In comparison to cv. Torsdag, in leaves of low-productive Pisum sativum L. chlorophyll mutants the decrease in chlorophyll content was caused by the decrease in cell number per unit volume. Qualitative changes in activities of photosystem (PS) 1 in mutant M2004, and quantitative changes of PS1 and PS2 in mutants M2004 and M2014 and in hybrids were also found. However, the activity of ribulose-1,5-bisphosphate carboxylase (RuBPC) in M2014, and those of RuBPC and glyceraldehyde phosphate dehydrogenase in M2004 and hybrids were higher than in cv. Torsdag. The hybrids inherited the normal structure of photosynthetic apparatus of standard genotype in parallel with the compensatory gene complex of M2004, which was expressed at many levels of organization. This may be the basis of hybrid vigour in this case. and O. B. Vaishlya ... [et al.].
Chlorophyll a fluorescence induction measured by a fluorometer with a high temperature stressed plant material shows a new K step which is a clear peak due to fast fluorescence rise and subsequent decrease of fluorescence intensity. We focused on an explanation of the decrease of fluorescence after the K step using artificial electron acceptors and donors to photosystem 2 (PS2). Addition of the artificial electron acceptors or donors suppressed the decrease of fluorescence after the K step. We suggest that the decrease mainly reflects (by more than 81 %) an energy loss process in the reaction centre of PS2 which is most probably a nonradiative charge recombination between P680+ (oxidised primary electron donor in PS2) and a negative charge stored on either Pheo- or QA- (reduced primary electron acceptor of PS2 and reduced primary quinone electron acceptor of PS2, respectively). We suggest that the energy loss process is only possible when the inhibition of both the donor and the acceptor sides of PS2 occurs. and D. Lazár, P. Pospíšil, J. Nauš.
Irradiation of etiolated leaves leads to their greening. Although this problem has a long history, the question of whether the intermittent irradiation (IMI) grown plants have fully functional reaction centres as well as the oxygen clock, before exposure to continuous irradiation (CI), had not been resolved. To answer this question, as well as to analyze the development of the two photosystems, the following parallel measurements were made: (1) Emission spectra at 77 K; (2) OJIP chlorophyll (Chl) a fluorescence transient; (3) period 4 oscillation in the flash number dependence of initial fluorescence F0 (at 50 µs) and FJ (at 2 ms); and (4) P700. In the 1-ms-flash (FL) grown pea, that has a different biogenesis of the photosynthetic apparatus, delayed light emission (DLE) and Chl a fluorescence transient were measured in parallel. Quantitative analysis of Chl a fluorescence values provided the following conclusions: (1) IMI, not FL, plants have almost fully developed reaction centres and the oxygen clock. (2) Further greening of IMI plants under CI involves two phases: (a) during 3-4 h of CI, the number of PS2 units and connectivity between them increase, and then (b) light-harvesting antenna increases. (3) In FL, 10 min CI activates fully the oxygen clock. and A. Srivastava, R. J. Strasser, Govindjee.
Chlorophyll (Chl) fluorescence decay measurements were performed on higher plant leaves to investigate the photoprotective mechanisms under in vivo conditions. Measurements on leaves with different amounts of zeaxanthin pointed out that zeaxanthin is necessary for most of the observed nonphotochemical energy quenching, that has to be activated by a transthylakoid ΔpH. An additional sustained energy quenching component was clearly resolved in leaves with high amounts of zeaxanthin. The changes of the Chl fluorescence decay parameters did not correlate with a photoprotective energy dissipation in the reaction centre of photosystem 2 (P680), nor with a ΔpH-mediated, zeaxanthin-independent aggregation of the antenna complexes; no indications for a state 1/state 2 transition of the main light-harvesting complex LHC2 were found.
The antenna sizes of QB-reducing photosystem 2 (PS2) complexes in two different fractions of the subchloroplast particles were compared by measuring time corresponding to the second maximum of the first derivative from induction curve of chlorophyll fluorescence as a function of actinic irradiance. The QB-reducing PS2 complexes in the fraction of particles that originated from inner parts of grana thylakoids had smaller antennae than those in the fraction from non-appressed regions of thylakoid membranes.
Short-term (2 h) treatment with 10 µM abscisic acid decreased stomatal conductance and net photosynthetic rate, and increased carbonic anhydrase activity in pea seedlings. The treatment with 10 µM methyl jasmonate did not significantly affect these parameters. and G. N. Lazova, M. I. Kicheva, L. P. Popova.
Pisum sativum (L.) plants were grown under "white" luminescent lamps, W [45 µ mol(quantum) m-2 s-1] or under the same irradiation supplemented with narrow spectrum red light-emitting diodes (LEDs), RE [λmax = 660 nm, Δλ = 20 nm, 40 µmol(quantum) m-2 s-1]. Significant differences in the chlorophyll (Chl) a fluorescence parameters, degree of State 1-State 2 transition, and the pigment-protein contents were found in plants grown under differing spectral composition. Addition of red LEDs to the "white light" resulted in higher effective quantum yield of photosystem 2 (PS2), i.e. F'v/F'm, linear electron transport (ϕPS2), photochemical quenching (qP), and lower non-photochemical quenching (qN as well as NPQ). The RE plants were characterised by higher degree State 1-State 2 transition, i.e. they were more effective in radiant energy utilisation. Judging from the data of "green" electrophoresis of Chl containing pigment-protein complexes of plants grown under various irradiation qualities, the percentage of Chl in photosystem 2 (PS2) reaction centre complexes in RE plants was higher and there was no difference in the total Chl bound with Chl-proteins of light-harvesting complexes (LHC2). Because the ratio between oligomeric and monomeric LHC2 forms was higher in RE plants, we suggest higher LHC2 stability in these ones. and N. M. Topchyi ... [et al.].
Experiments were performed to distinguish some of the proposed mechanisms by which thylakoid membranes regulate the performance of photosynthetic apparatus in relation to non-photochemical quenching, qN. Aliphatic diamines were used as uncouplers of transmembrane H+ gradient as they can be transported across the membrane at the expense of hydrogen cations. Diamines did not induce changes in low-temperature fluorescence emission but induced different changes in membrane ultrastructure. Positively charged peptides did not affect membrane ultrastructure but blocked qN. In addition, they caused an increase of low temperature fluorescence emission between 710 and 720 nm. For control peptide, the maximal fluorescence increase was found at 715 nm. Fragments of light-harvesting complex 2 in their phosphorylated and non-phosphorylated form shifted the position of this increase. We believe that peptides bind to membrane surface and reduce the mobility of membrane components whose migration is needed for observation of qN. Phosphorylated and non-phosphophorylated LHC2 fragments bind to different binding sites for corresponding forms of the protein. and D. Štys ... [et al.].