Two rice chlorophyll (Chl) b-less mutants (VG28-1, VG30-5) and the respective wild type (WT) plant (cv. Zhonghua No. 11) were analyzed for the changes in Chl fluorescence parameters, xanthophyll cycle pool, and its de-epoxidation state under exposure to strong irradiance, SI (1 700 µmol m-2 s-1). We also examined alterations in the chloroplast ultrastructure of the mutants induced by methyl viologen (MV) photooxidation. During HI (0-3.5 h), the photoinactivation of photosystem 2 (PS2) appeared earlier and more severely in Chl b-less mutants than in the WT. The decreases in maximal photochemical efficiency of PS2 in the dark (Fv/Fm), quantum efficiency of PS2 electron transport (ΦPS2), photochemical quenching (qP), as well as rate of photochemistry (Prate), and the increases in de-epoxidation state (DES) and rate of thermal dissipation of excitation energy (Drate) were significantly greater in Chl b-mutants compared with the WT plant. A relatively larger xanthophyll pool and 78-83 % conversion of violaxanthin into antheraxanthin and zeaxanthin in the mutants after 3.5 h of HI was accompanied with a high ratio of inactive/total PS2 (0.55-0.73) and high 1-qP (0.57-0.68) which showed that the activities of the xanthophyll cycle were probably insufficient to protect the photosynthetic apparatus against photoinhibition. No apparent difference of chloroplast ultrastructure was found between Chl b-less mutants and WT plants grown under low, LI (180 µmol m-2 s-1) and high, HI (700 µmol m-2 s-1) irradiance. However, swollen chloroplasts and slight dilation of thylakoids occurred in both mutants and the WT grown under LI followed by MV treatment. These typical symptoms of photooxidative damage were aggravated as plants were exposed to HI. Distorted and loose scattered thylakoids were observed in particular in the Chl b-less mutants. A greater extent of photoinhibition and photooxidation in these mutants indicated that the susceptibility to HI and oxidative stresses was enhanced in the photosynthetic apparatus without Chl b most likely as a consequence of a smaller antenna size. and Z.-F. Lin, G.-Z. Lin, C.-L. Peng.
Photoinactivation of photosystem 2 (PS2) results from absorption of so-called "excessive" photon energy. Chlorophyll a fluorescence can be applied to quantitatively estimate the portion of excessive photons by means of the parameter E = (F - F0')/Fm', which reflects the share of the absorbed photon energy that reaches the reaction centers (RCs) of PS2 complexes with QA in the reduced state ('closed' RCs). Data obtained for cotton (Gossypium hirsutum), bean (Phaseolus vulgaris), and arabidopsis (Arabidopsis thaliana) suggest a linear relationship between the total amount of the photon energy absorbed in excess (excessive irradiation) and the decline in PS2 activity, though the slope may differ depending on the species. This relationship was sensitive not only to the leaf temperature but also to treatment with methyl viologen. Such observations imply that the intensity of the oxidative stress as well as the plant's ability to detoxify active oxygen species may interact to determine the damaging potential of the excessive photons absorbed by PS2 antennae. Energy partitioning in PS2 complexes was adjusted during adaptation to irradiation and in response to a decrease in leaf temperature to minimize the excitation energy that is trapped by 'closed' PS2 RCs. The same amount of the excessive photons absorbed by PS2 antennae led to a greater decrease in PS2 activity at warmer temperatures, however, the delay in the development of non-photochemical and photochemical energy quenching under lower temperature resulted in faster accumulation of excessive photons during induction. Irradiance response curves of EF suggest that, at high irradiance (above 700 μmol m-2 s-1), steady-state levels of this parameter tend to be similar regardless of the leaf temperature. and D. Kornyeyev, A. S. Holaday, B. A. Logan.
Photon-induced absorbance changes at 830 nm (ΔA830) related to redox transformations of P700, primary electron donor of photosystem 1 (PS1), were examined in barley leaves treated with diuron and methyl viologen. In such leaves, only soluble reductants localized in chloroplast stroma could serve as electron donors for P700+. Δ A830 were induced by 1-min irradiation of leaves with "actinic light" (AL, 700±6 nm) of various irradiances. Two exponentially decaying components with half-times of 2.75 (fast component, relative magnitude of 62 % of ΔA830) and 11.90 s (slow one, 38 % of ΔA830) were distinguished in the kinetics of dark relaxation of ΔA830 after leaf irradiation with saturating AL. The components reflecting P700+ dark reduction in two units of PS1 differed in the rate of electron input from stromal reductants. The decline in AL irradiance reduced steady state δA830 magnitude, which was also accompanied by a decrease in the contribution of fast component to the overall P700+ dark reduction kinetics. The photon-response curves were obtained separately for rapidly and slowly decaying δA830. The values of half-saturating irradiance were 0.106 and 0.035 μmol m-2 s-1 for rapidly and slowly reduced PS1 units, respectively. The ratio of rate constants of P700+ dark reduction for rapidly and slowly reduced PS1 units was 1.4 times higher than the ratio of their half-saturating irradiances thus indicating higher relative antenna size in rapidly reduced PS1 units. The latter finding, taken together with higher relative amount of P700, favours the view that rapidly and slowly reduced PS1 units reflect P700+ reduction by stromal reductants in spatially separated PS1α and PS1β complexes. and E. A. Egorova, N. G. Bukhov.