[ATP pool and bioluminescence in psychrophilic bacteria Photobacterium phosphoreum].

Bioluminescence activity and ATP pool were investigated in the culture of psychrophilic bacteria Photobacterium phosphoreum collected-from the exponential and stationary growth phases, as well as immobilized in polyvinyl alcohol (PVA) cryogel. In liquid culture, ATP pool remained at an almost a constant level throughout the luminescence cycle (over 100 h). The ATP pool in the stationary-phase and PVA-immobilizedl cells remained constant throughout their incubation in the medium (over 200 h) and in 3% NaCl solution (over 100 h): Quantitative assessment of integral photon yield and ATP pool indicated that bioluminescence decay in growing or stationary cells was not caused by limitation by the energy substrates of the luciferase reaction. Kinetic and quantitative parameters of emission activity and ATP pool excluded the possibility of formation of the aldehyde substrate for luciferase via reduction of the relevant fatty acids in NADPH and ATP-dependent reductase reaction and its oxidation in the monooxygenase reaction. Our results indicate that the aliphatic aldehyde is not utilized in the process of light emission.

[Effect of light-isotope water on growth of bacterial culture].

The stimulating effect of light-isotope water on microbial growth was demonstrated in bacterial culture Pseudomonas esterophilus. Nutrient medium was prepared of mineral salts and ethyl acetate as a source of carbon dissolved in light-isotope water with ppm 35 and 70; the control medium contained same components dissolved in distilled water. The investigation showed an increase in the number of bacterial cells in the exponential stage of growth in static culture in light-isotope water as compared with the control. Specifically, accretion made up 87.3 and 35.2% in light-isotope water with ppm 35 and 70, respectively. In an hour, the number of cell divisions increased by 6.7% and 3.3%, respectively. Therefore, light-isotope water stimulates the metabolic activity and, consequently, growth of bacterial cells.