Green synthesis of silver nanoparticles using the seaweed Gracilaria birdiae and their antibacterial activity

AbstractThis work presents a simple method for the green synthesis of silver nanoparticles (AgNPs) using as reducing and stabilizing agent a polysaccharide extracted from red algae Gracilaria birdiae present in the coast of Piauí. The AgNPS were prepared using three polysaccharide concentrations (0.02, 0.03 and 0.05% v/v) and two pHs (10 and 11) at stirring for 30min at 90°C. The formation of silver nanoparticles was monitored by measurements of UV–vis and FTIR and characterized by size and zeta potential measurements using DLS and morphologically by TEM. The UV–vis absorption spectrum showed the surface plasmon peak at 410nm, which is characteristic peak of silver nanoparticles. The functional biomolecules present in the polysaccharide and the interaction between the nanoparticles were identified by the Fourier transform infrared spectroscopy (FTIR) analysis. The stability of the synthesized silver nanoparticles was analyzed during four months and no significant agglomeration was observed. The hydrodynamic diameter of the AgNPs varied between 20.2nm and 94.9nm. The AgNPs were tested for antimicrobial activity using Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive) and all samples showed antimicrobial activity against E. coli. Using an environment-friendly, the AgNPs were synthesized in a simple, rapid and one-step process using natural sources as red algae with favorable characteristics such as spherical shape, small size and zeta potential negative. The results suggest that the polysaccharide mediated synthesized silver nanoparticles could be used as a model for future projects of nano-medicines or drug delivery systems

Characterization and Biological Activities of Ocellatin Peptides from the Skin Secretion of the Frog Leptodactylus pustulatus

Eight new peptides were isolated from the skin secretion of the frog Leptodactylus pustulatus and their amino acid sequences determined by de novo sequencing and by cDNA cloning. Structural similarities between them and other antimicrobial peptides from the skin secretion of Leptodactylus genus frogs were found. Ocellatins-PT1 to -PT5 (25 amino acid residues) are amidated at the C-terminus, while ocellatins-PT6 to -PT8 (32 amino acid residues) have free carboxylates. Antimicrobial activity, hemolytic tests, and cytotoxicity against a murine fibroblast cell line were investigated. All peptides, except for ocellatin-PT2, have antimicrobial activity against at least one Gram negative strain. Ocellatin-PT8 inhibited the growth of Escherichia coli, Staphylococcus aureus, Klebsiella pneumoniae, and Salmonella choleraesuis strains with MICs in the 60−240 μM range. No significant effect was observed in human erythrocytes and in a murine fibroblast cell line after exposure to the peptides at MICs. A comparison between sequences obtained by both direct HPLC-MS de novo sequencing and cDNA cloning demonstrates the secretion of mature peptides derived from a pre-pro-peptide structure