1987
DOI: 10.1016/0014-5793(87)80322-8
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Direct observation of the immediate electron donor to chlorophyll‐a+II(P‐680+) in oxygen‐evolving photosystem II complexes Resolution of nanosecond kinetics in the UV

Abstract: Flash-induced absorption changes in the UV have been monitored with nanosecond time resolution in oxygen-evolving photosystem II complexes from Synechococcus sp. At 260 nm, the oxidation of the immediate donor to Chl-a: (P-680+) in the l&500 ns range could be observed directly. The difference extinction coefficient for its oxidation is estimated to be 6000-8000 M-l .cm-' at 260 nm. The observed kinetics for the oxidation of the donor is identical with the reduction kinetics of Chl-a: as monitored at 824 nm. At… Show more

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Cited by 32 publications
(9 citation statements)
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“…Leaving out heterogeneity in the manganese cluster, the scheme is linear with only Yz carrying electrons from manganese to P^o• The dependence of the electron-transfer rates on S state may be due to electrostatic effects resulting from varying charge distributions in the OEC in the different S states. Recent time-resolved optical measurements at 260 and 824 nm also support the idea that Yz is the only donor between P680 and the OEC (Gerken et al, 1987).…”
Section: Discussionmentioning
confidence: 79%
“…Leaving out heterogeneity in the manganese cluster, the scheme is linear with only Yz carrying electrons from manganese to P^o• The dependence of the electron-transfer rates on S state may be due to electrostatic effects resulting from varying charge distributions in the OEC in the different S states. Recent time-resolved optical measurements at 260 and 824 nm also support the idea that Yz is the only donor between P680 and the OEC (Gerken et al, 1987).…”
Section: Discussionmentioning
confidence: 79%
“…The fast and slow kinetic phases of menasemiquinone oxidation were measured optically on the nanosecond time scale by monitoring the flash‐induced transient absorption change at 380 nm using a time‐resolved spectrophotometer similar to that described in Gerken et al . (22). The excitation beam was provided by a frequency‐doubled (λ = 532 nm), Q‐switched Nd:YAG laser (DCR‐11; Spectra Physics, Mountain View, CA) operated in the short pulse mode (∼3 ns).…”
mentioning
confidence: 99%
“…Spectroscopic Measurements. Flash-induced absorbance measurements with a time resolution of 5 ns were performed with the setup described by Gerken et al (1987), using repetitive excitation (1.7 Hz) by 532-nm laser flashes of 3-ns duration, approximately 2 mJ/cm2. The bandwidth (full width at half-maximum) of the measuring beam was usually between 7 and 10 nm, except for measurements at 450 and 488 nm where it was only 3 nm.…”
mentioning
confidence: 99%