scholarly journals Dark recovery of the Chl a fluorescence transient (OJIP) after light adaptation: The qT-component of non-photochemical quenching is related to an activated photosystem I acceptor side

2006 ◽  
Vol 1757 (7) ◽  
pp. 787-797 ◽  
Author(s):  
Gert Schansker ◽  
Szilvia Z. Tóth ◽  
Reto J. Strasser
2002 ◽  
Vol 29 (10) ◽  
pp. 1141 ◽  
Author(s):  
Govindjee ◽  
Manfredo J. Seufferheld

This paper deals first with the early, although incomplete, history of photoinhibition, of 'non-QA-related chlorophyll (Chl) a fluorescence changes', and the xanthophyll cycle that preceded the discovery of the correlation between non-photochemical quenching of Chl a fluorescence (NPQ) and conversion of violaxanthin to zeaxanthin. It includes the crucial observation that the fluorescence intensity quenching, when plants are exposed to excess light, is indeed due to a change in the quantum yield of fluorescence. The history ends with a novel turn in the direction of research — isolation and characterization of NPQ xanthophyll-cycle mutants of Chlamydomonas reinhardtii Dangeard and Arabidopsis thaliana (L.) Heynh., blocked in conversion of violaxanthin to zeaxanthin, and zeaxanthin to violaxanthin, respectively. In the second part of the paper, we extend the characterization of two of these mutants (npq1, which accumulates violaxanthin, and npq2, which accumulates zeaxanthin) through parallel measurements on growth, and several assays of PSII function: oxygen evolution, Chl a fluorescence transient (the Kautsky effect), the two-electron gate function of PSII, the back reactions around PSII, and measurements of NPQ by pulse-amplitude modulation (PAM 2000) fluorimeter. We show that, in the npq2 mutant, Chl a fluorescence is quenched both in the absence and presence of 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU). However, no differences are observed in functioning of the electron-acceptor side of PSII — both the two-electron gate and the back reactions are unchanged. In addition, the role of protons in fluorescence quenching during the 'P-to-S' fluorescence transient was confirmed by the effect of nigericin in decreasing this quenching effect. Also, the absence of zeaxanthin in the npq1 mutant leads to reduced oxygen evolution at high light intensity, suggesting another protective role of this carotenoid. The available data not only support the current model of NPQ that includes roles for both pH and the xanthophylls, but also are consistent with additional protective roles of zeaxanthin. However, this paper emphasizes that we still lack sufficient understanding of the different parts of NPQ, and that the precise mechanisms of photoprotection in the alga Chlamydomonas may not be the same as those in higher plants.


2002 ◽  
Vol 29 (4) ◽  
pp. 425 ◽  
Author(s):  
Govindjee ◽  
Paul Spilotro

A major photoprotective mechanism that plants employ against excess light involves interplay between the xanthophyll cycle and the accumulation of protons. Using mutants in the xanthophyll cycle, the roles of violaxanthin, antheraxanthin and zeaxanthin have already been well established. In this paper, we present data on intact leaves of a mutant [coupling factor quick recovery mutant (cfq); atpC1:E244K] of Arabidopsis thaliana that we expected, based on 515-nm absorbance changes (Gabrys et al. 1994, Plant Physiology 104, 769–776), to have differences in light-induced ΔpH. The significance of this paper is: (i) it is the first study of the photoprotective energy dissipation involving a mutant of the pH gradient; it establishes that protons play an important role in the pattern of non-photochemical quenching (NPQ) of chlorophyll (Chl) a fluorescence; and (ii) differences between the cfq and the wild type (wt) are observed only under subsaturating light intensities, and are strongest in the initial few minutes of the induction period. Our results on light-intensity dependent Chl* a fluorescence transients (the Kautsky effect), and on NPQ of Chl a fluorescence, at 50–250 μmol photons m–2 s–1 demonstrate: (i) the ‘P-to-S’ (or ‘T’) decay, known to be related to [H+] (Briantais et al. 1979, Biochimica et Biophysica Acta 548, 128–138), is slowed in the mutant; and (ii) the pattern of NPQ kinetics is different in the initial 100 s — in the wt leaves, there is a marked rise and decline, and in the cfq mutant, there is a slowed rise. These differences are absent at 750 μmol photons m–2 s–1. Pre-illumination and nigericin (an uncoupler that dissipates the proton gradient) treatment of the cfq mutant, which has lower ΔpH relative to wild type, confirm the conclusion that protons play an important role in the quenching of Chl a fluorescence.


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.


2015 ◽  
Vol 105 (2) ◽  
pp. 180-188 ◽  
Author(s):  
Sandro Dan Tatagiba ◽  
Fábio Murilo DaMatta ◽  
Fabrício Ávila Rodrigues

This study was intended to analyze the photosynthetic performance of rice leaf blades infected with Monographella albescens by combining chlorophyll (Chl) a fluorescence images with gas exchange and photosynthetic pigment pools. The net CO2 assimilation rate, stomatal conductance, transpiration rate, total Chl and carotenoid pools, and Chl a/b ratio all decreased but the internal CO2 concentration increased in the inoculated plants compared with their noninoculated counterparts. The first detectable changes in the images of Chl a fluorescence from the leaves of inoculated plants were already evident at 24 h after inoculation (hai) and increased dramatically as the leaf scald lesions expanded. However, these changes were negligible for the photosystem II photochemical efficiency (Fv/Fm) at 24 hai, in contrast to other Chl fluorescence traits such as the photochemical quenching coefficient, yield of photochemistry, and yield for dissipation by downregulation; which, therefore, were much more sensitive than the Fv/Fm ratio in assessing the early stages of fungal infection. It was also demonstrated that M. albescens was able to impair the photosynthetic process in both symptomatic and asymptomatic leaf areas. Overall, it was proven that Chl a fluorescence imaging is an excellent tool to describe the loss of functionality of the photosynthetic apparatus occurring in rice leaves upon infection by M. albescens.


2021 ◽  
Vol 25 (02) ◽  
pp. 338-344
Author(s):  
Zengbing Liu

Bacterial leaf blight (BLB) caused by Xanthomonas oryzae pv. oryzae is a serious disease affecting rice. Understanding of the effects of this disease on photosynthesis and chlorophyll (Chl) a fluorescence is important in rice management. We studied the effect of BLB on enzyme activities, photosynthetic rate (Pn) and Chl a fluorescence transient in susceptible Neiwuyou 8015 and resistant Shenzhou 98 rice cultivars. BLB had a negative effect on rice net photosynthesis (Pn) and stomatal conductance (Gs). Superoxide dismutase (SOD), polyphenol oxidase (PPO), phenylalanine ammonia lyase (PAL) activities, malondialdehyde (MDA) contents were increased while Chl content was decreased, indicating that rice photosynthetic functions were damaged by BLB. The effect of BLB on photosynthesis was greater in susceptible rice than in resistant rice. A significant difference of Chl a fluorescence transient curves was observed between BLB treatments and healthy ones. Parameters measured in transient rice Chl a fluorescence showed the photosynthetic reaction center was inactive after BLB. These findings will help in evaluating rice resistance and may be useful for rice disease management. © 2021 Friends Science Publishers


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.


2005 ◽  
Vol 280 (23) ◽  
pp. 22191-22197 ◽  
Author(s):  
Tamaki Fujimori ◽  
Yukako Hihara ◽  
Kintake Sonoike

To avoid the photodamage, cyanobacteria regulate the distribution of light energy absorbed by phycobilisome antenna either to photosystem II or to photosystem I (PSI) upon high light acclimation by the process so-called state transition. We found that an alternative PSI subunit, PsaK2 (sll0629 gene product), is involved in this process in the cyanobacterium Synechocystis sp. PCC 6803. An examination of the subunit composition of the purified PSI reaction center complexes revealed that PsaK2 subunit was absent in the PSI complexes under low light condition, but was incorporated into the complexes during acclimation to high light. The growth of the psaK2 mutant on solid medium was inhibited under high light condition. We determined the photosynthetic characteristics of the wild type strain and the two mutants, the psaK1 (ssr0390) mutant and the psaK2 mutant, using pulse amplitude modulation fluorometer. Non-photochemical quenching, which reflects the energy transfer from phycobilisome to PSI in cyanobacteria, was higher in high light grown cells than in low light grown cells, both in the wild type and the psaK1 mutant. However, this change of non-photochemical quenching during acclimation to high light was not observed in the psaK2 mutant. Thus, PsaK2 subunit is involved in the energy transfer from phycobilisome to PSI under high light condition. The role of PsaK2 in state transition under high light condition was also confirmed by chlorophyll fluorescence emission spectra determined at 77 K. The results suggest that PsaK2-dependent state transition is essential for the growth of this cyanobacterium under high light condition.


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