Reversible Dissociation of OEC Proteins from the Lumenal Side of the Thylakoid Membranes During Photoinhibition and Recovery

Author(s):  
Y. Domovich ◽  
T. S. Mor ◽  
R. Oelmuller ◽  
R. G. Herrmann ◽  
I. Ohad
2011 ◽  
Vol 62 (7) ◽  
pp. 2393-2402 ◽  
Author(s):  
B. Daum ◽  
W. Kuhlbrandt

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.


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