Lipids Affect the Charge Stabilization in Wild Type and Mutant Reaction Centers of Photosynthetic Bacteria Rhodobacter Sphaeroides

Author(s):  
Sz. Gedey ◽  
Á. Kecskés ◽  
E. Fodor ◽  
T. Farkas ◽  
L. Nagy
1999 ◽  
Vol 26 (5) ◽  
pp. 465 ◽  
Author(s):  
László Nagy ◽  
Elfrida Fodor ◽  
Júlia Tandori ◽  
László Rinyu ◽  
Tibor Farkas

The effect of lipids on stabilization of electrons on the secondary quinone was studied in reaction centers (RC) of herbicide-sensitive and -resistant (L229Ile → Met) Rhodobacter sphaeroides R-26. The lipid concentration and the lipid/protein ratio of the intracytoplasmic membranes (ICM) were larger in the mutant RCs than in the wild-type. The free energy changes of Q A – Q B → Q A Q B – electron transfer were ΔG 0 = –57 meV, –69 meV, –85 meV for the wild-type and ΔG 0 = 0 meV, –15 meV, –46 meV for the mutant at pH = 8.0, in detergent, liposome and ICM, respectively. The differences in the stabilization energies of both strains decreased from the detergent via proteoliposome to chromatophore. We conclude that the energetics of the interquinone electron transfer depends on the environment of the reaction center. The steric and/or electrostatic interactions of the environment and Q B pocket can modulate the energetics of the charge stabilization over large distances. The interaction may have crucial importance on coupling the electron transport in the photosynthetic membrane to the anabolic/catabolic processes taking place in the cells.


1991 ◽  
Vol 46 (11-12) ◽  
pp. 1059-1062 ◽  
Author(s):  
Walter Oettmeier ◽  
Silvana Preuße ◽  
Michael Haefs

Thiazolylidene-ketonitriles are efficient inhibitors of photosynthetic electron flow in reaction centers from either Rhodobacter sphaeroides or Rhodobacter capsulatus. Some compounds of this class exhibit a higher inhibitory potency in the bacterial system as compared to photosystem II. Up to now, photosystem II inhibitors were generally less active in photosynthetic bacteria. An azido-thiazolylidene-ketonitrile upon illumination almost exclusively tags the L-subunit in the bacterial reaction center.


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