Literature DB >> 16228309

Photoinactivation of the photosynthetic electron transport chain by accumulation of over-saturating light pulses given to dark adapted pea leaves.

S Apostol1, J M Briantais, N Moise, Z G Cerovic, I Moya.   

Abstract

The effect of cumulative over-saturating pulses (OSP) of white light (1 s, >10 000 mumol photons m(-2) s(-1)), applied every 20 min on pea leaves, was investigated during a complete diurnal cycle of 24 h. In dark-adapted leaves, this treatment leads to a progressive decline of the optimum Photosystem II (PS II) quantum yield. Continuous low background light (except far-red light) had a protective effect against this OSP-induced photoinactivation. The lack of far-red effect could be due to its absorption mainly in PS I and not in PS II, but could be also due to the general low absorption in this wavelength region. The photoinactivation was enhanced in leaves that had been previously infiltrated with chloramphenicol. The quantum yield of CO(2) assimilation, but not its maximal capacity, was inhibited by the OSP treatment. The most spectacular effects observed, in addition to an irreversible quenching of Fm, was a strong inhibition of Q(A) (-) reoxidation revealed by a large increase in the Fs level and consequently by a decrease of DeltaF/Fm'. Under such conditions, we observed that the electron flow deduced from DeltaF/Fm' underestimated the real electron flow to CO(2). Time-resolved Chlorophyll a fluorescence measurements showed that the reduced capacity of Q(A) (-) reoxidation in OSP treated leaves was accompanied by the appearance of a 4.7 ns component attributed to PS II charge recombination. We suggest that a modification at the Q(B) site may influence the redox potential of Q(A)/Q(A) (-), facilitating the reversion of the primary charge separation. In addition, a 1.2 ns fluorescence component accumulated, which appeared to be responsible for the underestimation of PS II electron flow. The observed photoinactivation seemed to be different from the photoinhibition often described in the literature, which occurs under continuous light.

Entities:  

Year:  2001        PMID: 16228309     DOI: 10.1023/A:1010676618028

Source DB:  PubMed          Journal:  Photosynth Res        ISSN: 0166-8595            Impact factor:   3.573


  24 in total

Review 1.  Too much of a good thing: light can be bad for photosynthesis.

Authors:  J Barber; B Andersson
Journal:  Trends Biochem Sci       Date:  1992-02       Impact factor: 13.807

2.  Control of Photosystem II in spinach leaves by continuous light and by light pulses given in the dark.

Authors:  N G Bukhov; C Wiese; S Neimanis; U Heber
Journal:  Photosynth Res       Date:  1996-11       Impact factor: 3.573

3.  Heat stress induces in leaves an increase of the minimum level of chlorophyll fluorescence, Fo: A time-resolved analysis.

Authors:  J M Briantais; J Dacosta; Y Goulas; J M Ducruet; I Moya
Journal:  Photosynth Res       Date:  1996-05       Impact factor: 3.573

4.  Photosystem II chlorophyll a fluorescence lifetimes and intensity are independent of the antenna size differences between barley wild-type and chlorina mutants: Photochemical quenching and xanthophyll cycle-dependent nonphotochemical quenching of fluorescence.

Authors:  A M Gilmore; T L Hazlett; P G Debrunner
Journal:  Photosynth Res       Date:  1996-05       Impact factor: 3.573

5.  Fractional control of photosynthesis by the QB protein, the cytochrome f/b 6 complex and other components of the photosynthesic apparatus.

Authors:  U Heber; S Neimanis; K J Dietz
Journal:  Planta       Date:  1988-02       Impact factor: 4.116

6.  Functioning of photosystems I and II in pea leaves exposed to heat stress in the presence or absence of light : Analysis using in-vivo fluorescence, absorbance, oxygen and photoacoustic measurements.

Authors:  M Havaux; H Greppin; R J Strasser
Journal:  Planta       Date:  1991-12       Impact factor: 4.116

7.  The effect of decreasing temperature up to chilling values on the in vivo F685/F735 chlorophyll fluorescence ratio in Phaseolus vulgaris and Pisum sativum: the role of the photosystem I contribution to the 735 nm fluorescence band.

Authors:  G Agati; Z G Cerovic; I Moya
Journal:  Photochem Photobiol       Date:  2000-07       Impact factor: 3.421

8.  Global spectral-kinetic analysis of room temperature chlorophyll a fluorescence from light-harvesting antenna mutants of barley.

Authors:  A M Gilmor; S Itoh
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2000-10-29       Impact factor: 6.237

9.  Comparative time-resolved photosystem II chlorophyll a fluorescence analyses reveal distinctive differences between photoinhibitory reaction center damage and xanthophyll cycle-dependent energy dissipation.

Authors:  A M Gilmore; T L Hazlett; P G Debrunner
Journal:  Photochem Photobiol       Date:  1996-09       Impact factor: 3.421

10.  Photoinhibition of photosynthesis in intact bean leaves: role of light and temperature, and requirement for chloroplast-protein synthesis during recovery.

Authors:  D H Greer; J A Berry; O Björkman
Journal:  Planta       Date:  1986-06       Impact factor: 4.116

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  2 in total

1.  Iron deficiency interrupts energy transfer from a disconnected part of the antenna to the rest of Photosystem II.

Authors:  F Morales; N Moise; R Quílez; A Abadía; J Abadía; I Moya
Journal:  Photosynth Res       Date:  2001       Impact factor: 3.573

2.  Repetitive light pulse-induced photoinhibition of photosystem I severely affects CO2 assimilation and photoprotection in wheat leaves.

Authors:  Marek Zivcak; Marian Brestic; Kristyna Kunderlikova; Oksana Sytar; Suleyman I Allakhverdiev
Journal:  Photosynth Res       Date:  2015-04-01       Impact factor: 3.573

  2 in total

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