scholarly journals Effects of controlled oxidative stress and uncouplers on primary photosynthetic processes in vegetative cells of Antarctic alga Zygnema sp.

2016 ◽  
Vol 6 (1) ◽  
pp. 96-107 ◽  
Author(s):  
Christos Kakkou ◽  
Miloš Barták ◽  
Josef Hájek ◽  
Kateřina Skácelová ◽  
Jana Hazdrová

In our study, we present responses of Antarctic strain of filamentous alga Zygnema sp. collected at James Ross Island (Antarctica) to application of variuos uncouplers of pri-mary photosynthetic processes. We exposed the alga to different concentrations of nigericin, 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU), dithiothreitol (DTT), methyl viologen (MV) and hydrogen peroxide (H2O2) in order to test stability of photosystem II, involvement of non-photochemical quenching, and PS II functioning under combination of moderate light with particular uncoupler. Oxidative stress tolerance was tested by the combination of hydrogen peroxide (H2O2) and moderate light. Time courses of FV/FM, FPSII, NPQ and qF0 were investigated and particular effects of the above-specified chem-icals discussed. Moderate doses of uncouplers allowing partial recovery, and the doses causing full inhibition of PS II were specified.

2014 ◽  
Vol 4 (1) ◽  
pp. 90-99 ◽  
Author(s):  
Petra Očenášová ◽  
Miloš Barták ◽  
Josef Hájek

The paper focus sensitivity of an Antarctic lichen Usnea antarctica to photoinhibition studied under controlled laboratory conditions. Main emphasis was given to the analysis of quenching mechanisms, i.e. deexcitation pathways of absorbed light energy exploited in non-photochemical processes. Thalli of U. antarctica were collected at the James Ross Island, Antarctica (57°52´57´´ W, 63°48´02´´ S) and transferred in dry state to the Czech Republic. After rewetting in a laboratory, they were exposed to medium light intensities (300, 600 and 1000 mmol m-2 s-1 of photosynthetically active radiation) for 6 h. Before and during photoinhibitory treatments, chlorophyll fluorescence parameters, photoinhibitory (qI), state 1-2 transition (qT), and energy-dependent quenching (qE) in particular were measured to evaluate dose- and time-dependent changes in these parameters. The results showed that among the components forming non-photochemical quenching (qN), qI contributes to the largest extent to qN, while qE and qT contribute less. This finding differs from our earlier studies made in a short term-, and high light-treated U. antarctica that found qE together with qI is the most important part of non-photochemical quenching. Possible explanation is that photoinhibition in PS II in U. ant-arctica, when induced by low to medium light, activates qE to only limited extend and for a relatively short time (tens of minutes). With prolonged high light treatment lasting several hours, qE tends to be reduced to the values close to zero and qI then forms a major part of qN.


2015 ◽  
Vol 6 ◽  
Author(s):  
Mohammad A. Hossain ◽  
Soumen Bhattacharjee ◽  
Saed-Moucheshi Armin ◽  
Pingping Qian ◽  
Wang Xin ◽  
...  

2014 ◽  
Vol 60 (No. 6) ◽  
pp. 274-279 ◽  
Author(s):  
A. Nasraoui-Hajaji ◽  
H. Gouia

N-fertilization type affected differently tomato growth. In the field experiment, hydroponic cultures were conducted using NO<sub>3</sub>-N (5 mmol); mixture of KNO<sub>3</sub>-N (3 mmol) and (NH<sub>4</sub>)<sub>2</sub>SO<sub>4</sub>-N (2 mmol); NH<sub>4</sub><sup>+</sup>-N (5 mmol) or urea&nbsp;(5 mmol) as nitrogen source. Compared to nitrate, ammonium and urea had negative effects on morphology and dry matter production. Effects of the different nitrogen forms were investigated by measuring several photosynthesis parameters and chl a fluorescence. Two different significant types of reaction were found. When nitrogen was added as ammonium or urea, dry weight, chlorophyll tenor, transpiration rate, stomatal conductance and photosynthetic activity were inhibited. Supply of ammonium or urea, reduced the ratio (F<sub>v</sub>/F<sub>m</sub>), photochemical quenching and enhanced the non photochemical quenching. These data suggest that the adverse decrease in tomato growth under ammonium or urea supply may be related principally to inhibition of net photosynthesis activity. The high non photochemical quenching shown in tomato fed with ammonium or urea indicated that PS II was the inhibitory site of NH<sub>4</sub><sup>+</sup>-N which was directly uptaken by roots, or librated via urea hydrolysis cycle.


Biologia ◽  
2017 ◽  
Vol 72 (6) ◽  
Author(s):  
Nuran Durmus ◽  
Abdullah Muhammed Yesilyurt ◽  
Necla Pehlivan ◽  
Sengul Alpay Karaoglu

AbstractAgriculture needs to be sustained by organic processes in current era as population explosion energy and the number of individuals undernourished are raising public concerns. Global warming poses additional threat by lifting the damage of salt stress especially in agro-economically vital crops like maize whose cultivation dates back to Mayans. To that end, cost-effective and organic fungal agents may be great candidates in stress resilience. We isolated the fungal strain from the soil of tea plants and characterized that via 5.8 S rDNA gene with internal transcribed spacer ITS-1 and ITS-2 regions, then named the target strain as TA. Reduced maximum quantum efficiency of PS II (Fv/Fm), the effective quantum yield of PS2 (ΦPS2), electron transport rate (ETR), photochemical quenching (qP) and increased non-photochemical quenching (NPQ) were detected in maize plants stressed with dose dependent salt. Enhanced Fv/Fm, ΦPS2, ETR, qP and decreased NPQ was observed in TA primed plus NaCl treated plants. TA biopriming significantly increased the lengths, fresh and dry weights of root/shoots and decreased the lipid peroxidation. Maize seedlings bioprimed with TA had less MDA and higher soluble protein, proline, total chlorophyll, carotenoid and RWC under NaCl. Furthermore, SOD, GPX and GR activities were much more increased in root and leaves of TA primed seedlings, however CAT activity did not significantly change. This is the first report to our knowledge that TA reverses the damage of NaCl stress on maize growth through improving water status, antioxidant machinery and especially photosynthetic capacity.


2000 ◽  
Vol 355 (1402) ◽  
pp. 1361-1370 ◽  
Author(s):  
Peter Horton ◽  
Alexander V. Ruban ◽  
Mark Wentworth

Non–photochemical quenching of chlorophyll fluorescence (NPQ) is symptomatic of the regulation of energy dissipation by the light–harvesting antenna of photosystem II (PS II). The kinetics of NPQ in both leaves and isolated chloroplasts are determined by the transthylakoid ΔpH and the de–epoxidation state of the xanthophyll cycle. In order to understand the mechanism and regulation of NPQ we have adopted the approaches commonly used in the study of enzyme–catalysed reactions. Steady–state measurements suggest allosteric regulation of NPQ, involving control by the xanthophyll cycle carotenoids of a protonationdependent conformational change that transforms the PS II antenna from an unquenched to a quenched state. The features of this model were confirmed using isolated light–harvesting proteins. Analysis of the rate of induction of quenching both in vitro and in vivo indicated a bimolecular second–order reaction; it is suggested that quenching arises from the reaction between two fluorescent domains, possibly within a single protein subunit. A universal model for this transition is presented based on simple thermodynamic principles governing reaction kinetics.


2016 ◽  
Vol 6 (1) ◽  
pp. 54-65 ◽  
Author(s):  
Michaela Marečková ◽  
Miloš Barták

Chlorophyll fluorescence is an effective tool for investigating characteristics of any photosynthesizing organisms and its responses due to different stressors. Here, we have studied a short-term temperature response on two Antarctic green algal lichen species: Umbilicaria antarctica, and Physconia muscigena. We measured slow chlorophyll fluorescence transients in the species during slow a cooling of thallus temperature from 20°C to 5°C with a 10 min. acclimation at each temperature in dark. The measurements were supplemented with saturation pulses for the analysis of chlorophyll fluorescence parameters: maximum yield of PS II photochemistry (FV/FM), effective quantum yield of PS II photochemistry (FPSII) and non-photochemical quenching (NPQ). In response to decreasing thallus temperature, we observed species-specific changes in chlorophyll fluorescence levels P, S, M, T reached during chlorophyll fluorescence transient as well as in the shape of the chlorophyll fluorescence transients. With a decrease in temperature, the time at which M and T chlorophyll fluorescence levels were reached, increased. These changes were attributed to redox state of plastoquinon pool, changes in Calvin-Benson cycle activity, non-photochemical quenching components, state transition in particular. In this study, we present some chlorophyll fluorescence ratios (P/M, M/T, P/T) and chlorophyll fluorescence increase rates (FR1, i.e. O to P, and FR2 - i.e. S to M) as the parameters reflecting direct temperature effects on chloroplastic apparatus of lichen alga sensitively. We proposed that species-specific changes in the slow phase of chlorophyll fluorescence transients could be potentially used as indicators of low temperature effects in photosynthetic apparatus of lichen algal photobionts. Interspecific differences in response to low temperature might be evaluated using the approach as well.


2000 ◽  
Vol 355 (1402) ◽  
pp. 1405-1418 ◽  
Author(s):  
A. Laisk ◽  
V. Oja

Oxygen yield from single turnover flashes and multiple turnover pulses was measured in sunflower leaves differently pre–illuminated to induce either ‘energy–dependent type’ non–photochemical excitation quenching ( q E ) or reversible, inhibitory type non–photochemical quenching ( q I ). A zirconium O 2 analyser, combined with a flexible gas system, was used for these measurements. Oxygen yield from saturating single turnover flashes was the equivalent of 1.3–2.0 μmol e − m −2 in leaves pre–adapted to low light. It did not decrease when q E quenching was induced by a 1 min exposure to saturating light, but it decreased when pre–illumination was extended to 30–60 min. Oxygen evolution from saturating multiple turnover pulses behaved similarly: it did not decrease with the rapidly induced q E but decreased considerably when exposure to saturating light was extended or O 2 concentration was decreased to 0.4%. Parallel recording of chlorophyll fluorescence and O 2 evolution during multiple turnover pulses, interpreted with the help of a mathematical model of photosystem II (PS II) electron transport, revealed PS II donor and acceptor side resistances. These experiments showed that PS II properties depend on the type of non–photochemical quenching present. The rapidly induced and rapidly reversible q E type (photoprotective) quenching does not induce changes in the number of active PS II or in the PS II maximum turnover rate, thus confirming the antenna mechanism of q E. The more slowly induced but still reversible q I type quenching (photoinactivation) induced a decrease in the number of active PS II and in the maximum PS II turnover rate. Modelling showed that, mainly, the acceptor side resistance of PS II increased in parallel with the reversible q I. Oxygen yield from single turnover flashes and multiple turnover pulses was measured in sunflower leaves differently pre–illuminated to induce either ‘energy–dependent type’ non–photochemical excitation quenching ( q E ) or reversible, inhibitory type non–photochemical quenching ( q I ). A zirconium O 2 analyser, combined with a flexible gas system, was used for these measurements. Oxygen yield from saturating single turnover flashes was the equivalent of 1.3–2.0 μmol e − m −2 in leaves pre–adapted to low light. It did not decrease when q E quenching was induced by a 1 min exposure to saturating light, but it decreased when pre–illumination was extended to 30–60 min. Oxygen evolution from saturating multiple turnover pulses behaved similarly: it did not decrease with the rapidly induced q E but decreased considerably when exposure to saturating light was extended or O 2 concentration was decreased to 0.4%. Parallel recording of chlorophyll fluorescence and O 2 evolution during multiple turnover pulses, interpreted with the help of a mathematical model of photosystem II (PS II) electron transport, revealed PS II donor and acceptor side resistances. These experiments showed that PS II properties depend on the type of non–photochemical quenching present. The rapidly induced and rapidly reversible q E type (photoprotective) quenching does not induce changes in the number of active PS II or in the PS II maximum turnover rate, thus confirming the antenna mechanism of q E. The more slowly induced but still reversible q I type quenching (photoinactivation) induced a decrease in the number of active PS II and in the maximum PS II turnover rate. Modelling showed that, mainly, the acceptor side resistance of PS II increased in parallel with the reversible q I.


2000 ◽  
Vol 355 (1402) ◽  
pp. 1337-1344 ◽  
Author(s):  
Jon Nield ◽  
Christiane Funk ◽  
James Barber

This paper addresses the question of whether the PsbS protein of photosystem two (PS II) is located within the LHC II–PS II supercomplex for which a three–dimensional structure has been obtained by cryoelectron microscopy and single particle analysis. The PsbS protein has recently been implicated as the site for non–photochemical quenching. Based both on immunoblotting analyses and structural considerations of an improved model of the spinach LHC II–PS II supercomplex, we conclude that the PsbS protein is not located within the supercomplex. Analyses of other fractions resulting from the solubilization of PS II–enriched membranes derived from spinach suggest that the PsbS protein is located in the LHC II–rich regions that interconnect the supercomplex within the membrane.


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