Literature DB >> 177047

A flash photolysis ESR study of photosystem II signal IIvf, the physiological donor to P-680+.

J T Warden, R E Blankenship, K Sauer.   

Abstract

In flash-illuminated, oxygen-evolving spinach chloroplasts and green algae, a free radical transient has been observed with spectral parameters similar to those of Signal II (g approximately 2.0045, deltaHpp approximately 19G). However, in contrast with ESR Signal II, the transient radical does not readily saturate even at microwave power levels of 200 mW. This species is formed most efficiently with "red" illumination (lambda less than 680 nm) and occurs stoichiometrically in a 1:1 ratio with P-700+. The Photosystem II transient is formed in less than 100 mus and decays via first-order kinetics with a halftime of 400-900 mus. Additionally, the t1/2 for radical decay is temperature independent between 20 and 4 degrees C; however, below 4 degrees C the transient signal exhibits Arrhenius behavior with an activation energy of approx. 10 kcal-mol-1. Inhibition of electron transport through Photosystem II by o-phenanthroline, 3-(3,4-dichlorophenyl)-1,1-dimethylurea or reduced 2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone suppresses the formation of the light-induced transient. At low concentrations (0.2 mM), 2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone partially inhibits the free radical formation, however, the decay kinetics are unaltered. High concentrations of 2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone (1-5 mM) restore both the transient signal and electron flow through Photosystem II. These findings suggest that this "quinoidal" type ESR transient functions as the physiological donor to the oxidized reaction center chlorophyll, P-680+.

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Year:  1976        PMID: 177047     DOI: 10.1016/0005-2728(76)90201-2

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  10 in total

1.  Apparatus and mechanism of photosynthetic oxygen evolution: a personal perspective.

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2.  Defining the far-red limit of photosystem I: the primary charge separation is functional to 840 nm.

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3.  Electron transfer in photosystem II.

Authors:  H J Van Gorkom
Journal:  Photosynth Res       Date:  1985-01       Impact factor: 3.573

4.  The protein environment surrounding tyrosyl radicals D. and Z. in photosystem II: a difference Fourier-transform infrared spectroscopic study.

Authors:  S Kim; B A Barry
Journal:  Biophys J       Date:  1998-05       Impact factor: 4.033

5.  Stoichiometry, inhibitor sensitivity, and organization of manganese associated with photosynthetic oxygen evolution.

Authors:  C F Yocum; C T Yerkes; R E Blankenship; R R Sharp; G T Babcock
Journal:  Proc Natl Acad Sci U S A       Date:  1981-12       Impact factor: 11.205

6.  Changes in [C]Atrazine Binding Associated with the Oxidation-Reduction State of the Secondary Quinone Acceptor of Photosystem II.

Authors:  P Jursinic; A Stemler
Journal:  Plant Physiol       Date:  1983-11       Impact factor: 8.340

7.  Studies on the reconstitution of o(2)-evolution of chloroplasts.

Authors:  R T Sayre; G M Cheniae
Journal:  Plant Physiol       Date:  1982-05       Impact factor: 8.340

8.  Modification of oxygen evolving center by Tris-washing.

Authors:  T Yamashita
Journal:  Photosynth Res       Date:  1986-01       Impact factor: 3.573

9.  Endor characterization and D2O exchange in the [Formula: see text] radical in photosystem II.

Authors:  T K Chandrashekar; P J O'malley; I Rodriguez; G T Babcock
Journal:  Photosynth Res       Date:  1986-01       Impact factor: 3.573

10.  Structure of donor side components in photosystem II predicted by computer modelling.

Authors:  B Svensson; I Vass; E Cedergren; S Styring
Journal:  EMBO J       Date:  1990-07       Impact factor: 11.598

  10 in total

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