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.
The protein secondary structure and pigments' microenvironment in photosystem 1 (PS1) complexes were studied in the temperature range of 25-80 °C using Fourier transform infrared (FT-IR) and circular dichroism (CD) spectroscopy, respectively. Quantitative analysis of the component bands of the amide I band (1 700-1 600 cm-1) showed no significant change below 50 °C. However, apparent conformational changes occurred at 60 °C and further continued at 70 and 80 °C accompanied with transitions of secondary structure mainly from α-helix to the β-sheet structures. CD analysis demonstrated that the regular arrangement, viz. protein microenvironment of pigments of PS1 complexes, was destroyed by heat treatment which might come from the changes of protein secondary structure of PS1. The CD signals at 645 nm contributed by chlorophyll (Chl) b of light-harvesting complex 1 (LHC1) were easily destroyed at the beginning of heat treatment (25-60 °C). When temperature reached 70 and 80 °C, the CD signals at 478 nm contributed mainly by Chl b of LHC1 and 498 nm contributed by carotenoids decreased most rapidly, indicating that LHC1 was more sensitive to high temperature than core complexes. In addition, the oxygen uptake rate decreased by 90.81 % at 70 °C and was lost completely at 80 °C showing that heat treatment damaged the regular function of PS1 complexes. This may be attributed to heat-induced changes of pigment microenvironment and protein secondary structure, especially transmembrane α-helix located in PsaA/B of PS1. and Z.-H. Hu ... [et al.].
Cations such as Mg2+ regulate spillover of absorbed excitation energy mainly in favour of photosystem (PS) 2. Effect of low concentration (<10 mM) of the monovalent cation Na+ on chlorophyll (Chl) a fluorescence was completely overridden by divalent cation Mg2+ (5 mM). Based on Chl a fluorescence yield and 77 K emission measurements, we revealed the role and effectiveness of anions (Cl-, SO42-, PO43-) in lowering the Mg2+-induced PS2 fluorescence. The higher the valency of the anion, the lesser was the expression of Mg2+ effect. Anions may thus overcome Mg2+ effects up to certain extent in a valency dependent manner, thereby diverting more energy to PS1 even in the presence of MgCl2. They may do so by reversing Mg2+-induced changes. and Anjana Jajoo, Sudhakar Bharti.
The aim of our study was to investigate the role of protons in regulating energy distribution between the two photosystems in the thylakoid membranes. Low pH-induced changes were monitored in the presence of a proton blocker, N,N′-dicyclohexylcarbodiimide (DCCD). When thylakoid membranes were suspended in a low-pH reaction mixture and incubated with DCCD, then a decrease in the fluorescence intensity of photosystem II (PSII) was observed, while no change in the intensity of photosystem I (PSI) fluorescence occurred according to the measured fluorescence emission spectra at 77 K. Since low pH induced distribution of energy from PSII to PSI was inhibited in the presence of DCCD, we concluded that pH/proton concentration of the thylakoid membranes plays an important role in regulating the distribution of the absorbed excitation energy between both photosystems., T. Tongra, S. Bharti, A. Jajoo., and Obsahuje bibliografii
The relationship between the activity of xanthophyll cycle and chlorophyll (Chl) metabolism was investigated using two cultivars, Helan No. 3 (seawater-tolerant cultivar) and Yuanye (seawater-sensitive cultivar), of spinach (Spinacia oleracea L.) plants cultured in Hoagland's nutrient solution, with or without seawater (40%). The results showed that, in plants of two cultivars with seawater, the xanthophyll cycle seems to show a principal protection mechanism against photoinhibition under seawater stress. Furthermore, accumulation of reactive oxygen species (ROS) in chloroplasts of two cultivars was enhanced by seawater to lower the activity of porphobilinogen deaminase. Namely, the conversion of porphobilinogen into uroporphyrinogen III involved in Chl biosynthetic processes was inhibited by seawater. In Helan No. 3 spinach plants with seawater, higher activity of xanthophyll cycle in the leaves dissipated more excess light energy, which appeared to lower the levels of ROS in chloroplasts. As a consequence, the Chl biosynthesis in Helan No. 3 leaves with seawater showed only a weak inhibition and the activity of chlorophyllase (Chlase) was not affected by seawater stress. In contrast, a more pronounced accumulation of ROS in chloroplasts of Yuanye leaves, which possess lower xanthophyll cycle activity, severely inhibited Chl biosynthesis and remarkably enhanced the activity of Chlase, which aggravates the decomposition of Chl. These results suggest that higher activity of xanthophyll cycle in seawater-tolerant spinach plays a role in maintaining Chl metabolic processes, probably by decreasing the levels of ROS, when the plants are cultured in the nutrient solution with seawater (40%). and J. Sun ... [et al.].
Three extrinsic polypeptides and manganese cluster were sequentially released from the membrane when photosystem 2 (PS2) membranes were kept under high hydrostatic pressure. The 17 kDa polypeptide was the most sensitive, while the 33 kDa polypeptide was the most reluctant to the treatment with high pressure. The release of manganese was not simply correlated with the loss of 33 kDa polypeptide. The losing of oxygen-evolving activity of PS2 was synchronised with the releasing of extrinsic polypeptides and manganese. and Y. Yu ... [et al.].