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pH dependent chlorophyll fluorescence quenching in spinach thylakoids from light treated or dark adapted leaves

Abstract

The pH dependence of maximum chlorophyll fluorescence yield (Fm) was examined in spinach thylakoids in the presence of nigericin to dissipate the transthylakoid pH gradient. 3-(3′,4′-dichlorophenyl)-1,1-dimethylurea (DCMU) was present to eliminate photochemical quenching. Thylakoids were prepared from dark adapted leaves (‘dark’ thylakoids) or preilluminated leaves (‘light’ thylakoids). In the latter there had been approximately 50% conversion of the xanthophyll violaxanthin to zeaxanthin, while no conversion had occurred in the former. In the presence of a reductant such as ascorbate, antimycin A sensitive quenching was observed (half maximal quenching at 5 μM), whose pH dependence differed between the two types of thylakoid. Preillumination of leaves resulted in more quenching at pH values where very little quenching was observed in ‘dark’ thylakoids (pH 5–7.6). This was similar to activation of high-energy-state quenching (qE) observed previously (Rees D, Young A, Noctor G, Britton G and Horton P (1989) FEBS Lett 256: 85–90). Thylakoids isolated from preilluminated DTT treated leaves, that contained no zeaxanthin, behaved like dark thylakoids. A second form of quenching was observed in the presence of ferricyanide, that could be reversed by the addition of ascorbate. This was not antimycin A sensitive and showed the same pH dependence in both types of thylakoid. The former type of quenching, but not the latter, showed similar low temperature fluorescence emission spectra to qE, and was considered to occur by the same mechanism.

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Abbreviations

DCMU:

3(3′,4′-dichlorophenyl)-1,1-dimethylurea

DTT:

dithiothreitol

EDTA:

Ethylenediaminetetra-acetic acid

F0 :

dark level fluorescence yield

Fm :

maximum fluorescence yield

Fv/Fm :

ratio of variable to total fluorescence yield

Hepes:

4-(2-hydroxyethyl)1-piperazineethanesul-phonic acid

Mes:

2-(N-morpholino) ethanesulfonate

pH:

transthylakoid pH gradient

PS I:

Photosystem I

PS II:

Photosystem II

QA :

primary stable electron acceptor of Photosystem II

qE:

high-energy-state fluorescence quenching

References

  • AdamsIII WW, Demmig-Adams B and Winter K (1990) Relative contributions of zeaxanthin-related and zeaxanthin-unrelated types of ‘high-energy-state’ quenching of chlorophyll fluorescence in spinach leaves exposed to various environmental conditions. Plant Physiol 92: 302–309

    Google Scholar 

  • Barry P, Young AJ and Britton G (1990) Photodestruction of pigments in higher plants by herbicide action. I. The effect of DCMU (diuron) on isolated chloroplasts. J Exp Bot 41: 123–129

    Google Scholar 

  • Bilger W, Björkman O and Thayer SS (1989) Light-induced spectral absorbance changes in relation to photosynthesis and the epoxidation state of xanthophyll cycle components in cotton leaves. Plant Physiol 91: 542–551

    Google Scholar 

  • Briantais JM, Vernotte C, Picaud M and Krause GH (1979) A quantitative study of the slow decline of chlorophyll-a fluorescence in isolated chloroplasts. Biochim Biophys Acta 548: 128–138

    Google Scholar 

  • Crofts J and Horton P (1991) Dissipation of excitation energy by Photosystem 2 particles at low pH. Biochim Biophys Acta 1058: 187–193

    Google Scholar 

  • Demmig B, Winter K, Kruger A and Czygan F-C (1987) Photoinhibition and zeaxanthin formation in intact leaves. A possible role of the xanthophyll cycle in the dissipation of excess light. Plant Physiol 84: 218–224

    Google Scholar 

  • Demmig B, Winter K, Kruger A and Czygan F-C (1988) Zeaxanthin and the heat dissipation of excess light energy in Nerium oleander exposed to a combination of high light and water stress. Plant Physiol 87: 17–24

    Google Scholar 

  • Demmig-Adams B (1990) Carotenoids and photoprotection in plants: A role for the xanthophyll zeaxanthin. Biochim Biophys Acta 1020: 1–24

    Google Scholar 

  • Demmig-Adams B and AdamsIII WW (1990) The carotenoid zeaxanthin and ‘high-energy-state quenching’ of chlorophyll fluorescence. Photosynth Res 25: 187–198

    Google Scholar 

  • Demmig-Adams B, Adams WW, Heber U, Neimanis S, Winter K, Kruger A, Czygan FC, Bilger W and Björkman O (1990) Inhibition of zeaxanthin formation and of rapid changes in radiationless energy dissipation by dithiothreitol in spinach leaves and chloroplasts. Plant Physiol 92: 293–301

    Google Scholar 

  • Demmig-Adams B, Winter K, Kruger A and Czygan FC (1989) Zeaxanthin and the induction and relaxation kinetics of the dissipation of excess excitation energy in leaves in 2% O2, 0% CO2. Plant Physiol 90: 887–893

    Google Scholar 

  • Genty B, Briantais J-M and Baker NR (1989) The relationship between quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochim Biophys Acta 990: 87–92

    Google Scholar 

  • Horton P and Hague A (1988) Studies on the induction of chlorophyll fluorescence in isolated barley protoplasts. IV. Resolution of non-photochemical quenching. Biochim Biophys Acta 932: 107–115

    Google Scholar 

  • Horton P, Noctor G and Rees D (1990) Regulation of light harvesting and electron transport in Photosystem II. In: Zelitch I (ed) Perspectives in Biochemical and Genetic Regulation of Photosynthesis, pp 145–158. Alan Liss Inc., New York

    Google Scholar 

  • Horton P, Ruban AV, Rees D, Pascall AA, Noctor G and Young AJ (1991) Control of the light-harvesting function of chloroplast membranes by aggregation of the LHC II chlorophyll-protein complex. FEBS Lett 292: 1–4

    Google Scholar 

  • Krause GH and Behrend U (1983) Characterization of chlorophyll fluorescence quenching in chloroplasts by fluorescence spectroscopy at 77 K. II. ATP-dependent quenching. Biochim Biophys Acta 723: 176–181

    Google Scholar 

  • Krause GH and Laasch H (1987) Energy-dependent chlorophyll fluorescence quenching in chloroplasts correlated with quantum yield of photosynthesis. Z Naturforsch 42: 581–584

    Google Scholar 

  • Krause GH, Laasch H and Weis E (1988) Regulation of thermal dissipation of absorbed light energy in chloroplasts indicated by energy dependent fluorescence quenching. Plant Physiol Biochem 26: 445–452

    Google Scholar 

  • Krause GH, Vernotte C and Briantais J-M (1982) Photoinduced quenching of chlorophyll fluorescence in intact chloroplasts and algae. Resolution into two components. Biochim Biophys Acta 679: 116–124

    Google Scholar 

  • Mills J and Barber J (1975) Energy-dependent cation-induced control of chlorophyll a fluorescence in isolated intact chloroplasts. Archives Biochem Biophys 170: 306–314

    Google Scholar 

  • Neubauer C and Schreiber U (1987) The polyphasic rise of chlorophyll fluorescence upon upset of strong continuous illumination. I. Saturation characteristics and partial control by the Photosystem II acceptor side. Z Naturforsch 42c: 1246–1254

    Google Scholar 

  • Noctor G, Rees D, Young A and Horton P (1991) The relationship between zeaxanthin, energy-dependent quenching of chlorophyll fluorescence, and trans-thylakoid pH gradient in isolated chloroplasts. Biochim Biophys Acta 1057: 320–330

    Google Scholar 

  • Oxborough K and Horton P (1988) A study of the regulation and function of energy-dependent quenching in pea chloroplasts. Biochim Biophys Acta 934: 135–143

    Google Scholar 

  • Quick WP and Horton P (1984) Studies on the induction of chlorophyll fluorescence in barley protoplasts. II. Resolution of fluorescence quenching by redox state and the transthylakoid pH gradient. Proc R Soc Lond B 220: 371–382

    Google Scholar 

  • Rees D, Noctor GD and Horton P (1990) The effect of high-energy-state excitation quenching on maximum and dark level chlorophyll fluorescence yield. Photosynth Res 25: 199–212

    Google Scholar 

  • Rees D, Young A, Noctor G, Britton G and Horton P (1989) Enhancement of the pH-dependent dissipation of excitation energy in spinach chloroplasts by light-activation: Correlation with the synthesis of zeaxanthin. FEBS Lett 256: 85–90

    Google Scholar 

  • Rijgersberg CP, Amesz J, Thielen APGM and Swager JA (1979) Fluorescence emission spectra of chloroplasts and subchloroplast preparations at low temperature. Biochim Biophys Acta 545: 473–482

    Google Scholar 

  • Ruban AV, Rees D, Noctor GD, Young A and Horton P (1991) Long wavelength chlorophyll species are associated with amplification of high-energy-state excitation quenching in higher plants. Biochim Biophys Acta 1059: 355–360

    Google Scholar 

  • Schreiber U and Neubauer C (1989) Correlation between dissipative fluorescence quenching at Photosystem II and 50 μs recombination luminescence. FEBS Lett 258: 339–342

    Google Scholar 

  • Vernotte C, Etienne AL and Briantais J-M (1979) Quenching of the system 2 chlorophyll fluorescence by the plastoquinone pool. Biochim Biophys Acta 545: 519–527

    Google Scholar 

  • Weis E and Berry JA (1987) Quantum efficiency of PS 2 in relation to ‘energy’ dependent quenching of chlorophyll fluorescence. Biochim Biophys Acta 894: 198–208

    Google Scholar 

  • Wraight CA, Kraan GPB and Gerrits NM (1972) The pH dependence of delayed and prompt fluorescence in uncoupled chloroplasts. Biochim Biophys Acta 283: 259–267

    Google Scholar 

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Rees, D., Noctor, G., Ruban, A.V. et al. pH dependent chlorophyll fluorescence quenching in spinach thylakoids from light treated or dark adapted leaves. Photosynth Res 31, 11–19 (1992). https://doi.org/10.1007/BF00049532

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  • DOI: https://doi.org/10.1007/BF00049532

Key words

  • carotenoid
  • chlorophyll fluorescence
  • non-photochemical quenching
  • pH
  • photosynthesis
  • zeaxanthin