Light-harvesting chlorophyll a-b complex requirement for regulation of Photosystem II photochemistry by non-photochemical quenching
- 68 Downloads
- 22 Citations
Abstract
Recently, it has been suggested (Horton et al. 1992) that aggregation of the light-harvesting a-b complex (LHC II) in vitro reflects the processes which occur in vivo during fluorescence induction and related to the major non-photochemical quenching (qE). Therefore the requirement of this chlorophyll a-b containing protein complex to produce qN was investigated by comparison of two barley mutants either lacking (chlorina f2) or depressed (chlorina104) in LHC II to the wild-type and pea leaves submitted to intermittent light (IL) and during their greening in continuous light.
It was observed that qN was photoinduced in the absence of LHC II, i.e. in IL grown pea leaves and the barley mutants. Nevertheless, in these leaves qN had no (IL, peas) or little (barley mutants) inhibitory effect on the photochemical efficiency of QA reduction measured by flash dosage response curves of the chlorophyll fluorescence yield increase induced by a single turn-over flash
During greening in continuous light of IL pea leaves, an inhibitory effect on QA photoreduction associated to qN developed as Photosystem II antenna size increased with LHC II synthesis. Utilizing data from the literature on connectivity between PS II units versus antenna size, the following hypothesis is put forward to explain the results summarized above. qN can occur in the core antenna or Reaction Center of a fraction of PS II units and these units will not exhibit variable fluorescence. Other PS II units are quenched indirectly through PS II-PS II exciton transfer which develops as the proportion of connected PS II units increases through LHC II synthesis.
Key words
chlorophyll fluorescence flash-induced QA photoreduction greening light-harvesting chlorophyll a-b complex non-photochemical quenching Photosystem II photochemical efficiencyAbbreviations
- F
chlorophyll fluorescence levels, subscripts o and m are minimal and maximal levels of darkadapted leaves
- o′, m′ and s
minimal, maximal and steady state levels in the presence of actinic light
- Fv and Fv′
(Fm-Fo) and (Fm′-Fo′) respectively
- ΔF
(Fm′-Fs)
- δF
single turn-over flash-induced fluorescence yield increase
- δFmax
single turn-over saturating flash-induced fluorescence yield increase
- IL
intermittent light
- LHC II
light-harvesting chl a-b complex associated with PS II
- PFD
photon flux density
- PS II
Photosystem II
- QA
primary quinonic electron acceptor of PS II
- qP
photochemical quenching
- qN
non-photochemical quenching
- σ
relative efficiency of PS II photoreduction of QA
- σd
σ of dark-adapted leaves
Preview
Unable to display preview. Download preview PDF.
References
- Argyroudi-Akoyunoglou JH and Akoyunoglou G (1970) Photoinduced changes in the chlorophyll a to chlorophyll b ratio in young bean plants. Plant Physiol 46: 247–249Google Scholar
- Armond PA, Arntzen CJ, Briantais JM and Vernotte C (1976) Differentiation of chloroplast lamellae, ligh-harvesting efficiency and grana development. Arch Biochem Biophys 175: 54–63PubMedGoogle Scholar
- Arntzen CJ, Armond PA, Briantais JM, Burke JJ and Novitzky WP (1976) Dynamic interactions among structural components of the chloroplast membrane; in chlorophyll-proteins, reaction centers and photosynthetic membranes. Brookhaven Symposia in Biology no, 28: 316–337Google Scholar
- Briantais JM, Vernotte C, Picaud M and Krause GH (1979) A quantitative study of the slow decline of chlorophyll a fluorescence in isolated chloroplats. biochim Biophys Acta 548: 128–138PubMedGoogle Scholar
- Brugnoli E and Bjorkman O (1992) Chloroplast movements in leaves: Influence on chlorophyl fluorescence and measurements of light-induced absorption changes related to ΔpH and zeaxanthin formation. Photosynth Res 32: 23–35Google Scholar
- Crofts J and Horton P (1991) Dissipation of excitation energy by Photosystem II particles at low pH. Biochim Biophys Acta 1058: 187–193Google Scholar
- Falkowski PG, Wyman K, Ley AC and Mauzerall DC (1986) Relationship of steady-state photosynthesis to fluorescence in eukariotic algae. Biochim Biophys Acta 849: 183–192Google Scholar
- Genty B, Briantais JM and Baker NR (1989) The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochim Biophys Acta 990: 87–92Google Scholar
- Genty B, Wonders J and Baker NR (1990a) Non-photochemical quenching of Fo in leaves is emission wavelength dependent: Consequences for quenching analysis and its interpretation. Photosynth Res 26: 133–139Google Scholar
- Genty B, Harbinson J, Briantais JM and Baker NR (1990b) The relationship between non-photochemical quenching of chlorophyll fluorescence and the rate of Photosystem 2 photochemistry in leaves. Photosynth Res 25: 219–257Google Scholar
- Genty B, Harbinson J, Briantais JM and Baker NR (1990c) The relationship between the relative quantum efficiencies of photosystems in leaves. Efficiency of PS II in relation to nonphotochemical fluorescence quenching. In: Baltscheffsky M (ed) Current Research in Photosynthesis, Vol IV, pp 365–368 Kluwer Academic Publishers, DordrechtGoogle Scholar
- Genty B, Goulas Y, Dimon B, Peltier G, Briantais JM and Moya I (1992) Modulation of efficiency of primary conyersion in leaves, mechanisms in volved at PS II. In: Murata N (ed) Research in Photosynthesis, Vol IV, pp 603–610 Kluwer Academic Publishers, Dordrecht.Google Scholar
- Hodges M, Cornic G and Briantais JM (1989) Chlorophyll fluorescence from Spinach leaves. Resolution of non-photechemical quenching. Biochim Biophys Acta 974: 289–293Google Scholar
- Horton P and Hague A (1988) Studies on the induction of chlorophyll fluorescence in isolated barley protoplasts. IV. Resolution of nonphotochemical quenching. Biochim Biophys Acta 932: 107–115Google Scholar
- Horton P and Ruban AV (1992). Regulation of Photosystem II. Photosynth Res 34: 375–385Google Scholar
- Horton B Ruben AV, Sees D, Pascal AA, Noctor GD and Young AJ (1992) Control of the light-harvesting function of chloroplast membranes by aggregation of the LCHII chlorophyll protein complex. FEBS Lett 292: 1–4CrossRefGoogle Scholar
- Knoetzel J and Simpson D (1991) Expression and organization of antenna proteins in the light and temperature-sensitive barley mutant Chlorina-104 Planta 185: 111–123CrossRefGoogle Scholar
- Krieger A and Weis E (1990) pH-dependent quenching of chlorophyll fluorescence in isolated PS II particles: Dependence on the redox-potential. In: Baltscheffsky M (ed) Current Ressearch in Photosynthesis. Vol. VI, pp 563–566, Kluwer Academic Publishers, DordreehtGoogle Scholar
- Lokstein H, Hërtel H and Hoffmann-Renger G (1993) comparison of chlorophyli fluorescence quenching in leaves of wild-type with a chlorophyll b less mutant of barley (Hordeum vulgare L.). J Photochem Photobiol B: Biol 19: 217–225CrossRefGoogle Scholar
- Mackinney G (1941) Absorption of light by chlorophyll solutions. J Biol Chem 140: 315–322Google Scholar
- Mauzerall DC (1978) Multiple excitation and the yield of chlorophyll a fluorescence in photosynthetic system. Photochem Photobiol 28: 991–998Google Scholar
- Melis A and Akoyunoglou G (1977) Development of the two hetcrogeneous Photosystem II units in etiolated bean leaves. Plant Physiol 59: 1156–1160Google Scholar
- Peter D and Thornber JP (1991) Biochemical composition and organization of higher plant Photosystem II light-harvesting pigment-proteins. J Biol Chem 266: 16745–16754PubMedGoogle Scholar
- Quick WP and Stitt M (1989) An examination of factors contributing to non-photochemical quenching of chlorophyll fluorescence in barley leaves. Biochim Biophys Acta 977: 287–296Google 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: 199–211Google Scholar
- Rees D, Noctor GD, Ruban AV, Crofts J, Young A and Horton P (1992) pH dependent chlorophyll fluorescence quenching in spinach thylakoids from light-treated or dark-adapted leaves. Photosynth Res 31: 11–19Google Scholar
- Ruban AV and Horten P (1992) Mechanism of ΔpH dependent dissipation of absorbed exoltation energy by photosynthetie membranes. I spectroscople analysis of isolated light-harvesting complexes. Biochim Biophys Acta 1102: 30–38Google Scholar
- Schatz GH, Brock H and Holzwarth (1987) Pleosecond kineties of fluorescence and absorbance changes in Photosystem II particles excited at low photon density. Proc Natl Acad Sci USA 84: 8414–8418Google Scholar
- Schreiber U (1986) Detection of rapid induction kinetics with a new type of high-frequency modulated chlorophyll fluorimeter. Photosynth Res 9: 261–272Google Scholar
- Schreiber U and Neubauer C (1987) The polyphasic rise of chlorophyll fluorescence upon onset of strong continuous illumination: Partial control by the Photosystem II donor side and possible ways of interpretation. Z Naturforsch 42C: 1255–1264Google Scholar
- Walters RG and Horton P (1991) Resolution of components of non-photochemical chlorophyll fluorescence quenching in barley leaves. Photosynth Res 27: 121–133Google Scholar
- Weis E and Berry JA (1987) Quantum efficiency of Photosystem 2 in relation to energy dependent quenching of chlorophyll fluorescence. Biochim Biophys Acta 894: 189–208Google Scholar