Glycinebetaine Stabilizes Photosystem 1 and Photosystem 2 Electron Transport in Spinach Thylakoid Membranes Against Heat Inactivation

1999 ◽  
Vol 37 (3) ◽  
pp. 423-432 ◽  
Author(s):  
Y.M. Allakhverdieva ◽  
M.D. Mamedov ◽  
N. Ferimazova ◽  
G.C. Papageorgiou ◽  
R.A. Gasanov
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.


1993 ◽  
Vol 48 (3-4) ◽  
pp. 163-167
Author(s):  
Koichi Yoneyama ◽  
Yoshihiro Nakajima ◽  
Masaru Ogasawara ◽  
Hitoshi Kuramochi ◽  
Makoto Konnai ◽  
...  

Abstract Through the studies on structure-activity relationships of 5-acyl-3-(1-aminoalkylidene)-4-hydroxy-2 H-pyran-2,6(3 H)-dione derivatives in photosystem II (PS II) inhibition, overall lipophilicity of the molecule was found to be a major determinant for the activity. In the substituted N -benzyl derivatives, not only the lipophilicity but also the electronic and steric characters of the substituents greatly affected the activity. Their mode of PS II inhibition seemed to be similar to that of DCMU , whereas pyran-enamine derivatives needed to be highly lipophilic to block the electron transport in thylakoid membranes, which in turn diminished the permeability through biomembranes.


2008 ◽  
Vol 1778 (4) ◽  
pp. 997-1003 ◽  
Author(s):  
Sashka B. Krumova ◽  
Cor Dijkema ◽  
Pieter de Waard ◽  
Henk Van As ◽  
Győző Garab ◽  
...  

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