7 Common human pathogenic bacterial strains such as Staphylococcus aureus, Enterococcus faecalis, Klebsiella pneumoniae and Serratia marcescens were used for assessing the antimicrobial potential and geno-toxic nature of SNPs synthesized in the laboratory. The strains were obtained from SRM Medical College, Rigosertib nmr Chennai and were cultured at 35 °C on Mueller–Hinton agar. The SNPs were prepared according to the procedure described in the literature.7 and 8 In brief, 24 h old culture of B. subtilis A1 was used

as inoculum and grown in LB broth. Cultivations were performed and incubated at 30 °C for 18 to 20 h on a rotatory shaker at 150 r min−1 and the cells harvested by centrifugation and the supernatant was used for the synthesis of SNPs using 1 mM AgNO3 prepared using Milli-Q Vemurafenib datasheet water (Milli-Q Integra 3, Millipore, MA). The experiment was run along with control and the flasks incubated on a rotatory shaker at 150 rpm in dark condition at 30 °C. Shimadzu UV-1800 UV–visible spectrophotometer was used to monitor the optical measurements by random sampling of 2 mL aliquot of the reaction mixture in the range

200–800 nm at a resolution of 1 nm. The X-ray diffraction patterns were recorded on a Rigaku multiflex diffractometer using Cu-Kβ radiation (λ = 0.1542 nm) operated at 40 kV and 100 mA. The experiments were performed in the diffraction angle range of 2θ = 20−80°. The morphology and elemental composition of the SNPs were analysed by field emission scanning electron microscopy (FESEM) and energy dispersive spectroscopy (EDX) using a 10 KeV Hitachi S-3000H microscope. The bactericidal activity of SNPs was determined by performing Kirby Bauer’s disc diffusion method. Log phase bacterial inoculums also (108 cfu/mL) were standardized using McFarland’s standard and were uniformly spread over MHA plate using a sterile swab (HiMedia, India). SNPs of various concentrations (5 μg, 10 μg, 15 μg, 20 μg/mL) were prepared and adsorbed onto sterile discs. The discs were then carefully placed on the MHA plates

and incubated at 37 °C for 24 h. Control discs were run using culture filtrate and aqueous silver nitrate. The geno-toxic study was performed on the genomic DNA extracted from the clinical strains by alkali lysis method.9 The DNA extracted was made in aliquots of 10 μg/mL tris Modulators acetate buffer (pH 8.0) and stored at −20 °C. The aliquots of SNPs were added separately to the purified DNA samples and incubated at 37 °C for 6 h and 12 h respectively. Gel Electrophoresis was carried out using 1% agarose prepared in tris acetate buffer and stained with 0.5 μg/mL ethidium bromide. The set up was run at 100 Amp for 30 min after which the gel was visualized in a Gel documentation system. The extracellular synthesis of SNPs using the culture supernatant of B. subtilis A1 was observed.