Abstract
Measurement of the electrical potential difference (Δψ) in membrane vesicles (chromatophores) from the purple bacterium Rhodobacter sphaeroides, associated with the surface of a nitrocellulose membrane filter (MF), impregnated with phospholipid solution in decane, as well as immersed inside it, in the presence of exogenous mediators and disaccharide trehalose, demonstrated an increase in the amplitude and stabilization of the signal under continuous illumination. The ascorbate/N,N,N′N′-tetramethyl-p-phenylenediamine pair and ubiquinone-0 were used as mediators (electron donor and acceptor), respectively. Although the stabilization of photoelectric responses under long-term continuous illumination was observed in both cases of immobilization of chromatophores, only when the samples were immersed inside the MF, the functional activity of the reaction centers was maintained for a month when they were stored in the dark at room temperature. Stable photoresponses are probably associated with the preservation of the integrity of chromatophore proteins inside MF pores. The stabilizing effect of the bioprotector trehalose may be due to both its effect on RC proteins and on the phospholipid bilayer membrane. The results obtained will expand modern ideas about the use of semi-synthetic structures based on various intact photosynthetic systems capable of converting solar energy into an electrochemical form.
Published Version
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