Treatment with humic substances (preparation Biomin) considerably increased viability of algae during long storage (6 months) in collection. The effect was greater with green algae ( Scenedesmus and Chlorella ) than with blue-green algae ( Nostoc and Anabaena ). In intensive cultures, lower Biomin concentrations (1 − 10 mg/l) increased the biomass production, protein, chlorophyll and carotenoid content, as well as α -esterase and glutamate dehydrogenase activities, whereas the lipid and carbohydrate content was higher at 100 mg/l Biomin. A high Biomin concentration (1 g/l) exerted an inhibition. Biomin supply to the cultures in outdoor installation of Shetlik type was associated with a moderate stimulation of algal biomass accumulation. It was concluded that Biomin might be helpful in the improvement of algal viability and growth.

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The present paper describes the isolation, physiological and genetic characteristic of a bacterial agent which inhibits the growth of algae and causes death of laboratory cultures of Antarctic microalgal strains: prokaryotic cyanobacteria Synechocystis salina and green eukaryotic microalga Choricistis minor. The bacterial strain LB1 was isolated from algal damaged laboratory cultures of S. salina. It was established that this bacterium is obligate aerobic, Gram-positive, non-spore-forming, immotile, irregular rods with dimensions 0.3-2 μm. Our results showed that LB1 has algicidal effect to S. salina as well as to C. minor. Transmission electron microscopy observations confirmed the destruction of S. salina by the bacterium. Biochemical analysis of LB1 revealed positive reaction to D-glucose, catalase, hydrolysis of gelatin, acid production from: lactose, L-arabinose, L-ramnose, esculin and β-galactosidase. The partial sequence (1,404 bp) of the 16S rRNA gene of LB1 showed 99 % similarity with type strains of the genus Microbacterium. The results of the biochemical, antimicrobial and of 16S rRNA analysis of LB1 allowed us to identify LB1 as Microbacterium sp. Studying expression of pathogenicity of the bacteria to algal cultures will help to solve the problem of algal production for biotechnological purposes.