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  • Chlorophyll fluorescence  (2)
  • sulfide-quinone reductase (SQR)  (2)
  • 1
    ISSN: 1432-2048
    Keywords: Chlorophyll fluorescence ; Light absorbance (830 nm) ; P700 ; Photosynthesis ; Quantum yield
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract An improved method is introduced for the determination of the quantum yield of photosystem I. The new method employs saturating light pulses with steep rise characteristics to distinguish, in a given physiological state, centers with an open acceptor side from centers with a reduced acceptor side. The latter do not contribute to PSI quantum yield (ΦI). Oxidation of P700 is measured by a rapid modulation technique using the absorbance change around 830 nm. The quantum yield ΦI is calculated from the amplitude of the rapid phase of absorbance change (ΔA; 830 nm) upon application of a saturation pulse in a given state, divided by the maximal ΔA (830 nm) which is induced by a saturation pulse with far-red background illumination. Using this technique, ΦI can be determined even under conditions of acceptor-side limitation, as for example in the course of a dark-light induction period or after elimination of CO2 from the gas stream. Thus determined ΦI values display a close-to-linear relationship with those for the quantum yield of PSII (ΦII) calculated from chlorophyll fluorescence parameters. It is concluded that the proposed method may provide new information on the activity of the PSI acceptor side and thus help to separate the effects of acceptorside limitation from those of cyclic PSI, whenever a non-linear relationship between ΦII and the P700-reduction level is observed.
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  • 2
    ISSN: 1432-2048
    Keywords: Chlorophyll fluorescence ; Light absorbance (830 nm) ; P700 ; Photosynthesis ; Quantum yield
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract An improved method is introduced for the determination of the quantum yield of photosystem I. The new method employs saturating light pulses with steep rise characteristics to distinguish, in a given physiological state, centers with an open acceptor side from centers with a reduced acceptor side. The latter do not contribute to PSI quantum yield (ΦI). Oxidation of P700 is measured by a rapid modulation technique using the absorbance change around 830 nm. The quantum yield ΦI is calculated from the amplitude of the rapid phase of absorbance change (ΔA; 830 nm) upon application of a saturation pulse in a given state, divided by the maximal ΔA (830 nm) which is induced by a saturation pulse with far-red background illumination. Using this technique, ΦI can be determined even under conditions of acceptor-side limitation, as for example in the course of a dark-light induction period or after elimination of CO2 from the gas stream. Thus determined ΦI values display a close-to-linear relationship with those for the quantum yield of PSII (ΦII) calculated from chlorophyll fluorescence parameters. It is concluded that the proposed method may provide new information on the activity of the PSI acceptor side and thus help to separate the effects of acceptorside limitation from those of cyclic PSI, whenever a non-linear relationship between ΦII and the P700-reduction level is observed.
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  • 3
    ISSN: 1573-5079
    Keywords: sulfide-quinone reductase (SQR) ; Oselllatoria limnetiea ; Chlorobium limicola ; electron transport ; LED array spectrophotometer ; anoxygenic photosynthesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The reduction by sulfide of exogenous ubiquinone is compared to the reduction of cytochromes in chromatophores of Rhodobacter capsulatus. From titrations with sulfide values for Vmax of 300 and 10 μmoles reduced/mg bacteriochlorophyll a·h, and for Km of 5 and 3 μM were estimated, for decyl-ubiquinone-and cytochrome c-reduction, respectively. Both reactions are sensitive to KCN, as has been found for sulfide-quinone reductase (SQR) in Oscillatoria limnetica, which is a flavoprotein. Effects of inhibitors interfering with quinone binding sites suggest that at least part of the electron transport from sulfide in R. capsulatus employs the cytochrome bc 1-complex via the ubiquinone pool.
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  • 4
    ISSN: 1573-5079
    Keywords: sulfide-quinone reductase (SQR) ; electron transport ; Chlorobium ; oxidant-induced reduction of cytochrome b ; cytochrome bc-complex ; menaquinone ; antimycin ; stigmatellin ; NQNO ; anoxygenic photosynthesis ; LED array spectrophotometer
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Reduction of cytochromes in chlorosome-free membranes of Chlorobia was studied anaerobically, with an LED array spectrophotometer. For Chlorobium tepidum these membranes contained 0.2 moles cytochrome per mole of bacteriochlorophyll a. The observed change upon complete reduction of oxidized membranes with dithionite could be satisfactorily fitted with three cytochrome components having absorption peaks at 553 (cyt c), 558 and 563 nm (cyt b), in relative amounts of 5:1:2. About 20% of total cytochrome 553 were reducible by ascorbate. Menaquinol reduced all of the 553-component, and this reduction was sensitive to stigmatellin, NQNO and antimycin A. The reduction was insensitive to KCN. However, it was transient at low concentrations of menaquinol in the absence of KCN, but permanent in its presence, demonstrating that electron transport into an oxidation pool was blocked. The 563-component was only slightly reduced by menaquinol unless NQNO or antimycin were present. The stimulation of cytochrome 563-reduction by these inhibitors was more pronounced in the presence of ferricyanide. This phenomenon reflects ‘oxidant-induced reduction’ of cytochrome b and demonstrates that a Q-cycle is operative in Chlorobia. Also, sulfide fully reduced cytochrome 553, but more slowly than menaquinol. KCN inhibited in this case, as did stigmatellin, NQNO and antimycin A. NQNO was a better inhibitor than antimycin A. Cytochrome 563 again was hardly reduced unless antimycin A was added. The effect was more difficult to observe with NQNO. This supports the conclusion that sulfide oxidation proceeds via the quinone pool and the cytochrome bc-complex in green sulfur bacteria.
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