The decay of tyrosine cation radical was found to be biphasic at 253 K. The fast phase corresponds to the YZ* component while the slow phase corresponds to the tyrosine D radical (YD*) component. At 253 K, the t1/2 value was ∼28.6 s for the fast phase and ∼190.7 s for the slow phase. The fast phase is attributed to the recombination of charges between YZ* and QA-. The activation energy for the reaction of YZ with QA- between 253 and 293 K was 48 kJ mol-1 in Cl--depleted photosystem 2 (PS2) membranes. Both the decay rate and the amplitude of the PAR-induced signal of YZ* were affected by addition of chloride anion. Change in the decay rate and the amplitude of the PAR-induced signal of YZ* was observed when other anions like Br-, I-, F, HCO3-, NO3-, PO43- were substituted in the Cl--depleted PS2. and A. Jajoo, S. Bharti, A. Kawamori.
In our study, one-month-old Melissa officinalis plants were subjected to Fe-deficiency treatments, such as 10 µM Fe (as direct iron deficiency, DD), and 30 µM Fe + 10 mM NaHCO3 + 0.5 g l-1 CaCO3 (as indirect iron deficiency, ID), and 30 µM Fe (as control) for 14 d. Both Fe-deficiency types reduced plant growth, photosynthetic pigment contents, an active Fe content in roots and leaves, root Fe(III)-reducing capacity, Fe-use efficiency, maximal quantum yield of PSII photochemistry, a ratio of variable to basic fluorescence, and activities of antioxidant enzymes, while they increased lipid peroxidation and a H2O2 content in leaves. These effects were more pronounced in plants exposed to ID with bicarbonate than those of DD plants. We showed that sodium nitroprusside (SNP), as NO donor, could ameliorate the adverse effects of bicarbonate on above traits. The methylene blue, as NO blocker, reversed the protective effects conferred by SNP in the ID-treated plants as well as DD plants. These findings suggests that NO protects photosynthesis and growth of IDtreated plants as well as DD plants by contribution in availability and/or delivery of metabolically active iron or by changing activities of reactive oxygen species-scavenging enzymes., R. Amooaghaie, Sh. Roohollahi., and Obsahuje bibliografii
Ionic environment is important in regulating photosynthetic reactions. The roles of cations, Mn2+, Mg2+, Ca2+, Na+, and K+ as cofactors in electron transport, energy transfer, phosphorylation, and carbon assimilation are better known than the roles of anions, except for chloride and bicarbonate. Only a limited information exists on the roles and effects of nitri formate, sulphate, and phosphate. In this review, we evaluate and highlight the roles of some specific anions on electron transport as well as on excitation energy transfer processes in photosynthesis. Anions exert significant effects on thyla membrane conformation and membrane fluidity, possibly by redistributing the thylakoid membrane surface charges. The anion/cation induced phase transitions in the hydrophilic domains of the thylakoid membranes are probably responsible for the various structural and co-related functional changes under stress. Anions are also important in regulation of energy distribution between the two photosystems. Anions do not only divert more energy from photosystem (PS) 2 to PS1, but can also reverse the effect of cations on energy distribution in a valence-dependent manner. Anions affect also the structure of the photosynthetic apparatus and excitation energy distribution between the two photosystems. and A. Jajoo, S. Bharti, P. Mohanty.
The PsbM (3.9 kDa) and PsbY (4.2 kDa) proteins are membrane-spanning, single-helix, subunits associated with the chlorophyll-binding CP47 pre-complex of photosystem II (PSII). Removal of PsbM resulted in accumulation of PSII pre-assembly complexes and impaired electron transfer between the primary (QA) and secondary (QB) plastoquinone electron acceptors of PSII indicating that the QB-binding site and bicarbonate binding to the non-heme iron were altered in this strain. Removal of PsbY alone had only a minor impact on PSII activity but deleting PsbY in the PsbM background led to additional modification of the acceptor side resulting in PsbM:PsbY cells being susceptible to photodamage and this required protein synthesis for recovery. Addition of bicarbonate was able to compensate for the light-induced damage in PsbM:PsbY cells potentially re-occupying the modified bicarbonate-binding site in the PsbM:PsbY strain and complementation of PsbM:PsbY cells with the psbY gene restored the PsbM phenotype., S. Biswas, J. J. Eaton-Rye., and Obsahuje bibliografické odkazy