Mechanisms for controlling balance between light input and utilisation in the salt tolerant alga Dunaliella C9AA
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Abstract
The yield of photosynthetic O2 evolution was measured in cultures of Dunaliella C9AA over a range of light intensities, and a range of low temperatures at constant light intensity. Changes in the rate of charge separation at Photosystem I (PS I) and Photosystem II (PS II) were estimated by the parameters ΦPS I and ΦPS II . ΦPS I is calculated on the basis of the proportion of centres in the correct redox state for charge separation to occur, as measured spectrophotometrically. ΦPS II is calculated using chlorophyll fluorescence to estimate the proportion of centres in the correct redox state, and also to estimate limitations in excitation delivery to reaction centres. With both increasing light intensity and decreasing temperature it was found that O2 evolution decreased more than predicted by either ΦPS I or ΦPS II. The results are interpreted as evidence of non-assimilatory electron flow; either linear whole chain, or cyclic around each photosystem.
Key words
chlorophyll fluorescence Dunaliella photosynthesis quantum efficiencyAbbreviations
- F0
dark level of chlorophyll fluorescence yield (PS II centres ‘open’)
- Fm
maximum level of chlorophyll fluorescence yield (PS II centres ‘closed’)
- Fv
variable fluorescence (Fm-F0)
- PS I
Photosystem I
- PS II
Photosystem II
- P700
reaction centre chlorophyll(s) of PS I
- qN
coefficient of non-photochemical quenching of chlorophyll fluorescence
- qP
coefficient of photochemical quenching of fluorescence yield
- qE
high-energy-state quenching coefficient
- ΦPS I
yield of PS I
- ΦPS II
yield of PS II
- ΦS
yield of photosynthetic O2 evolution
- ΦP
intrinsic yield of ‘open’ PS II centres
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References
- AsadaK and BadgerMR (1984) Photoreduction of 18O2 and H2 18O2 with a concomitant evolution of 16O2 in intact spinach chloroplasts. Evidence for scavenging of hydrogen peroxide by peroxidase. Plant Cell Physiol 25: 1169–1179Google Scholar
- AsadaK and TakahashiM (1987) Production and scavenging of active oxygen in photosynthesis. In: KyleDJ, OsmondCB and ArntzenCJ (eds) Photoinhibition, pp 227–287. Elsevier, AmsterdamGoogle Scholar
- AsadaK, NeubauerC, HeberU and SchreiberU (1990) Methyl viologen-dependent cyclic electron transport in spinach chloroplasts in the absence of oxygen. Plant Cell Physiol 31: 557–564Google Scholar
- Ben-HayyimG (1974) Light-induced absorbance changes of the high-potential cytochrome b 559 in chloroplasts. Eur J Biochem 41: 191–196Google Scholar
- BilgerW and SchreiberU (1986) Energy-dependent quenching of dark level chlorophyll fluorescence in intact leaves. Photosynth Res 10: 303–308Google Scholar
- BriantaisJM, VernotteC, PicaudM and KrauseGH (1979) A quantitative study of the slow decline of chlorophyll a fluorescence in isolated chloroplasts. Biochim Biophys Acta 548: 128–138Google Scholar
- BriantaisJ-M, VernotteC, PicaudM and KrauseGH (1980) Chlorophyll fluorescence as a probe for the determination of the photo-induced proton gradient in isolated chloroplasts. Biochim Biophys Acta 591: 198–202Google Scholar
- CramerWA and BohmeH (1972) High-potential cytochrome b 559 as a secondary quencher of chloroplast fluorescence in the presence of 3-(3,4-dichlorophenyl)-1,1-dimethylurea. Biochim Biophys Acta 256: 358–369Google Scholar
- Demmig-AdamsB (1990) Carotenoids and photoprotection in plants: A role for the xanthophyll zeaxanthin. Biochim Biophys Acta 1020: 1–24Google Scholar
- GentyB, BriantaisJ-M and BakerNR (1989) The relationship between quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochim Biophys Acta 990: 87–92Google Scholar
- GentyB, HarbinsonJ, BriantaisJ-M and BakerNR (1990) The relationship between the relative quantum efficiencies of photosystems in leaves. Efficiency of PS II in relation to non-photochemical quenching. In: BaltscheffskyM (ed) Current Research on Photosynthesis, Vol IV, pp 365–368. Kluwer Academic Publishers, Dordrecht, Boston, LondonGoogle Scholar
- GinzburgM and GinzburgBZ (1981) Interrelationships of light, temperature, sodium chloride and carbon source in growth of halotolerant and halophilic strains of Dunaliella. British Phycol J 16: 313–324Google Scholar
- HajibagheriMA, GilmourDJ, CollinsJC and FlowersTJ (1986) X-ray microanalysis and ultrastructural studies of cell compartments of Dunaliella parva. J Exp Bot 37: 1725–1732Google Scholar
- HarbinsonJ and WoodwardFI (1987) The use of light-induced absorbance changes at 820 nm to monitor the oxidation state of P-700 in leaves. Plant Cell Environ 10: 131–140Google Scholar
- HarbinsonJ, GentyB and BakerNR (1989) Relationship between the quantum efficiencies of Photosystems I and II in pea leaves. Plant Physiol 90: 1029–1034Google Scholar
- HarbinsonJ, GentyB and BakerNR (1990) The relationship between CO2 assimilation and electron transport in leaves. Photosynth Res 25: 213–224Google Scholar
- HeberU, KirkMR and BoardmanNK (1979) Photoreactions of cytochrome b 559 and cyclic electron flow in Photosystem II of intact chloroplasts. Biochim Biophys Acta 546: 292–306Google Scholar
- HortonP and HagueA (1988) Studies on the induction of chlorophyll fluorescence in isolated barley protoplasts. IV. Resolution of non-photochemical quenching. Biochim Biophys Acta 932: 107–115Google Scholar
- KrauseGH, VernotteC and BriantaisJ-M (1982) Photo-induced quenching of chlorophyll fluorescence in intact chloroplasts and algae. Resolution into two components. Biochim Biophys Acta 679: 116–124Google Scholar
- LabateCA, AdcockMD and leegoodRC (1991) Effects of temperature on the regulation of photosynthetic carbon assimilation in leaves of maize and barley. Planta 181: 547–554Google Scholar
- LeeCB, ReesD and HortonP (1990) Non-photochemical quenching of chlorophyll fluorescence in the green alga Dunaliella. Photosynth Res 24: 167–173Google Scholar
- MehlerAH (1951) Studies on the reaction of illuminated chloroplasts. II. Stimulation and inhibition of the reaction with molecular oxygen. Arch Biochem Biophys 34: 339–351Google Scholar
- OsmondCB (1981) Photorespiration and photoinhibition. Some implications for the energetics of photosynthesis. Biochim Biophys Acta 639: 77–98Google Scholar
- OxboroughK and HortonP (1988) A study of the regulation and function of energy-dependent quenching in pea chloroplasts. Biochim Biophys Acta 934: 135–143Google Scholar
- PetersFALJ, Van SpanningR and KraayenhofR (1983) Studies on well coupled Photosystem I-enriched subchloroplast vesicles. Optimization of ferredoxin-mediated cyclic photophosphorylation and electric potential generation. Biochim Biophys Acta 724: 159–165Google Scholar
- PetersonRB, SivakMN and WalkerDA (1988) Relationship between steady-state fluorescence yield and photosynthetic efficiency in spinach leaf tissue. Plant Physiol 88: 158–163Google Scholar
- QuickWP and HortonP (1984) Studies on the induction of chlorophyll fluorescence in barley protoplasts. I. Factors affecting the observation of oscillations in the yield of chlorophyll fluorescence and the rate of oxygen evolution. Proc R Soc Lond B 220: 361–370Google Scholar
- QuickWP and StittM (1989) An examination of factors contributing to non-photochemical quenching of fluorescence in barley leaves. Biochim Biophys Acta 977: 287–296Google Scholar
- RadmerR and KokB (1976) Photoreduction of O2 primes and replaces CO2 assimilation. Plant Physiol 58: 336–340Google Scholar
- Radmer R and Ollinger O (1981) Fluorescence and gas exchange in Scenedesmus. Proc 5th Int Congr Photosynth 667–675Google Scholar
- RadmerR, KokB and OllingerO (1978) Kinetics and apparent Km of oxygen cycle under conditions of limiting carbon dioxide fixation. Plant Physiol 61: 915–917Google Scholar
- ReesD and HortonP (1990) The mechanisms of changes in Photosystem II efficiency in spinach thylakoids. Biochim Biophys Acta 1016: 219–227Google Scholar
- ReesD, NoctorGD and HortonP (1990) The effect of high-energy-state excitation quenching on maximum and dark level chlorophyll fluorescence yield. Photosynth Res 25: 199–211Google Scholar
- SchreiberU and NeubauerC (1987) The polyphasic rise of chlorophyll fluorescence upon onset of strong continuous illumination: II. Partial control by the Photosystem II donor side and possible ways of interpretation. Z Naturforsch 42c: 1255–1264Google Scholar
- SchreiberU and NeubauerC (1990) O2-dependent electron flow, membrane energization and the mechanism of non-photochemical quenching of chlorophyll fluorescence. Photosynth Res 25: 279–293Google Scholar
- SchreiberU and RienitsKG (1987) ATP-induced photochemical quenching of variable chlorophyll fluorescence. FEBS Lett 211: 99–104Google Scholar
- SchrieberU, KlughammerC and NeubauerC (1988) Measuring P700 absorbance changes around 830 nm with a new type of pulse modulation system. Z Naturforsch 43c: 686–698Google Scholar
- SeatonGGR and WalkerDA (1990) Chlorophyll fluorescence as a measure of photosynthetic carbon assimilation. Proc Roy Soc B 242: 29–35Google Scholar
- SharkeyTD, BerryJA and SageRF (1988) Regulation of photosynthetic electron-transport in Phaseolus vulgaris L. as determined by room-temperature chlorophyll a fluorescence. Planta 176: 415–424Google Scholar
- SlovacekRE, CrowtherD and HindG (1979) Cytochrome function in the cyclic electron transport pathway of chloroplasts. Biochim Biophys Acta 547: 138–148Google Scholar
- WaltersRG and HortonP (1991) Resolution of components of non-photochemical chlorophyll fluorescence quenching in barley leaves. Photosynth Res 27: 121–134Google Scholar
- WeisE and BerryJA (1987) Quantum efficiency if PS II in relation to ‘energy’ dependent quenching of chlorophyll fluorescence. Biochim Biophys Acta 894: 198–208Google Scholar
- WeisE and LecthenbergD (1989) Fluorescence analysis during steady state photosynthesis. Phil Trans R Soc Lond B 323: 253–268Google Scholar
- WeisE, BallJT and BerryJ (1987) Photosynthetic control of electron transport in leaves of Phaseolus vulgaris: evidence for regulation of PS II by the proton gradient. Proceedings VIIth International Congress on Photosynthesis, BigginsJ (ed) Vol 2, pp 553–556. Martinus Nijhoff, DordrechtGoogle Scholar