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  • Photosystem II
  • Springer  (7)
  • Elsevier
  • Institute of Physics
  • Oxford University Press
  • 1980-1984  (7)
Collection
Publisher
  • Springer  (7)
  • Elsevier
  • Institute of Physics
  • Oxford University Press
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 138 (1984), S. 299-305 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Oscillatoria ; Anoxygenic photosynthesis ; Sulfide ; Photosystem II ; Photoreduction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Oscillatoria amphigranulata is a fast-growing (3 doublings/day) cyanobacterium isolated from sulfide hot springs in New Zealand. Photosynthesis, as measured by incorporation of [14C]-HCO 3 - , was initially inhibited by 0.3–1.5 mM sulfide at pH 7.9–8.1. However, conversion to sulfide-dependent anoxygenic photosynthesis occurred in about 2 h or less under light intensities of 3–14 klx. Under the stimulation of higher light intensity (8–14 klx) a partial recovery of oxygenic photosynthesis also occurred. It was concluded that oxygenic photosynthesis was responsible for 21–42% of the total incorporation at sulfide concentrations of 1.0–0.3 mM, respectively. This contribution was suppressed at 1.5 mM sulfide and not elicited under lower light intensities (3–7 klx). As judged by the inhibitory effect of 10 μg/ml chloramphenicol protein synthesis was required for attainment of both anoxygenic photosynthesis and photosystem II recovery. Sulfide could not be replaced by thiosulfate, elemental sulfur or dithionite as electron donors in photosynthesis, but elemental sulfur could serve as the sole assimilatory source of sulfur. Oxygenic photosynthesis was inhibited by DCMU [3-(3,4-dichlorophenyl)-1,1-dimethylurea] or DBMIB (2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone), but sulfide relieved the effect of either inhibitor in adapted cells, indicating that electrons derived from sulfide enter the photosynthetic electron transport chain at a point beyond plastoquinone.
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  • 2
    ISSN: 1432-2048
    Keywords: Cyanobacteria ; Fluorescence induction (chlorophyll) ; Microcystis ; Photoinhibition ; Photosynthesis (electron transport) ; Photosystem II
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Sites of photoinhibition and photo-oxidative damage to the photosynthetic electrontransport system of the unicellular cyanobacterium Microcystis aeruginosa were identified by studies of the kinetics of chlorophyll fluorescence induction by whole cells at room temperature and from partial photosynthetic electron-transport reactions in vitro in thylakoid preparations. Chlorophyll fluorescence intensity decreased following photoinhibitory light treatment. This was attributed to decreases both in the activity of photosystem II and in electron flow through the primary electron acceptor, Q. This inhibition was only partially reversed over a 50-min dark recovery period. Partial photosynthetic electron-transport experiments in vitro demonstrated that photosystem I was not affected by the photoinhibitory treatment. Light damage was associated exclusively with the light reactions, of photosystem II, at a site close to the reaction centre, between the site where diphenylcarbazide can donate electrons and the site where silicomolybdate can accept electrons. This damage presumably reduced production of ATP by noncyclic photophosphorylation and production of NADPH by photosystem I, decreasing the availability of these co-factors for reducing CO2 in the ‘dark’ reactions of photosynthesis. The importance of these findings is discussed.
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  • 3
    ISSN: 1432-2048
    Keywords: Chlorophyll fluorescence ; Commelina ; Guard cell ; Oxygen evolution (guard cell) ; Photosystem II ; Protoplast
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Guard-cell protoplasts were isolated by enzymic digestion of the epidermis peeled from the abaxial surface of leaves from Commelina communis L. The protoplasts were separated from mesophyll-cell protoplasts and other contaminants by density-gradient centrifugation, and the purity of the preparations carefully and quantitatively assessed by light microscopy. The preparations of guard-cell protoplasts were then compared with mesophyll-cell protoplasts in terms of the activity of photosystem II as assessed by a) the light-induced evolution of oxygen under both steady-state and flashing light and b) the characteristics of photosystem-II chlorophyll fluorescence. In all experiments, clear photosystem-II activity was found in guard-cell protoplasts, although some subtle distinctions between guard-cell and mesophyll-cell protoplasts were found. The contribution of any contaimination by mesophyll-cell chlorophyll to guard-cell-protoplast signals was estimated to be less than 3% in all cases. The results indicate that photosystem II is present and active in guard cells of Commelina.
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  • 4
    ISSN: 1432-2048
    Keywords: Charge density ; Chlorophyll fluorescence ; Heat sensitivity ; Oxygen evolution ; Photosystem II ; Thylakoid membrane ; Spinacia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The heat-sensitivity of photosynthetic oxygen evolution of thylakoids isolated from spinach increases by increasing the pH above neutral value. The temperature for inactivation (transition temperature) is lowered from about 45° C (pH 6.0–7.4) to 33°C (pH 8.5). Similar results are obtained with intact chloroplasts. At pH 7.0 the transition temperature of washed thylakoids decreases by lowering the salt concentration below 20 mM with monovalent cations (Li+, Na+, K+) and below 3–4 mM with divalent cations (Mg2+, Ca2+, Sr2+). Illumination decreases the heat-sensitivity of oxygen evolution in intact chloroplasts, but even increases the heat-sensitivity in uncoupled chloroplasts. In intact chloroplasts the transition temperature of the heat-induced rise in chlorophyll fluorescence yield (Fo; see Schreiber and Armond 1978) decreases from 44° C to 38° C when the pH of the suspending medium is increased from 6.5 to 8.5. At 20° C, Fo is almost insensitive to pH (6.0–8.5). At 40° C, however, Fo is constant between 6.0 and 7.0, but strongly increases by increasing the pH above neutral value. The results are discussed in terms of a close relation between electrostatic forces at the thylakoid membrane and thermal sensitivity of photosynthetic apparatus. It is suggested that the heat-sensitivity of the photosystem II complex partially depends on the ionization state of fixed groups having alkaline pK. The “packed volume” of thylakoids suspended in a low salt medium increases when the temperature is increased above 30° C (pH 7.0) and above 20° C (pH 8.0), respectively. This result suggests a heat-induced increase in surface charge density of the thylakoid membrane.
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  • 5
    ISSN: 1573-5079
    Keywords: Delayed light Emission ; Hydroxylamine ; Photosynthesis ; Photosystem II ; Sillicomolybdate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Measurements are reported on μs delayed light emission, following a single 10 ns excitation flash, in Alaska pea thylakoids treated with hydroxylamine (NH2OH) or with silicomolybdate. 1. In thylakoids treated with 2 mM NH2OH in the light, or in the dark, the quantum yield of delayed light emission is considerably enhanced. A 10 μs lifetime component of delayed light emission is not significantly changed, whereas a 50–70 μs lifetime component is increased. MnCl2 and diphenylcarbazide are unable to reverse the above effects of NH2OH treatment. Thus Mn2+ and diphenylcarbazide must not donate electrons directly to reaction center II but on the oxygen-evolution side of the NH2OH block. 2. When the closed form of photosystem II reaction centers (P680Q-), where P680 is the reaction center chlorophyll and Q is a ‘stable’ electron acceptor, is generated by preillumination of NH2OH-treated thylakoids with diuron present, the μs delayed light emission is inhibited, but a low level residual delayed light emission remains. Possible origins of this emission are discussed. It is believed that the best explanation for residual DLE is the existence of another acceptor besides Q that partakes in charge separation and rapid dissipative recombination when the reaction center is in the P680Q- state. 3. The quantum yield of delayed light emission from ‘closed’ reaction centers (P680 +Q-) that have all charge stabilization reactions (i.e., flow of electrons to P680 + and out of Q-) blocked by NH2OH treatment and addition of diuron is 1.1×10-3 for components measured in a range from 6 to 400 μs and extrapolated to zero time. 4. The addition of silicomolybdate, which accepts electron from Q-, causes delayed light emission in the μs range to be greatly inhibited.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of bioenergetics and biomembranes 14 (1982), S. 249-264 
    ISSN: 1573-6881
    Keywords: Photosystem II ; photosystem II site-specificity ; chloroplast membranes ; ATPase proton pump ; proton processing ; intramembrane proton interaction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Physics
    Notes: Abstract The chloroplast thylakoid ATPase proton pump-driven H+ accumulation in the dark was compared to the light-dependent proton pump driven by either photosystem II or I, in regard to the effects of the resultant acidity on chemical modification reactions. The assays used to detect the acidity effects were: (a) the incorporation of [3H]-acetic anhydride into membrane protein −NH2 groups, and (b) the effect of a certain level of that chemical modification on inhibition of photosystem II water oxidation activity. Based on labeling data with [3H]-acetic anhydride, 20–30 nmol · (mg chl)−1 of −NH 3 + groups appear to be metastable in the dark in untreated membranes. The term metastable is used because proton leak-inducing treatments in the dark lead to about 20–30 nmol · (mg chl)−1 increase in acetic anhydride labeling, probably due to reaction with the −NH2 form of amine groups. Addition of low levels of uncoupler or a brief thermal treatment caused a loss of protons from the membrane equivalent to the increase in acetic anhydride derivatization. The increase in acetic anhydride derivatization caused inhibition of water oxidation activity. Using thermally sensitized membranes, photosystem II but not photosystem I electron transport (each giving a steady-state proton accumulation of about 50 nmol H+ · (mg chl)−1 restored the lower level of acetic anhydride reactivity as in previous results (Bakeret al., 1981). In dark-maintained, thermally treated membranes, ATPase activity, i.e., the proton pump associated with it, also restored the lower level of acetic anhydride labeling, and again acetic anhydride no longer inhibited water oxidation. Because photosystem I activity did not elicit this type of response to acetic anhydride, there appears to be a pathway for ATPase pumped protons which allows them to reach a restricted domain, perhaps intramembrane, common with the photosystem II water oxidation mechanism and unavailable to protons pumped by photosystem I. The membrane structure(s) which determines this site specificity is not yet understood.
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  • 7
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Fluorescence induction ; Oxygen evolution ; Photosystem II ; DCMU-sensitivity ; Electron transport ; Oscillatoria chalybea
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The filamentous cyanobacterium Oscillatoria chalybea grows phototrophically on a mineral medium in the presence of either nitrate or ammonium ions as nitrogen source at similar growth rates. In the absence of any combined nitrogen source in the medium the cyanobacterium also grows, although at a reduced growth rate. The steady state rate of oxygen evolution by filaments from these three culture conditions is approximately constant if compared on an equal chlorophyll basis. Qualitative differences, however, emerge, if transient phenomena, e.g. the oxygen gush, are investigated. Only nitrate-and nitrogen-free-grown cultures show an oxygen gush, whereas ammonium sulfate-grown cultures do not show this phenomenon. Fluorescence induction in O. chalybea shows a fast monophasic rise, comparable to the fluorescence rise curves of higher plant chloroplasts in the presence of dithionite. The steady state level of fluorescence in ammonium sulfate-grown cells is up to seven times higher than in nitrate-grown cells when compared on an equal chlorophyll basis. In ammonium sulfate-grown cells, DCMU (N,N′-3,4-Dichlorophenyl dimethylurea) causes a further increase in fluorescence level. In nitrate-grown cyanobacteria, however, the effect of DCMU consists of a decrease of the steady state level of fluorescence. In context with earlier research on Anabaena cylindrica, another filamentous cyanobacterium, it appears that the type of the nitrogen source used for growth determines the main location of the DCMU-block in this organism. It thus appears that in O. chalybea the site of DCMU inhibition lies on the oxygen-evolving side of photosystem II, if the organism is grown on nitrate. If grown on ammonium sulfate, no substantial difference of the location of the inhibition site when compared to algae or higher plant chloroplasts is found. Thylakoid preparations of O. chalybea perform the usual Hill reactions with ferricyanide, p-benzoquinone or silicomolybdate as electron acceptors. In each case it is seen that with thylakoids of nitrate-grown cells the steady-state level of fluorescence is lowered by DCMU in the presence of these acceptors, which should be the case, if DCMU inhibits electron transfer on the donor side of photosystem II. According to the literature silicomolybdate accepts electrons mainly before the DCMU-block in higher plant chloroplasts. Hence, in higher plants this reaction is mainly DCMU-insensitive. In thylakoids of O. chalybea, however, the Hill reaction with silicomolybdate is DCMU-sensitive which provides further evidence that the DCMU-block is on the oxygen-evolving side of photosystem II in O. chalybea provided the cells have been grown on nitrate.
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