The function of chloroplast ferredoxin quinone reductase (FQR)-dependent flow was examined by comparing a wild type tobacco and a tobacco transformant (ΔndhB) in which the ndhB gene had been disrupted with their antimycin A (AA)-fed leaves upon exposure to chilling temperature (4 °C) under low irradiance (100 µmol m-2 s-1 photon flux density). During the chilling stress, the maximum photochemical efficiency of photosystem (PS) 2 (Fv/Fm) decreased markedly in both the controls and AA-fed leaves, and P700+ was also lower in AA-fed leaves than in the controls, implying that FQR-dependent cyclic electron flow around PS1 functioned to protect the photosynthetic apparatus from chilling stress under low irradiance. Under such stress, non-photochemical quenching (NPQ), particularly the fast relaxing NPQ component (qf) and the de-epoxidized ratio of the xanthophyll cycle pigments, (A+Z)/(V+A+Z), formed the difference between AA-fed leaves and controls. The lower NPQ in AA-fed leaves might be related to an inefficient proton gradient across thylakoid membranes (ΔpH) because of inhibiting an FQR-dependent cyclic electron flow around PS1 at chilling temperature under low irradiance. and X.-G. Li ... [et al.].
Ferredoxin (Fd) is a small soluble iron-sulfur protein essential in almost all oxygenic photosynthetic organisms. It contains a single [2Fe-2S] cluster coordinated by four cysteine ligands. It accepts electrons from the stromal surface of PSI and facilitates transfer to a myriad of acceptors involved in diverse metabolic processes, including generation of NADPH via Fd-NADP-reductase, cyclic electron transport for ATP synthesis, nitrate reduction, nitrite reductase, sulfite reduction, hydrogenase and other reductive reactions. Fd serves as the central hub for these diverse cellular reactions and is integral to complex cellular metabolic networks. We describe advances on the central role of Fd and its evolutionary role from cyanobacteria to algae/plants. We compare structural diversity of Fd partners to understand this orchestrating role and shed light on how Fd dynamically partitions between competing partner proteins to enable the optimum transfer of PSI-derived electrons to support cell growth and metabolism., J. Mondal, B. D. Bruce., and Obsahuje bibliografické odkazy
We examined the effects of foliar application of various nitrogen (urea) concentrations on gas-exchange and chlorophyll (Chl) fluorescence characteristics in bean plants treated by heat stress (42/30°C, day/night temperatures). Heat stress caused reductions in contents of Chl a, Chl b, and in maximum photochemical efficiency of PSII by 13, 20, and 27%, respectively, regardless of the N treatment. However, N fertilization caused significant increases in these parameters, especially at higher N concentrations. The net photosynthetic rate and stomatal conductance were enhanced by 32, 60, and 69% and by 25, 88, and 100% due to addition of 5, 10, and 15 mM N, respectively. However, gas-exchange parameters were reduced by 24% due to heat stress. N fertilization alleviated adverse effects of heat stress., I. A. Hassan, H. M. Abou Zeid, W. Taia, N. S. Haiba, A. Zahran, R. H. Badr, R. A. El Dakak, E. A. Shalaby., and Obsahuje bibliografii
In this study, we presented the most commonly employed net photosynthetic light-response curves (PN/I curves) fitted by the Solver function of Microsoft Excel. Excel is attractive not only due to its wide availability as a part of the Microsoft Office suite but also due to the increased level of familiarity of undergraduate students with this tool as opposed to other statistical packages. In this study, we explored the use of Excel as a didactic tool which was built upon a previously published paper presenting an Excel Solver tool for calculation of a net photosynthetic/chloroplastic CO2-response curve. Using the Excel spreadsheets accompanying this paper, researchers and students can quickly and easily choose the best fitted PN/I curve, selecting it by the minimal value of the sum of the squares of the errors. We also criticized the misuse of the asymptotic estimate of the maximum gross photosynthetic rate, the light saturation point estimated at a specific percentile of maximum net photosynthetic rate, and the quantum yield at zero photosynthetic photon flux density and we proposed the replacement of these variables by others more directly linked to plant ecophysiology. and F. de A. Lobo ... [et al.].
We compared flavonoids in green, mature, and senescing flag leaves of wheat grown under ambient (AC - 370 μmol mol-1) and elevated (EC - 550 μmol mol-1) concentrations of CO2 in a FACE (Free Air CO2 Enrichment) system. The concentrations of flag leaf flavonoids (e.g., isoorientin and tricin) decreased to one third in mature leaves, and the majoritary isoorientin almost disappeared in senescing leaves. Flavonoid concentrations increased in green well-developed flag leaves under EC (46 % isoorientin and 55 % tricin), whereas the differences disappeared in mature and senescing flag leaves. Predictions of changes in litter phenolic concentrations and their effects on decomposition rates under EC based on changes in green leaves need to be revised. and J. Peñuelas, M. Estiarte, B. A. Kimball.
Changes in fluorescence emission spectra (293 and 77 K) of phycobilisomes from Nostoc flagelUforme during dissociation in phosphate buffer of various molarity were studied. There were three bands in 77 K fluorescence emission spectra of partly dissociated phycobilisomes: F648, F666 and F686, characteristic of C-phycocyanin (C-PC), allophycocyanin (APC) and allophycocyanin-B (APC-B), respectively. In severely dissociated phycobilisomes, the F666 band was veiy weak, which indicated that linkage between C-PC and APC was severely dissociated, most of the energy trapped by C-PC could not be transferred to APC, but some of it could be transferred directly to APC-B. The phycobiliproteins in these phycobilisomes constitute an energy transfer chain: PEC^C;PC-»APC-»AP^-B. A new model of phycobilisome structure is suggested, in which some C-PC contact directly with APC and others contact with APC-B.