Formate-induced inhibition of the water-oxidizing complex of photosystem II studied by EPR.

The effects of various formate concentrations on both the donor and the acceptor sides in oxygen-evolving PS II membranes (BBY particles) were examined. EPR, oxygen evolution and variable chlorophyll fluorescence have been observed. It was found that formate inhibits the formation of the S(2) state multiline signal concomitant with stimulation of the Q(A)(-)Fe(2+) signal at g = 1.82. The decrease and the increase in intensities of the multiline and Q(A)(-)Fe(2+) signals, respectively, had a linear relation for formate concentrations between 5 and 500 mM. The g = 4.1 signal formation measured in the absence of methanol was not inhibited by formate up to 250 mM in the buffer. In the presence of 3% methanol the g = 4.1 signal evolved as formate concentration increased. The evolved signal could be ascribed to the inhibited centers. Oxygen evolution measured in the presence of an electron acceptor, phenyl-p-benzoquinone, was also inhibited by formate proportionally to the decrease in the multiline signal intensity. The inhibition seemed to be due to a retarded electron transfer from the water-oxidizing complex to Y(Z)(+), which was observed in the decay kinetics of the Y(Z)(+) signal induced by illumination above 250 K. These results show that formate induces inhibition of water oxidation reactions as well as electron transfer on the PS II acceptor side. The inhibition effects of formate in PS II were found to be reversible, indicating no destructive effect on the reaction center induced by formate.

Stabilization of oxygen evolution and primary electron transport reactions in photosystem II against heat stress with glycinebetaine and sucrose.

The protective action of co-solutes, such as sucrose and glycinebetaine, against the thermal inactivation of photosystem II function was studied in untreated and Mn-depleted photosystem II preparations. It was shown that, in addition to the reactions that depend on the oxygen evolving activity of the photosystem, those that implicate more intimately the reaction center itself are protected by high concentrations of osmolytes. However, the temperature required to inhibit oxygen evolution totally in the presence of osmolytes is lower than that required to eliminate reactions, such as P680 (primary electron donor in photosystem II) photo-oxidation and pheophytin photo reduetion, which only involve charge separation and primary electron transport processes. The energy storage measured from the thermal dissipation yield during photoacoustic experiments and the yield of variable fluorescence are also protected to a significant degree (up to 30%) at temperatures at which oxygen evolution is totally inhibited. It is suggested that a cyclic electron transport reaction around photosystem II may be preserved under these conditions and may be responsible for the energy storage measured at relatively high temperatures. This interpretation is also supported by thermoluminescence data involving the recombination between reduced electron acceptors and oxidized electron donors at - 30 and - 55 °C. The data also imply that a high concentration of osmolyte allows the stabilization of the photosystem core complex together with the oxygen-evolving complex. The stabilization effect is understood in terms of the minimization of protein-water interactions as proposed by the theory of Arakawa and Timasheff (Biophys. J., 47 (1985) 411--414).

Effects of bicarbonate and formate on the donor side of Photosystem 2.

Sodium formate at concentration of 5-20 µM suppresses electron flow on the donor side of Photosystem 2 (PS 2) in pea subchloroplast membranes (DT-20) which is revealed by inhibition of photoinduced changes of chlorophyll fluorescence yield related to photoreduction of QA and pheophytin (the primary and intermediary electron acceptors) and oxygen evolution and the increase of absorbance changes related to photooxidation of P680, the primary electron donor, under continuous illumination. These activities are also inhibited upon partial depletion of bicarbonate in the medium and restored by the addition of 0.1-10 mM NaHCO3. At concentrations higher than 20 µM formate induces the known bicarbonate effect on the acceptor side of PS 2 which dominates at millimolar concentrations of the agent. In Tris-treated (Mn-depleted) DT-20 the restoration of electron flow with 0.2 µM MnCl2 (4 Mn atoms per one PS 2 reaction center) in the medium depleted of bicarbonate is efficient only after the addition of 5 mM NaHCO3. The restoration in the presence of NaHCO3 is accompanied by an increased functional binding of Mn(2+) to PS 2 membranes which is confirmed by experiments on removal of added Mn(2+) by either sedimentation or the addition of EDTA. Pre-illumination increases the Mn binding in the presence of bicarbonate. The data show that the bicarbonate effect on the donor side of PS 2 is related to a relatively low-affinity bound pool of bicarbonate. It is suggested that bicarbonate takes part in the formation of the Mn-cluster capable of water oxidation as an obligatory ligand or through modification of the binding site(s) of Mn.