Conformational changes and their role in non-radiative energy dissipation in photosystem II reaction centres

2005 ◽  
Vol 4 (12) ◽  
pp. 999 ◽  
Author(s):  
Radek Litvín ◽  
David Bína ◽  
Pavel Šiffel ◽  
František Vácha
Keyword(s):  
Energy Dissipation ◽  
Photosystem Ii ◽  
Conformational Changes ◽  
Radiative Energy ◽  
Reaction Centres

Mangrove Photosynthesis: Response to High-Irradiance Stress

1988 ◽  
Vol 15 (2) ◽  
pp. 43 ◽  
Author(s):  
O Bjorkman ◽  
B Demmig ◽  
TJ Andrews
Keyword(s):  
Energy Dissipation ◽  
Photosystem Ii ◽  
Energy Conversion ◽  
O2 Evolution ◽  
Photon Yield ◽  
Mangrove Species ◽  
Reaction Centres ◽  
Fluorescence Characteristics ◽  
Shade Leaves ◽  
Sun Leaves

Efficiencies of photosynthetic energy conversion were determined in sun and shade leaves of several mangrove species, growing in an open intertidal habitat in North Queensland, by measuring the maximum photon yield of O2 evolution and 77K chlorophyll fluorescence characteristics. Preliminary meas- urements confirmed that mangrove leaves have low water potentials, low stomatal conductances and low light-saturated CO2 exchange rates. Mangrove sun leaves therefore received a very large excess of excitation energy. Mangrove shade leaves had as high a photon yield of O2 evolution as non-mangrove leaves and their fluorescence characteristics were normal, showing that the energy conversion efficiency was unaffected by the high salinity. Mangrove sun leaves had markedly depressed photon yields and fluorescence was severely quenched showing that the efficiency of the photochemistry of photosystem II was reduced. The efficiency of energy conversion decreased with an increased radiation receipt. No such depression was detected in sun leaves of non-mangrove species growing in adjacent non-saline sites. Shading of man- grove sun leaves resulted in an increase in the efficiency of energy conversion but, in most species, more than 1 week was required for these leaves to reach the efficiency of shade leaves. Leaves exposed to direct sunlight had somewhat higher efficiencies in mangrove plants cultivated in 10% seawater as compared with full-strength seawater but the salinity of the culture solution had little effect on the increase in the efficiency upon shading. Field and laboratory fluorescence measurements indicated that the reduced efficiency of energy conversion in mangrove sun leaves resulted from a large increase in the rate constant for radiationless energy dissipation in the antenna chlorophyll rather than from damage to the photosystem II reaction centres. We propose that this increase in radiationless energy dissipation serves to protect the reaction centres against damage by excessive excitation.

Conformational changes of the intermediate of the S2 to S3 transition in photosystem II

2011 ◽  
Vol 104 (1-2) ◽  
pp. 72-79 ◽  
Author(s):  
Maria Chrysina ◽  
Georgia Zahariou ◽  
Yiannis Sanakis ◽  
Nikolaos Ioannidis ◽  
Vasili Petrouleas
Keyword(s):  
Photosystem Ii ◽  
Conformational Changes

Variable stoichiometries of photosystem II to photosystem I reaction centres

1988 ◽  
Vol 17 (3) ◽  
pp. 277-281 ◽  
Author(s):  
W. S. Chow ◽  
Jan M. Anderson ◽  
A. B. Hope
Keyword(s):  
Photosystem Ii ◽  
Photosystem I ◽  
Reaction Centres

scholarly journals How to build a water-splitting machine: structural insights into photosystem II assembly

2020 ◽  
Author(s):  
Jure Zabret ◽  
Stefan Bohn ◽  
Sandra Schuller ◽  
Oliver Arnolds ◽  
Madeline Möller ◽  
...  
Keyword(s):  
Photosystem Ii ◽  
Water Splitting ◽  
Conformational Changes ◽  
Binding Pocket ◽  
Heme Iron ◽  
Structural Motif ◽  
Acceptor Side ◽  
Non Heme Iron ◽  
Assembly Intermediate ◽  
Stepwise Assembly

Abstract Biogenesis of photosystem II (PSII), nature’s water splitting catalyst, is assisted by auxiliary proteins that form transient complexes with PSII components to facilitate stepwise assembly events. Using cryo-electron microscopy, we solved the structure of such a PSII assembly intermediate with 2.94 Å resolution. It contains three assembly factors (Psb27, Psb28, Psb34) and provides detailed insights into their molecular function. Binding of Psb28 induces large conformational changes at the PSII acceptor side, which distort the binding pocket of the mobile quinone (QB) and replace bicarbonate with glutamate as a ligand of the non-heme iron, a structural motif found in reaction centers of non-oxygenic photosynthetic bacteria. These results reveal novel mechanisms that protect PSII from damage during biogenesis until water splitting is activated. Our structure further demonstrates how the PSII active site is prepared for the incorporation of the Mn4CaO5 cluster, which performs the unique water splitting reaction.

Kinetic response of photosystem II photochemistry in the cyanobacterium Spirulina platensis to high salinity is characterized by two distinct phases

1999 ◽  
Vol 26 (3) ◽  
pp. 283 ◽  
Author(s):  
Congming Lu ◽  
Giuseppe Torzillo ◽  
Avigad Vonshak
Keyword(s):  
Electron Transport ◽  
Quantum Yield ◽  
Photosystem Ii ◽  
Spirulina Platensis ◽  
High Salinity ◽  
Photochemical Quenching ◽  
Second Phase ◽  
Ps Ii ◽  
Reaction Centres ◽  
Two Phases

The kinetic response of photosystem II (PS II) photochemistry in Spirulina platensis(Norstedt M2 ) to high salinity (0.75 M NaCl) was found to consist of two phases. The first phase, which was independent of light, was characterized by a rapid decrease (15–50%) in the maximal efficiency of PS II photochemistry (Fv /Fm), the efficiency of excitation energy capture by open PS II reaction centres (Fv′/Fm′), photochemical quenching (qp) and the quantum yield of PS II electron transport (Φ PS II) in the first 15 min, followed by a recovery up to about 80–92% of their initial levels within the next 2 h. The second phase took place after 4 h, in which further decline in above parameters occurred. Such a decline occurred only when the cells were incubated in the light, reaching levels as low as 45–70% of their initial levels after 12 h. At the same time, non-photochemical quenching (qN) and Q B -non-reducing PS II reaction centres increased significantly in the first 15 min and then recovered to the initial level during the first phase but increased again in the light in the second phase. The changes in the probability of electron transfer beyond QA (ψo) and the yield of electron transport beyond QA (φ Eo), the absorption flux (ABS/RC) and the trapping flux (TRo /RC) per PS II reaction centre also displayed two different phases. The causes responsible for the decreased quantum yield of PS II electron transport during the two phases are discussed.

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