Literature DB >> 24408358

Oxygen-evolving system and secondary quinonic acceptors are highly reduced in dark adapted Euglena cells: A thermoluminescence study.

J Farineau1, D Laval-Martin.   

Abstract

Characteristics of thermoluminescence glow curves were compared in three types of Euglena cells: (i) strictly autotrophic, Cramer and Myers cells; (ii) photoheterotrophic cells sampled from an exponentially growing culture containing lactate as substrate repressing the photosynthetic activity; (iii) semiautotrophic cells, sampled when the lactate being totally exhausted, the photosynthesis was enhanced.In autotrophic and semiautotrophic cells, composite curves were observed after series of two or more actinic flashes fired at -10°C, which can be deconvoluted into a large band peaking in the range 12-22°C and a smaller one near 40°C, This second band presents the characteristics of a typical B band (due to S2/3QB (-) recombination), whereas the first one resembled the band, shifted by -15-20°C, which is observed in herbicide resistant plants. The amplitude of this major band, which was in all cases very low after one flash, exhibited oscillations of period four but rapidly damping, with maxima after two and six flashes. In contrast, photoheterotrophic Euglena displayed single, non-oscillating curves with maxima in the range 5-10°C.In autotrophic and semiautotrophic cells, oxidizing pretreatments by either a preillumination with one or more (up to twenty-five) flashes, or a far-red preillumination in the presence of methylviologen, followed by a short dark period, induced thermoluminescence bands almost single and shifted by +3-5°C, or +12°C, respectively. In autotrophic cells, far-red light plus methyl viologen treatment induced a band peaking at 31°C, as in isolated thylakoids from Euglena or higher plants, while it had barely any effect in photoheterotrophic cells.Due to metabolic activities in dark-adapted cells, a reduction of redox groups at the donor and acceptor sides of PS II dark-adapted cells is supposed to occur. Two different explanations can be proposed to explain such a shift in the position of the main band in dark-adapted autotrophic control. The first explanation would be that in these reducing conditions a decreasing value of the equilibrium constant for the reaction: SnQA (-)QB⇌SnQAQB (-), would determine the shift of the main TL band towards low temperatures, as observed in herbicide resistant material. The second explanation would be that the main band would correspond to 'peak III' already observed in vivo and assigned to S2/3QB (2-) recombinations.

Entities:  

Year:  1992        PMID: 24408358     DOI: 10.1007/BF00034793

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


  15 in total

1.  Thermoluminescence studies on spinach leaves and Euglena.

Authors:  T S Desai; P V Sane; V G Tatake
Journal:  Photochem Photobiol       Date:  1975-05       Impact factor: 3.421

Review 2.  Photosystem II, the water-splitting enzyme.

Authors:  A W Rutherford
Journal:  Trends Biochem Sci       Date:  1989-06       Impact factor: 13.807

3.  The reactivation of EPR signal II in chloroplasts treated with reduced dichlorophenol-indophenol: evidence against a dark equilibrium between two oxidation states of the oxygen evolving system.

Authors:  B R Velthuys; J W Visser
Journal:  FEBS Lett       Date:  1975-07-15       Impact factor: 4.124

4.  Charge accumulation and photochemistry in leaves studied by thermoluminescence and delayed light emission.

Authors:  A W Rutherford; Y Inoue
Journal:  Proc Natl Acad Sci U S A       Date:  1984-02       Impact factor: 11.205

5.  Interaction between Chloroplasts and Mitochondria in Microalgae: Role of Glycolysis.

Authors:  F Rebeille; P Gans
Journal:  Plant Physiol       Date:  1988-12       Impact factor: 8.340

6.  Oxygen yield per flash of Chlorella coupled to chemical oxidants under anaerobic conditions.

Authors:  E Greenbaum; D C Mauzerall
Journal:  Photochem Photobiol       Date:  1976-05       Impact factor: 3.421

7.  The effects of low temperature acclimation and photoinhibitory treatments on Photosystem 2 studied by thermoluminescence and fluorescence decay kinetics.

Authors:  J M Briantais; J M Ducruet; M Hodges; G H Krause
Journal:  Photosynth Res       Date:  1992-01       Impact factor: 3.573

8.  Electron paramagnetic resonance signal II in spinach chloroplasts. I. Kinetic analysis for untreated chloroplasts.

Authors:  G T Babcock; K Sauer
Journal:  Biochim Biophys Acta       Date:  1973-12-14

9.  Photosynthetic energy conservation investigated by thermoluminescence. Activation energies and half-lives of thermoluminescence bands of chloroplasts determined by mathematical resolution of glow curves.

Authors:  I Vass; G Horváth; T Herczeg; S Demeter
Journal:  Biochim Biophys Acta       Date:  1981-01-14

10.  Control of misses in oxygen evolution by the oxido-reduction state of plastoquinone in Dunaliella tertiolecta.

Authors:  P C Meunier; R Popovic
Journal:  Photosynth Res       Date:  1990-02       Impact factor: 3.573

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  3 in total

1.  Compared thermoluminescence characteristics of pea thylakoids studied in vitro and in situ (in leaves). The effect of photoinhibitory treatments.

Authors:  J Farineau
Journal:  Photosynth Res       Date:  1993-04       Impact factor: 3.573

2.  The role of transmembrane electrochemical potential and phosphorylation of PS II proteins in temperature induced light emission from ATP-treated lettuce thylakoids.

Authors:  J Farineau
Journal:  Photosynth Res       Date:  1996-03       Impact factor: 3.573

3.  Evolution of PS IIα and PS IIβ centers during the greening of Euglena gracilis Z: Correlations with changes in lipid content.

Authors:  M E Kaoua; D L Laval-Martin
Journal:  Photosynth Res       Date:  1995-02       Impact factor: 3.573

  3 in total

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