The bacterial action of gentamicin and that of a mixture of gentamicin and 15-nm colloidal-gold particles onEscherichia coliK12 was examined by the agar-well-diffusion method, enumeration of colony-forming units, and turbidimetry. Addition of gentamicin to colloidal gold changed the gold color and extinction spectrum. Within the experimental errors, there were no significant differences in antibacterial activity between pure gentamicin and its mixture with gold nanoparticles (NPs). Atomic absorption spectroscopy showed that upon application of the gentamicin-particle mixture, there were no gold NPs in the zone of bacterial-growth suppression in agar. Yet, free NPs diffused into the agar. These facts are in conflict with the earlier findings indicating an enhancement of the bacterial activity of similar gentamicin–gold nanoparticle mixtures. The possible causes for these discrepancies are discussed, and the suggestion is made that a necessary condition for enhancement of antibacterial activity is the preparation of stable conjugates of NPs coated with the antibiotic molecules.

Plant-growth-promoting rhizobacteria exert beneficial effects on plants through their capacity for nitrogen fixation, phytohormone production, phosphate solubilization, and improvement of the water and mineral status of plants. We suggested that these bacteria may also have the potential to express degradative activity toward glyphosate, a commonly used organophosphorus herbicide. In this study, 10 strains resistant to a 10 mM concentration of glyphosate were isolated from the rhizoplane of various plants. Five of these strains--Alcaligenes sp. K1, Comamonas sp. K4, Azomonas sp. K5, Pseudomonas sp. K3, and Enterobacter cloacae K7--possessed a number of associative traits, including fixation of atmospheric nitrogen, solubilization of phosphates, and synthesis of the phytohormone indole-3-acetic acid. One strain, E. cloacae K7, could utilize glyphosate as a source of P. Gas-liquid chromatography showed that E. cloacae growth correlated with a decline in herbicide content in the culture medium (40% of the initial 5mM content), with no glyphosate accumulating inside the cells. Thin-layer chromatography analysis of the intermediate metabolites of glyphosate degradation found that E. cloacae K7 had a C-P lyase activity and degraded glyphosate to give sarcosine, which was then oxidized to glycine. In addition, strain K7 colonized the roots of common sunflower (Helianthus annuus L.) and sugar sorghum (Sorghum saccharatum Pers.), promoting the growth and development of sunflower seedlings. Our findings extend current knowledge of glyphosate-degrading rhizosphere bacteria and may be useful for developing a biotechnology for the cleanup and restoration of glyphosate-polluted soils.

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Microclonal propagation in vitro is being actively used in the production of healthy planting material of food and ornamental plants. However, it needs further improvement to increase the growth rates of microclones in vitro and enhance regenerant survivability ex vitro. A promising approach to this end could be inoculating in vitro-micropropagated plants with plant growth-promoting rhizobacteria, specifically Azospirillum. However, the influence of Azospirillum inoculation on microclone behavior throughout the production process, including plant adaptation ex vitro and food crop productivity, has been underinvestigated. In this study, in vitrogrowing potato (Solanum tuberosum L.) microclones were inoculated with Azospirillum brasilense strain Sp245. The microclones were then grown on in soil in the greenhouse and field, with the experiment lasting for 120 days. Rootassociated bacteria were identified immunochemically, and the mitotic index of root meristematic cells was determined by a cytological method. The plant morphological parameters determined were shoot length, number of nodes per shoot, number of roots per plant, maximal root length, leaf area, percentage of surviving plants in the soil, and tuber yield and weight. Our results show that bacterial inoculation of potato microclones in vitro enhances plant adaptive capacity ex vitro and increases minituber yield. The percent survival index of field-grown inoculated plants was 1.5-fold greater than that of uninoculated plants. The overall tuber weight per plant was more than 30 % greater in the inoculated plants than it was in the control ones. For all cultivars on average, tuber yield per square meter increased by more than 45 % as a result of inoculation in vitro. This study is the first to report that Azospirillum inoculation of potato microclones not only improves the quality of planting material produced in vitro but also significantly increases minituber yield through enhancing plant adaptive capacity in the field.

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In the present study, we identified exopolysaccharides of the harmful phytopathogenic bacterium Pectobacterium atrosepticum SCRI1043 and characterized the molecular structure of these polymers. The synthesis of the target polysaccharides was shown to be induced under starvation conditions. Moreover, intensive accumulation of exopolysaccharides occurred during the colonization by bacteria of the xylem vessels of infected plants, where microorganisms formed specific 3D "multicellular" structures-bacterial emboli. Thus, the identified polymers are likely to be involved in the adaptation and virulence of bacteria of Pectobacterium genus.

No abstract

We evaluated the ability of several strains of the rhizobacterium Paenibacillus polymyxa, differing in the yield and rheological properties of their exopolysaccharides, to form biofilms on abiotic surfaces. Of these strains, P. polymyxa 1465, giving the highest yield of extracellular polysaccharides and the highest kinematic viscosity of the culture liquid and of aqueous polysaccharide solutions, proved to be the most active in forming biofilms on hydrophobic and hydrophilic surfaces. Enzyme-linked immunosorbent assay with rabbit polyclonal antibodies developed to isolated exopolysaccharides of P. polymyxa 1465 and 92 was used to detect P. polymyxa's polysaccharidic determinants in the composition of the biofilm materials.