scholarly journals Alteration of photosystem II properties with non-photochemical excitation quenching

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.

1987 ◽  
Vol 42 (6) ◽  
pp. 698-703 ◽  
Author(s):  
Gernot Renger ◽  
Angela Kayed ◽  
Walter Oettmeier

The interaction of halogenated p-benzoquinones with PS II has been analyzed by measurements of fluorescence induction curves and the average oxygen yield per flash in isolated class II chloroplasts. It was found: 1)The normalized area over the fluorescence induction curve in the presence of DCMU. A/Fmax, markedly increases if halogenated p-benzoquinones are added before DCMU. The effect is eliminated by DCMU addition prior to that of the quinones. 2)The extent of A/Fmax increases with increasing dark time between the additions of 2,3.5-tri- bromo-6-methyl-1,4-benzoquinone (TBTO) and DCMU. respectively. 3) Some of the halogenated p-benzoquinones were found to act as efficient electron acceptors under repetitive excitation at low flash frequency (2 Hz). In the case of TBTO and 2,3-di-chloro-5-t-butyl-1,4-benzoquinone (TBU 13) the sensitivity of the average oxygen yield per flash was shifted towards higher concentrations of DCMU. 4) Halogenated p-benzoquinones can also affect the stability of oxidizing redox equivalents in the water oxidizing enzyme system Y. This effect depends on the nature of the substituents. The present results are interpreted by the assumption of a covalent binding of halogenated p-benzoquinones in the vicinity of Qᴀ. This binding is prevented by DCMU. The possibility of allosteric interaction between the donor and acceptor side of PS II is discussed.


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.


Plants ◽  
2020 ◽  
Vol 9 (3) ◽  
pp. 316 ◽  
Author(s):  
Elias Kaiser ◽  
Dirk Walther ◽  
Ute Armbruster

The capacity of photoautotrophs to fix carbon depends on the efficiency of the conversion of light energy into chemical potential by photosynthesis. In nature, light input into photosynthesis can change very rapidly and dramatically. To analyze how genetic variation in Arabidopsis thaliana affects photosynthesis and growth under dynamic light conditions, 36 randomly chosen natural accessions were grown under uniform and fluctuating light intensities. After 14 days of growth under uniform or fluctuating light regimes, maximum photosystem II quantum efficiency (Fv/Fm) was determined, photosystem II operating efficiency (ΦPSII) and non-photochemical quenching (NPQ) were measured in low light, and projected leaf area (PLA) as well as the number of visible leaves were estimated. Our data show that ΦPSII and PLA were decreased and NPQ was increased, while Fv/Fm and number of visible leaves were unaffected, in most accessions grown under fluctuating compared to uniform light. There were large changes between accessions for most of these parameters, which, however, were not correlated with genomic variation. Fast growing accessions under uniform light showed the largest growth reductions under fluctuating light, which correlated strongly with a reduction in ΦPSII, suggesting that, under fluctuating light, photosynthesis controls growth and not vice versa.


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.


1999 ◽  
Vol 26 (3) ◽  
pp. 283 ◽  
Author(s):  
Congming Lu ◽  
Giuseppe Torzillo ◽  
Avigad Vonshak

The kinetic response of photosystem II (PS II) photochemistry in Spirulina platensis(Norstedt M2 ) to high salinity (0.75 M NaCl) was found to consist of two phases. The first phase, which was independent of light, was characterized by a rapid decrease (15–50%) in the maximal efficiency of PS II photochemistry (Fv /Fm), the efficiency of excitation energy capture by open PS II reaction centres (Fv′/Fm′), photochemical quenching (qp) and the quantum yield of PS II electron transport (Φ PS II) in the first 15 min, followed by a recovery up to about 80–92% of their initial levels within the next 2 h. The second phase took place after 4 h, in which further decline in above parameters occurred. Such a decline occurred only when the cells were incubated in the light, reaching levels as low as 45–70% of their initial levels after 12 h. At the same time, non-photochemical quenching (qN) and Q B -non-reducing PS II reaction centres increased significantly in the first 15 min and then recovered to the initial level during the first phase but increased again in the light in the second phase. The changes in the probability of electron transfer beyond QA (ψo) and the yield of electron transport beyond QA (φ Eo), the absorption flux (ABS/RC) and the trapping flux (TRo /RC) per PS II reaction centre also displayed two different phases. The causes responsible for the decreased quantum yield of PS II electron transport during the two phases are discussed.


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