The use of biologically derived metal nanoparticles for various proposes is going to be an issue of considerable importance; thus, appropriate methods should be developed and tested for the biological synthesis and recovery of these nanoparticles from bacterial cells. In this research study, a strain of Klebsiella pneumoniae was tested for its ability to synthesize elemental selenium nanoparticles from selenium chloride. A broth of Klebsiella pneumoniae culture containing selenium nanoparticles was subjected to sterilization at 121 o C and 17 psi for 20 minutes. Released selenium nanoparticles ranged in size from 100 to 550 nm, with an average size of 245 nm. Our study also showed that no chemical changes occurred in selenium nanoparticles during the wet heat sterilization process. Therefore, the wet heat sterilization process can be used successfully to recover elemental selenium from bacterial cells.
Organic salts of bismuth are currently used as antimicrobial agents against Helicobacter pylori. This study evaluated the antibacterial effect of elemental bismuth nanoparticles (Bi NPs) using a serial agar dilution method for the first time against different clinical isolates and a standard strain of H. pylori. The Bi NPs were biologically prepared and purified by a recently described method and subjected to further characterization by infrared spectroscopy and anti-H. pylori evaluation. Infrared spectroscopy results showed the presence of carboxyl functional groups on the surface of biogenic Bi NPs. These biogenic nanoparticles showed good antibacterial activity against all tested H. pylori strains. The resulting MICs varied between 60 and 100 μg/ml for clinical isolates of H. pylori and H. pylori (ATCC 26695). The antibacterial effect of bismuth ions was also tested against all test strains. The antimicrobial effect of Bi ions was lower than antimicrobial effect of bismuth in the form of elemental NPs. The effect of Bi NPs on metabolomic footprinting of H. pylori was further evaluated by (1)H NMR spectroscopy. Exposure of H. pylori to an inhibitory concentration of Bi NPs (100 μg/ml) led to release of some metabolites such as acetate, formic acid, glutamate, valine, glycine, and uracil from bacteria into their supernatant. These findings confirm that these nanoparticles interfere with Krebs cycle, nucleotide, and amino acid metabolism and shows anti-H. pylori activity.
During recent years, biological synthesis of nanoparticles by microorganisms has been receiving increasing attention. In this investigation, an antimony-transforming bacterium was isolated from the Caspian Sea in northern Iran and was used for intracellular biosynthesis of antimony sulfide nanoparticles. This isolate was identified as nonpigmented Serratia marcescens using conventional identification assays and the 16S rDNA fragment amplification method, and was used to prepare inorganic antimony nanoparticles. The biogenic nanoparticles were released by liquid nitrogen and extracted using two sequential solvent extraction systems. Different characterizations of the extracted inorganic nanoparticles such as particle shape, size and composition were carried out with different instruments. The energy-dispersive x-ray demonstrated that the extracted nanoparticles consisted of antimony and sulfur atoms. In addition, the transmission electron micrograph showed the small and regular non-aggregated nanoparticles ranging in size less than 35 nm. Although the chemical synthesis of antimony sulfide nanoparticles has been reported in the literature, the biological synthesis of antimony sulfide nanoparticles has not previously been published. This is the first report to demonstrate a biological method for synthesizing inorganic nanoparticles composed of antimony. A simple extraction method for isolation of antimony sulfide nanoparticles from bacterial biomass is also reported in the current investigation.
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