With this, the master colloidal solution contains an aqueous solu

With this, the master colloidal solution contains an aqueous solution of molybdenum nanoparticles with concentration of not less than 8 mg/l. The size of nanoparticles of metals

is from 100 to 250 nm and their concentration in bidistilled water is not more than the value calculated by formula 1. (1) where m is the concentration of nanoparticles of metal (mg/l) and V is the volume of 1 mole of metal atoms (cm3/mol). The colloidal solution of nanoparticles of molybdenum was used in the dose of 1 microliter per gram (μl/g). Microbial preparation check details used in our experiments is registered in Ukraine trademark and is included into the list of pesticides and agrochemicals permitted for use in Ukraine. As an active agent, the highly competitive strains of Bradyrhizobium japonicum were used, adapted to the soil and climatic conditions of Ukraine. The concentration of bacteria in 1 g of preparation is not less than 6 × 108 cells. The preparation was used in accordance to the manufacturer’s instructions in a dose of 200 g per 1.2 l of water per hectare of seed rate that corresponds to 106 of bacteria cell concentration per

single seed. Experiments were performed in stationary conditions at the Agronomy Department of Plant Experimental Station of National University of Life and Environmental Sciences of Ukraine on typical gray, light sandy loam soils. Chickpea seed inoculation was carried out for 1 to 2 h before sowing. The seeds were dampened with water (2% Selleckchem YH25448 by weight) in control variant, aqueous suspension

of microbial preparation, colloidal solution of molybdenum nanoparticles alone and in combination with microbial preparation. The scheme of the experiment is as follows: 1. Control (water treatment)   2. Colloidal solution of nanoparticles Tyrosine-protein kinase BLK of molybdenum (CSMN)   3. Microbial preparation   4. Microbial preparation + CSMN   Determination and quantification of basic physiological groups of microorganisms in rhizosphere soil of chickpea plants was performed using standard microbiological methods [14]. Sowing of microorganisms on culture media are made of 10−3 dilutions (fungi and cellulose destructive bacteria) and 10−4 (other microorganisms). Sowing of each dilution was performed at least three times. Calculation of the total number of microorganisms on nutrient media was performed on the third, fifth, and seventh day of incubation. After counting the number of colonies on the surface, the number of microorganisms in 1 ml of the appropriate dilution was determined. In the estimation of the number of cells of microorganisms in 1 g of wet soil, the result obtained was multiplied by the degree of dilution (103, 104, 105, etc.). To determine the number of microorganisms in 1 g of dry soil, the respective number of cells in 1 g of wet soil was multiplied by a correction factor of soil moisture [12, 14].

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