Roles of three lumen-surface proteins in the formation of S2 state and O2 evolution in Photosystem II particles from spinach thylakoid membranes

1986 ◽  
Vol 848 (2) ◽  
pp. 201-211 ◽  
Author(s):  
Akiko Imaoka ◽  
Kozo Akabori ◽  
Masayuki Yanagi ◽  
Kaori Izumi ◽  
Yoshinori Toyoshima ◽  
...  
FEBS Letters ◽  
1981 ◽  
Vol 134 (2) ◽  
pp. 231-234 ◽  
Author(s):  
Deborah A. Berthold ◽  
Gerald T. Babcock ◽  
Charles F. Yocum

1985 ◽  
Vol 808 (2) ◽  
pp. 348-351 ◽  
Author(s):  
Jean-Marie Briantais ◽  
Claudie Vernotte ◽  
Mitsue Miyao ◽  
Norio Murata ◽  
Martine Picaud

1981 ◽  
Vol 194 (3) ◽  
pp. 877-887 ◽  
Author(s):  
A C Stewart ◽  
D S Bendall

1. O2-evolving Photosystem-II particles from the thermophilic blue–green alga Phormidium laminosum contained 1 mol of Mn/13–17 mol of chlorophyll a compared with 1 mol of Mn/65–75 mol of chlorophyll a in unfractionated membranes. 2. At least two-thirds of the Mn in the Photosystem-II particles was removed by mild heating and by treatment with Tris or EDTA, with concomitant loss of O2 evolution. However, irreversible inactivation was also caused by washing in buffers without MgCl2, and this inactivation was not accompanied by a corresponding loss of Mn. 3. Bivalent cations (Mg2+ or Ca2+), Cl- or Br- ions and at least 20% (v/v) glycerol were required for maximum stability of O2 evolution. 4. The Photosystem-II particles were enriched in high-potential cytochrome b-559 (1 mol of cytochrome/50–60 mol of chlorophyll a) and in component C-550, and had a photosynthetic-unit size of 40–70 molecules of chlorophyll a. 5. The absorption spectrum at 77 K showed a preponderance of shorter-wavelength forms of chlorophyll a in the Photosystem-II particles, and in the fluorescence emission spectrum at 77 K there were major chlorophyll fluorescence bands at 684 nm and 695 nm, with almost no fluorescence in the far-red region. 6. Analysis of the lipid and protein contents showed that the Photosystem-II particles were not chemically pure (for example, all of the membrane-bound cytochromes and cytochrome c-549 were present), but their high O2-evolution activity and good optical properties make them useful for functional studies on Photosystem-II and O2 evolution.


1991 ◽  
Vol 46 (1-2) ◽  
pp. 87-92 ◽  
Author(s):  
S. C. Sabat ◽  
V. Vijayavergiya ◽  
B. C. Tripathy ◽  
Prasanna Mohanty

Abstract The effect of K-picrate-18-crown-6 (crown) on the photoelectron transport activity of beet spinach thylakoid membranes was investigated. Addition of micromolar concentration of crown to thylakoid preparation inhibited p-benzoquinone, chloride-indophenol, methyl viologen supported Hill activities maximally by 75 per cent in a concentration dependent manner. However, the photosystem I catalyzed reaction remained insensitive to crown suggesting that crown specifically inhibits photosystem II electron transport. Addition of exogenous electron donors like hydroxylamine or diphenylcarbazide failed to restore the crown induced inhibition of photosystem II electron transport and lowering of steady state chlorophyll a fluorescence yield. These observations suggest that crown also inhibits photosystem II catalyzed electron transport after the donation sites of these exogenous donors. Washing of the crown pre-treated thylakoids with isolation buffer, relieved the crown inhibited electron transport activity, indicating that this inhibition is reversible. Furthermore, in hydroxylamine washed thylakoids which are devoid of O2 evolution capacity, the hydroxylamine induced increase in chlorophyll a fluorescence of variable yield was quenched by the addition of crown. These observations suggest that crown affects the oxygen evolution and inhibits at a site close to photosystem II reaction centres.


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