The Sporobolomyces salmonicolor AL(1) Antarctic strain was cultivated and two bioproducts were obtained: exopolysaccharide and biomass. The biologically active substances ergosterol, torularhodin, torulene, β-carotene and CoQ(10) were extracted from the biomass and were quantified as follows: ergosterol 5.2 ± 0.2 mg/g, torularhodin 458.3 ± 24.5 μg/g, torulene 273.7 ± 14.5 μg/g, β-carotene 129.2 ± 7.3 μg/g and coenzyme Q(10) (CoQ(10)) 236.1 ± 12.1 μg/g. Their antioxidant activity was estimated according to the cathode voltammetry method. The most pronounced antioxidant activity (according to trolox) was exhibited by β-carotene 3.78, followed by CoQ(10) 3.60, both of them being the main contributors to the total extract activity of 3.19. The biologically active metabolites in combination with exoglucomannan as emulsifier were used for the creation of model emulsion systems characterised by great stability. The absorption of UVA rays by the model emulsions was studied.
The fluorescence analysis of Escherichia coli (E. coli) bacteria was done. It has been established that a luminescent signal from the one of metabolites (reduction form of nicotinamide adenine dinucleotide, NADH) can be adopted as a vitality indicator of the bacteria. This signal was chosen as an analytical signal. It was determined that the nature of this signal is fluorescence. In order to eliminate influence of the light scattering on this fluorescence signal optimal conditions were chosen
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