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The last decade has observed a rapid advancement in utilising biological system towards bioremediation of metal ions in the form of respective metal nanostructures or microstructures. The process may also be adopted for respective metal nanoparticle biofabrication. Among different biological methods, bacteria‐mediated method is gaining great attention for nanoparticle fabrication due to their eco‐friendly and cost‐effective process. In the present study, silver nanoparticle (AgNP) was synthesised via continuous biofabrication using Aeromonas veronii, isolated from swamp wetland of Sunderban, West Bengal, India. The biofabricated AgNP was further purified to remove non‐conjugated biomolecules using size exclusion chromatography, and the purified AgNPs were characterised using UV–visible spectroscopy, X‐ray diffraction, field emission scanning electron microscopy and transmission electron microscopy (TEM). Additionally, the presence of proteins as capping and stabilising agents was confirmed by the amide‐I and amide‐II peaks in the spectra obtained using attenuated total reflection Fourier transform infrared spectroscopy. The size of biofabricated AgNP was 10–20 nm, as observed using TEM. Additionally, biofabricated AgNP shows significant antibacterial potential against E. coli and S. aureus. Hence, biofabricated AgNP using Aeromonas veronii, which found resistant to a significant concentration of Ag ion, showed enhanced antimicrobial activity compared to commercially available AgNP. [ABSTRACT FROM AUTHOR]

High‐quality colloidal silver nanoparticles (AgNP) were synthesised via a green approach by using hydroalcoholic extracts of Malva sylvestris. Silver nitrate was used as a substrate ion while the plant extract successfully played the role of reducing and stabilising agents. The synthesised nanoparticles were carefully characterised by using transmission electron microscopy, atomic‐force microscopy, energy dispersive X‐ray spectroscopy, Fourier transform infrared spectroscopy and UV–vis spectroscopy. The maximum absorption wavelengths of the colloidal solutions synthesised using 70 and 96% ethanol and 100% methanol, as extraction solvents, were 430, 485 and 504 nm, respectively. Interestingly, the size distribution of nanoparticles depended on the used solvent. The best particle size distribution belonged to the nanoparticles synthesised by 70% ethanol extract, which was 20–40 nm. The antibacterial activity of the synthesised nanoparticles was studied on Escherichia coli, Staphylococcus aureus and Streptococcus pyogenes using disk diffusion, minimum inhibitory concentrations and minimum bactericidal concentrations assays. The best antibacterial activity obtained for the AgNPs produced by using 96% ethanolic extract. [ABSTRACT FROM AUTHOR]

Biological routes of synthesising metal nanoparticles (NPs) using microbes have been gaining much attention due to their low toxicity and eco‐friendly nature. Pseudomonas aeruginosa JP2 isolated from metal contaminated soil was evaluated towards extracellular synthesis of silver NPs (AgNPs). Cell‐free extract (24 h) of the bacterial isolate was reacted with AgNO3 for 24 h in order to fabricate AgNPs. Preliminary observations were recorded in terms of colour change of the reaction mixture from yellow to greyish black. UV‐visible spectroscopy of the reaction mixture has shown a progressive increase in optical densities that correspond to peaks near 430 nm, depicting reduction of ionic silver (Ag+) to atomic silver (Ag0) thereby synthesising NPs. X‐ray diffraction spectra exhibited the 2θ values to be 38.4577° confirming the crystalline and spherical nature of NPs [9.6 − 26.7 (Ave. = 17.2 nm)]. Transmission electron microscopy finally confirmed the size of the particles varying from 5 to 60 nm. Moreover, rhamnolipids and proteins were identified as stabilising molecules for the AgNPs through Fourier transform‐infrared spectroscopy. Characterisation of bacterial crude and purified protein fractions confirmed the involvement of nitrate reductase (molecular weight 66 kDa and specific activity = 3.8 U/mg) in the Synthesis of AgNPs. [ABSTRACT FROM AUTHOR]

Extracellular and intracellular biosynthesis of silver nanoparticles (AgNPs) by Euglena gracilis (EG) strain and Euglena intermedia (EI) strain are reported in this study. The obtained nanoparticles showed an absorption peak approximates 420 nm in the UV–visible spectrum, corresponding to the plasmon resonance of AgNPs. According to the result of inductively coupled plasma‐atomic emission spectrometer, the intakes of silver ions by EI and EG are roughly equal. The transmission electron microscope (TEM) analysis of the successful in vivo and in vitro synthesised AgNPs indicated the sizes, ranging from 6 to 24 nm and 15 to 60 nm in diameter, respectively, and a spherical‐shaped polydispersal of the particles. The successful formation of AgNPs has been confirmed by energy dispersive X‐ray analysis connected to the TEM. The Fourier transform infrared spectroscopy measurements reveal the presence of bioactive functional groups such as amines are found to be the capping and stabilising agents of nanoparticles. To our knowledge, this is the first report where two kinds of Euglena microalga were used as the potential source for in vivo and in vitro biosynthesis of AgNPs. [ABSTRACT FROM AUTHOR]

Stable aqueous monodispersed silver nanoparticles were synthesised by reducing silver nitrate using various sugars such as glucose, fructose, lactose, and sucrose at 55-60 °C. A mixture of two stabilising agents, polyvinyl pyrrolidone (PVP) of molecular weight (MW 40, 000) and gelatin plays a decisive part in controlling size and shape of superfine silver nanoparticles. Using PVP, better control of particle size was obtained, whereas a mixture of PVP, and gelatin resulted in sea urchin kind of structure. Effects of several processing parameters such as pH, quantities of alkaline solution, reaction time, concentration of stabilising agent, and the metal/dispersant ratio were investigated. The suspensions were stable for at least one week. Silver nanoparticles can be easily collected by centrifugation on mixing with sufficient amount of acetone. Structural characterisation of synthesised silver nanoparticles was carried out by X-ray diffraction (XRD), which shows that the as-synthesised silver nanoparticles are face-centered cubic crystalline. Chemical characterisations of as-synthesized silver nanoparticles were done using inductively-coupled plasma-optical emission spectrometry (ICP-OES) and LECO gas analysers. The optical properties of silver nanoparticles were monitored using UV-Vis spectrophotometer. Role of stabilising agent in protecting the silver nanoparticles was studied using fourier transform infrared spectroscopy (FTIR). Particle size and distribution were characterised using small-angle X-ray scattering (SAXS), zeta particle size analyser (PSA), scanning electron microscopy, and transmission electron microscopy. The average particle size of the as-synthesised silver nanoparticles was 35 nm. [ABSTRACT FROM AUTHOR]