[Use of hydropyrite in the chemiluminescent determination of iron-porphyrin proteins]. / Primenenie gidropirita v reaktsiiakh khemiliuminestsentnogo opredeleniia zhelezoporfirinovykh belkov

Hydropyrite was found to be a suitable reagent which may be used in chemiluminescent reactions for determination of iron-porphyrin proteins.

[Effect of nitrogen source on growth of Arthrobacter simplex and its biosynthesis of cholinesterase]. / Vliianie istochnika azota na rost Arthrobacter simplex i biosintez kholinésterazy

The effect of organic and inorganic forms of nitrogen on biomass accumulation and cholinesterase synthesis was studied with Arthrobacter simplex var. cholinesterasus. The culture assimilates nitrogen of ammonium compounds better than other forms of inorganic nitrogen; the best nitrogen source for biosynthesis of cholinesterase is ammonium phosphate. Nitrogen of nitrates is not assimilated. The amount of biomass is almost twice as high on the medium with peptone, casein or casein hydrolysate as on the medium with mineral nitrogen, while the activity of cholinesterase on these nitrogen sources decreases 1.5--2.0 times. Yeast extract as a nitrogen source increases biomass accumulation by a factor of 2.5 and does not supress synthesis of cholinesterase. The concentration of the enzyme synthesized per unit biomass on the medium with yeast extract is the same as on the medium containing ammonium phosphate. The effect of amino acids and amides, i.e. beta-alanine, proline, amides of aspartic and glutamic acids, and their mixtures, is similar to the action of yeast extract: they stimulate biomass accumulation and do not inhibit synthesis of the enzyme. Other amino acids supress synthesis of cholinesterase. The amount of accumulated biomass in the presence of glutamic acid is twice as high as in the case of any other amino acid, and three times as high as on the medium containing ammonium phosphate. Similar action of glutamic acid is manifested when it is used in mixtures with other amino acids. On the medium containing glutamic acid as a sole source of nitrogen, an increase in biomass production is accompanied with a decrease in biosynthesis of the enzyme by 50%. Repression of the biosynthesis is less if glutamic acid is added in mixtures with proline, beta-alanine and asparagine.

[Radiometric study of the decarboxylating activity of desert soil microflora]. / Issledovani dekarboksiliruiushchei aktivnosti mikroflory pustynnykh pochv radiometricheskim metodom

Employment of growth media containing salts of organic acids, labelled with 14C, gave a rapid and intensive signal concerning the decarboxylating activity of microorganisms from desert soils. The value of the signal was higher than that during the decomposition of uniformly labelled glucose. The results of these studies would help to select the optimal growth medium for carrying out exobiological experiments.

[Activity of microorganisms decomposing cholesterol]. / Ob aktivnosti mikroorganizmov, razlagaiushchikh kholesterin

The rates of cholesterol decomposition was compared among cell suspensions of different microorganisms. Fifty seven cultures were studied: 2 strains of actinomycetes, 23 strains of proactinomycetes, 22 strains of mycobacteria, and 10 strains of bacteria. During four hours of incubation, 11 strains virtually did not decompose cholesterol at all, 10 strains decomposed it by up to 20 per cent, 21 strains by 20 to 70 per cent, and 15 strains by 70 to 100 per cent. The highest activity was displayed by Mycobacterium rubrum 297 and Mycobacterium sp. 2B, which decomposed all cholesterol in the sample within 4 hours. The high activity was also displayed by Proactinomyces sp. 2006, Nocardia opaca JMET 7030, and Nacardia erythropolis JMET 7252.

[Decomposition of cholesterol by Achromobacter candicans]. / Razlozhenie kholesterina Achromobacter candicans

The decomposition of cholesterol by the cell suspensions of Achromobacter candicans 42 and by the cell-free extracts of this bacterium was studied. The decomposition of cholesterol in the presence of the wet biomass during four hours of the incubation was 72.5 percent, and with the cells that were preliminarily lyophilized or treated by acetone 49.8 and 23.0 percent, respectively. The activity decreased from 70.0 to 50.0 percent if the biomass was kept at minus 3 degrees C during 70 days. The decomposition of cholesterol by the cell-free preparations (supernatant and protein after precipitation with ammonium sulphate to 0.7 saturation) constituted 40.0 percent of the cholesterol contained in a sample. One of the intermediate products of cholesterol decomposition was delta4-cholesten-3-one.