Probing the kinetics of Photosystem I and Photosystem II fluorescence in pea chloroplasts on a picosecond pulse fluorometer

1975 ◽  
Vol 408 (2) ◽  
pp. 143-153 ◽  
Author(s):  
V.Z. Paschenko ◽  
S.P. Protasov ◽  
A.B. Rubin ◽  
K.N. Timofeev ◽  
L.M. Zamazova ◽  
...  
1994 ◽  
Vol 49 (1-2) ◽  
pp. 87-94 ◽  
Author(s):  
Klaus P. Bader ◽  
Susanne Höper

Alkylbenzyldimethylammonium chloride (ABDAC, zephirol) has been shown to improve the functioning of the photosynthetic apparatus of the filamentous cyanobacterium Oscillatoria chalybea (Bader, K. P. (1989) Biochim. Biophys. Acta 975, 399-402). This biocide exerts stimulatory effects on various electron transport reactions in Oscillatoria chalybea and chloroplasts from higher plants. By means of oxygen evolution measurements and of repetitive flash-induced absorption spectroscopy we were able to demonstrate an impact of the drug on the major complexes of photosynthetic membranes, i.e. the water splitting complex, photosystem II and photosystem I. Both, P820- and X320-absorption change signals were enhanced by the addition of ABDAC. Along with the quantitative analysis we investigated the relaxation kinetics of the signals and observed a substantial stabilization of the oxidized states of the respective redox components in the presence of the ammonium salt. Under appropriate conditions the relaxation kinetics of the absorption signals were significantly slowed down. ABDAC also affects photosystem I in Oscillatoria chalybea, but only under conditions, where a donor/acceptor system i.e. an isolated photosystem I reaction with photosystem II being disconnected was measured. Electron transport through the whole chain i.e. with water as the electron donor yielded no effect of the quaternary ammonium salt. It is suggested that this is due to an extremely bad linkage between the two photosystem, each of which, however, shows good reaction rates, when separately measured. The described interactions of the biocide with photosynthetic membranes are not restricted to Oscillatoria chalybea but are also observed with higher plant chloroplasts. In these systems, ABDAC enhances X320- and P700-signals to a comparable extent. In this case the P700-signal is stimulated in assays with electrons which are furnished from water which hints at good coupling between the two photosystems in our tobacco chloroplast preparations.


PLoS ONE ◽  
2012 ◽  
Vol 7 (1) ◽  
pp. e30167 ◽  
Author(s):  
Mia O. Hoogenboom ◽  
Douglas A. Campbell ◽  
Eric Beraud ◽  
Katrina DeZeeuw ◽  
Christine Ferrier-Pagès

1988 ◽  
Vol 43 (11-12) ◽  
pp. 871-876 ◽  
Author(s):  
Imre Vass ◽  
Narendranath Mohanty ◽  
Sándor Demeter

Abstract The effect of photoinhibition on the primary (QA) and secondary (QB) quinone acceptors of photosystem I I was investigated in isolated spinach thylakoids by the methods of thermoluminescence and delayed luminescence. The amplitudes of the Q (at about 2 °C) and B (at about 30 °C) thermoluminescence bands which are associated with the recombination of the S2QA- and S2QB charge pairs, respectively, exhibited parallel decay courses during photoinhibitory treatment. Similarly, the amplitudes of the flash-induced delayed luminescence components ascribed to the recombination of S20A and S2OB charge pairs and having half life-times of about 3 s and 30 s, respectively, declined in parallel with the amplitudes of the corresponding Q and B thermoluminescence bands. The course of inhibition of thermoluminescence and delayed luminescence intensity was parallel with that of the rate of oxygen evolution. The peak positions of the B and Q thermoluminescence bands as well as the half life-times of the corresponding delayed luminescence components were not affected by photoinhibition. These results indicate that in isolated thylakoids neither the amount nor the stability of the reduced OB acceptor is preferentially decreased by photoinhibition. We conclude that either the primary target of photodamage is located before the O b binding site in the reaction center of photosystem II or QA and OB undergo simultaneous damage.


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