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EPR detection of a cryogenically photogenerated intermediate in photosynthetic oxygen evolution
Authors:John L. Casey  Kenneth Sauer
Affiliation:Department of Chemistry and Laboratory of Chemical Biodynamics, Lawrence Berkeley Laboratory University of California Berkeley, CA. 94720 U.S.A.
Abstract:In Photosystem II preparations at low temperature we were able to generate and trap an intermediate state between the S1 and S2 states of the Kok scheme for photosynthetic oxygen evolution. Illumination of dark-adapted, oxygen-evolving Photosystem II preparations at 140 K produces a 320-G-wide EPR signal centered near g = 4.1 when observed at 10 K. This signal is superimposed on a 5-fold larger and somewhat narrower background signal; hence, it is best observed in difference spectra. Warming of illuminated samples to 190 K in the dark results in the disappearance of the light-induced g = 4.1 feature and the appearance of the multiline EPR signal associated with the S2 state. Low-temperature illumination of samples prepared in the S2 state does not produce the g = 4.1 signal. Inhibition of oxygen evolution by incubation of PS II preparations in 0.8 M NaCl buffer or by the addition of 400 μM NH2OH prevents the formation of the g = 4.1 signal. Samples in which oxygen evolution is inhibited by replacement of Cl? with F? exhibit the g = 4.1 signal when illuminated at 140 K, but subsequent warming to 190 K neither depletes the amplitude of this signal nor produces the multiline signal. The broad signal at g = 4.1 is typical for a S = 52 spin system in a rhombic environment, suggesting the involvement of non-heme Fe in photosynthetic oxygen evolution.
Keywords:Photosystem II  Oxygen evolution  EPR  (Spinach chloroplast)  PS  Photosystem  Chl  chlorophyll  Hepes  4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid  Mes  2-(N-morpholino)ethanesulfonic acid
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