In order to quantify the effects of thinning on photosynthetic parameters and associated change in leaf nitrogen (N) contents, half of the trees in a 10-year-old Chamaecyparis obtusa (Sieb. et Zucc.) Endl. stand (36° 3'N, 140°7'E) were removed, giving a final density of 1 500 trees ha-1, in May 2004. Photosynthetic photon flux density (PPFD) and leaf N and carbon (C) contents in the lower (L), middle (M), and upper (U) crowns were monitored one, three, and five months after thinning in both the thinned stand and a non-thinned control stand. In addition, leaves' photosynthetic responses to CO2 concentration were simultaneously measured in situ to estimate the maximum rates of carboxylation (Vcmax) and electron transport (Jmax). Thinning increased PPFD in the L and M crowns but not in the U crown. Vcmax in both the L and M crowns of the thinned stand increased significantly in comparison with the same crown position of the control stand in the three and five months following thinning. In addition, the thinned stand exhibited an increase in N partitioned to ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBPCO) in the L and M crowns relative to the control stand three and five months after thinning, indicating that N had been redistributed within the photosynthetic machinery. Thinning did not affect N per unit area at any of the crown positions, but significantly increased the content of N as a fraction of the total leaf dry mass in the L and M crowns three and five months after thinning. This was a consequence of a decrease in leaf dry mass due to rapid shoot growth. Thus thinning did not cause a redistribution of N between leaves. Thinning improved irradiance in the L and M crowns of C. obtusa, leading to photosynthetic acclimation. Photosynthetic acclimation in the first year mainly occurred via redistribution of N within but not between leaves. and Q. Han, M. Araki, Y. Chiba.
In this article, the effects of increased light intensities on antioxidant metabolism during ex vitro establishment of Ulmus minor micropropagated plants are investigated. Three month old in vitro plants were acclimatized to ex vitro conditions in a climate chamber with two different light intensities, 200 μmol m-2 s-1 (high light, HL) and 100 μmol m-2 s-1 (low light, LL) during 40 days. Immediately after ex vitro transfer, the increase of both malondialdehyde (MDA) and electrolyte leakage in persistent leaves is indicative of oxidative stress. As the acclimatization continues, an upregulation of the superoxide dismutase (SOD), catalase (CAT), and glutathione reductase (GR) enzyme activities were also observed. Simultaneously, MDA content and membrane permeability stabilized, suggesting that the antioxidant enzymes decrease the deleterious effects of reactive oxygen species (ROS) generation. Unexpectedly, newly formed leaves presented a different pattern of antioxidative profile, with high levels of MDA and membrane leakage and low antioxidant enzyme activity. Despite these differences, both leaf types looked healthy (e.g. greenish, with no necrotic spots) during the whole acclimatization period. The results indicate that micropropagated U. minor plantlets develop an antioxidant enzyme system after ex vitro transfer and that, in general, LL treatment leads to lower oxidative stress. Moreover, new leaves tolerate higher levels of ROS without the need to activate the antioxidative pathway, which suggests that the environment at which leaves are exposed during its formation determinate their ability to tolerate ROS. and M. C. Dias, G. Pinto, C. Santos.
European larch (Larix decidua Mill.) and Norway spruce [Picea abies (L.) Karst.] synthesize chlorophyll (Chl) in darkness. This paper compares Chl accumulation in 14-d-old dark-grown seedlings of L. decidua and P. abies after shortterm (24 h) feeding with 5-aminolevulinic acid (ALA). We used two ALA concentrations (1 and 10 mM) fed to cotyledons of both species in darkness and in continuous light. The dark-grown seedlings of L. decidua accumulated Chl only in trace amounts and the seedlings remained etiolated. In contrast, P. abies seedlings grown in darkness were green and had significantly higher Chl content. After ALA feeding, higher protochlorophyllide (Pchlide) content was observed in L. decidua than in P. abies cotyledons incubated in darkness. Although short-term ALA feeding stimulated the synthesis of Pchlide, Chl content did not change significantly in cotyledons incubated in darkness. The Chl accumulation in cotyledons fed with ALA was similar to the rate of Chl accumulation in the controls. Higher Chl accumulation was reported in control samples after illumination: 86.9% in L. decidua cotyledons and 46.4% in P. abies cotyledons. The Chl content decreased and bleaching occurred in cotyledons incubated with ALA in light due to photooxidation. Analyses of Chlbinding proteins (D1 and LHCIIb) by Western blotting proved differences between Chl biosynthesis in L. decidua and P. abies seedlings in the dark and in the light. No remarkable increase was found in protein accumulation (D1 and LHCIIb) after ALA application. Our results showed interspecific difference in Chl synthesis between two gymnosperms. Shortterm ALA feeding did not stimulate Chl synthesis, thus ALA synthesis was not the rate-limiting step in Chl synthesis in the dark., N. Maximová, Ľ. Slováková., and Obsahuje bibliografii
An acid pH in the lumen of chloroplast thylakoids is necessary in order to derive the required amount of CO2 to account for the observed rates of carbon fixation. We point out that the endosymbiotic derivation of the chloroplast from a cyanobacterium would have resulted in the lumen of the thylakoid having an acid pH. The thylakoids of cyanobacteria are continuous with the plasma membrane, resulting in the lumen of the thylakoid being open to the outside of the cell. Endosymbiosis resulted in the cyanobacterium being taken up into a food vacuole of a protozoan. The vacuole would have had an acid pH, probably around pH 5, so the endosymbiotic bacterium would have been surrounded by an environment with an acidic pH. The lumen of the thylakoids would have been at an acid pH since they were open to the exterior of the cell, and to the contents of the vacuole. and R. E. Lee, P. Kugrens.
In chloroplasts of Spinacea oleracea L., Hg2+ ions interact with some sites in the photosynthetic electron transport chain: (l) with the intermediates Z+/D+ situated in the D1 and D2 proteins and with the manganese cluster in the oxygen evolving complex which are located on the donor side of photosystem (PS) 2, (2) with the chlorophyll a dimer in the core of PS1 (P700). P700 is oxidized in the dark by HgCl2. The Hg2+ ions form organometallic complexes with amino acids contained in chloroplast proteins. and F. Šeršeň, K. Král'ová, A. Bumbálová.
The effect of 30 % defoliation of shaded leaves in lower layers of plant was studied on activities of carbonic anhydrase (CA) and ribulose-1,5-bisphosphate carboxylase (RuBPC), leaf dry mass per unit leaf area, and plant dry mass of mustard (Brassica juncea). Removal of 30 % of leaves resulted in increased CA and RuBPC activities of leaves, and leaf and plant dry masses.
In order to study photosynthetic characteristics, phosphoenolpyruvate carboxylase (PEPC) and ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBPCO) activities as well as soluble protein and chlorophyll contents were determined in leaf and fruit pericarp samples from diverse coffee genotypes (Coffea arabica cv. Colombia, Caturra, Caturra Erecta, San Pacho, Tipica, C. stenophylla, C. eugenioides, C. congensis, C. canephora, C. canephora cv. Arabusta, C. arabica cv. Caturra×C. canephora and Hibrido de Timor. We found a slightly higher PEPC activity in fruit pericarp than in leaves, while RuBPCO activity was much lower in pericarp than leaf tissue. Partial purification of PEPC and RuBPCO was carried out from leaves of C. arabica cv. Caturra and Michaelis-Menten kinetics for RuBPCO (Km CO2 = 5.34 µM), (Km RuBP = 9.09 µM) and PEPC (Km PEP = 19.5 µM) were determined. Leaf tissues of Colombia, Hibrido de Timor, and Caturra consistently showed higher content of protein [55.4-64.4 g kg-1 (f.m.)] than San Pacho, C. stenophylla, Tipica, Caturra Erecta, and Caturra×C. canephora [25.6-36.9 g kg-1 (f.m.)] and C. canephora cv. Arabusta, Borbon, C. congensis, C. eugenioides, and C. canephora [16.1-21.1 g kg-1 (f.m.)]. and Y. Lopez ... [et al.].
The pattern of activity of 1-aminocyclopropane carboxylic acid synthase (ACS) was similar to photosynthetic and growth traits observed at 30, 45, and 60 d after sowing in mustard (Brassica juncea L.) cultivars Varuna and RH 30 differing in photosynthetic capacity. Higher activity of ACS and therefore ethylene release in Varuna than RH 30 increased stomatal conductance, intercellular CO2 concentration, carboxylation rate (carbonic anhydrase and intrinsic water use efficiency), and thus net photosynthetic rate (PN) and leaf and plant dry masses (DM) at all sampling times. Moreover, Varuna also had larger leaf area which contributed to higher PN and DM. A positive correlation between ACS activity and PN and leaf area was found in both the cultivars. Thus ACS activity may affect PN through ethylene-induced changes on foliar gas exchange and leaf growth.
The activity of enzymes characteristic for C4-type photosynthesis was determined in different organs of two herbaceous plants: Reynoutria japonica Houtt. and Helianthus tuberosus L. The activity of phosphoenolpyruvate carboxylase (PEPC) was usually higher in the roots, some of the stem tissues and petioles in comparison to the leaf blades. The highest activity of malic enzymes (NAD-ME, NADP-ME) and phosphoenolpyruvate carboxykinase (PEPCK) was in the petioles and stem tissues of both plants and the lowest in the leaf blades and the pith of Helianthus tuberosus L. and M. Kocurek, J. Pilarski.
The impact of heat shock on minimising the activity of photosystem 2 (PS2) initiating high lipid peroxidation (POL) level and consequently changes in the enzymatic-antioxidant protective system was studied in seedlings of two Egyptian cultivars of barley (Giza 124 and 125). Heat doses (35 and 45 °C for 2, 4, 6, and 8 h) decreased chlorophyll (Chl) contents coupled with an increase in Chl a/b ratio, diminished Hill reaction activity, and quenched Chl a fluorescence emission spectra. These parameters reflect the disturbance of the structure, composition, and function of the photosynthetic apparatus as well as the activity of PS2. POL level, as dependent on the balance between pro- and anti-oxidant systems, was directly correlated with temperature, exposure time, and their interaction. Heat shock caused an increase in the electric conductivity of cell membrane, and malonyldialdehyde content (a peroxidation product) coupled with the disappearance of the polyunsaturated linolenic acid (C18:3), reflecting the peroxidation of membrane lipids which led to the loss of membrane selective permeability. Moreover, it induced distinct and significant changes in activities of antioxidant enzymes. Superoxide dismutase and peroxidase activities have been progressively enhanced by moderate and elevated heat doses, but the most elevated one (45 °C for 8 h) showed a decrease in activities of both enzymes. In contrast, catalase activity was reduced with all heat shocks. and F. El-Shintinawy ... [et al.].