The nanoparticles production was expressed with an absorption peak at 420 nm in UV–Vis spectrum corresponding to the Plasmon resonance of silver nanoparticles thus confirming their presence. The Fourier transform selleckchem infrared spectroscopy confirmed the presence of protein as stabilizing agent surrounding the silver nanoparticles.29

In another report the bacterial Pseudomonas sp isolated from marine sample was cultured and treated with silver nitrate for synthesis of silver nanoparticles. Silver nanoparticles were obtained intracellularly which was characterized by UV-Spectrophotometer, X-Ray diffraction, and Scanning electron microscopy revealed the silver nano particles displayed poly dispersed with different sizes are ranging from 20 to 100 nm in size. XRD analysis showed that these nanoparticles

exhibit a face-centered cubic crystal structure. 30 Similarly marine microalgae was collected from Central Marine Fisheries Research Institute and cultured in the laboratory and challenged with silver nitrate resulted in fabrication of silver nanoparticles LY2835219 ic50 by normal and microwave irradiation technique and the synthesized nanoparticles were evaluated for antimicrobial activity against human pathogens The production of silver nanoparticle was confirmed by UV–Vis spectroscopy at 420 nm by the presence of Plasmon peak. Further confirmation was done by scanning electron microscope (SEM). These results not only provide a base for further research but still useful for drug development in the present and future.31 Yet another report performed by employing marine yeast Candida sp. VITDKGB isolated from Nicobar Islands, India. Production of silver nanoparticles was confirmed by the absorption peak at 430 nm in UV–Vis spectroscopy due to the surface Plasmon resonance of silver nanoparticles. Nanoparticles synthesized were characterized by atomic force

microscopy, Fourier transform infrared spectroscopy and X-ray diffraction. The nanoparticles were evaluated for antimicrobial activity against multi drug resistant microorganism. 32 Similarly extracellular biosynthesis of silver nanoparticles was reported by employing marine cyanobacterium, Oscillatoria willei NTDM01 which reduces silver ions and stabilizes most the silver nanoparticles by a secreted protein. The silver nitrate solution incubated with washed marine cyanobacteria resulted in formation of silver nanoparticles. The characteristics of the protein shell at 265 nm were observed in Ultra violet spectrum for the silver nanoparticles in solution. While FTIR analysis confirmed the presence of a protein shell which are responsible for the nanoparticles biosynthesis. Scanning electron microscopy studies revealed that the formation of agglomerated silver nanoparticles due to the capping agent in the range of 100–200 nm.