 70 2
Mordhay Avron (1960)
Photophosphorylation by swiss-chard chloroplasts.Biochimica et biophysica acta, 40
G. Barbieri, R. Delosme, Pierre Joliot (1970)
COMPARAISON ENTRE L'EMISSION D'OXYGENE ET L'EMISSION DE LUMINESCENCE A LA SUITE D'UNE SERIE D'ECLAIRS SATURANTSPhotochemistry and Photobiology, 12
Pierre Joliot, G. Barbieri, R. Chabaud (1969)
UN NOUVEAU MODELE DES CENTRES PHOTOCHIMIQUES DU SYSTEME II *Photochemistry and Photobiology, 10
L. Jones (1967)
Two quantum-hit requirement for delayed light emission from photosynthetic green algae.Proceedings of the National Academy of Sciences of the United States of America, 58 1
Pierre Joliot (1961)
N° 50. — Cinétique d’induction de la photosynthèse chez Chlorella pyrenoidosa - II. — Cinétique d’émission d’oxygène et fluorescence pendant la phase initiale d’illumination, 58
R. Clayton (1969)
Characteristics of prompt and delayed fluorescence from spinach chloroplasts.Biophysical journal, 9 1
(1970)
Currents in Photosynthesis
Pierre Joliot (1965)
Cinétiques des réactions liées a l'émission d'oxygène photosynthétiqueBiochimica et Biophysica Acta, 102
P. Bennoun, A. Joliot (1969)
Etude de la photooxydation de l'hydroxylamine par les chloroplastes d'epinardsBiochimica et Biophysica Acta, 189
Pierre Joliot (1965)
Études simultanées des cinétiques de fluorescence et d'émission d'oxygène photosynthétiqueBiochimica et Biophysica Acta, 102
Bliss Forbush, Bessel Kok (1968)
Reaction between primary and secondary electron acceptors of photosystem II of photosynthesis.Biochimica et biophysica acta, 162 2
Bernadette Bouges (1971)
Action de faibles concentrations d'hydroxylamine sur l'emission d'oxygene des algues Chlorella et des chloroplastes d'epinardsBiochimica et Biophysica Acta, 234
B. Kok, B. Forbush, Marion McGLOIN (1970)
COOPERATION OF CHARGES IN PHOTOSYNTHETIC O2 EVOLUTION–I. A LINEAR FOUR STEP MECHANISMPhotochemistry and Photobiology, 11
P. Joliot, A. Joliot (1968)
A polarographic method for detection of oxygen production and reduction of hill reagent by isolated chloroplasts.Biochimica et biophysica acta, 153 3
R. Delosme (1967)
Étude de l'induction de fluorescence des algues vertes et des chloroplastes au début d'une illumination intense☆Biochimica et Biophysica Acta, 143
(1970)
Forbush and B . Kok , Biochim . Biophys
P. Joliot (1968)
KINETIC STUDIES OF PHOTOSYSTEM II IN PHOTOSYNTHESIS *Photochemistry and Photobiology, 8
Abstract— New results are presented on the emission of oxygen by algae and chloroplasts illuminated by a sequence of short saturating flashes. These results favor the four‐state hypothesis of Kok and co‐workers, in which formation of oxygen requires the accumulation of four oxidants produced by four successive photoreactions. Deactivation of the more oxidized precursor states in the dark is studied under different conditions of preillumination. Our results suggest that both a one step and a two step mechanism of deactivation exist. In order to understand the biological significance of Kok's parameter α—the fraction of photochemical centers unable to react on each flash (“misses”)‐we study reoxidation of acceptor Q after one flash by fluorescence techniques. It appears that a fraction of Q‐ is reoxidized by a back reaction which cancels the effect of the preilluminating flash and is probably responsible for the misses. The results of some luminescence experiments are also reported. These experiments demonstrate that delayed emission of light is associated with the deactivation of states S2 and S3. It is possible that excitons produced by deactivation can be reabsorbed by active photochemical centers, which can modify considerably the deactivation process.
Photochemistry & Photobiology – Wiley
Published: Sep 1, 1971
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