The pellet was treated with two different buffers (A and B) for suspension of insoluble aggregates. Buffer A (6 M Gua–HCl, 300 mM sodium chloride, 50 mM sodium phosphate (pH 7.4) and 20 mM imidazole) and buffer B (8 M urea, 300 mM sodium chloride and 20 mM imidazole) in order to identify the fraction soluble or insoluble

in which the peptide is located. The suspensions containing soluble peptides were centrifuged at 4500 × g at 4 °C for 15 min and the pellet was resuspended in100 μL of distilled water. Protein purification was performed by immobilized metal ion affinity chromatography (IMAC) in a Nickel His-Trap 1 mL column (GE, Upsala) using imidazole in binding buffer (20 mM imidazole) and eluted with imidazole elution Staurosporine buffer (500 mM Imidazole). The clarified lysate was placed in affinity column Crude His Nintedanib price Trap FF crude columns 1 mL (GE) for purification according to the manufacturer’s instructions. Protein samples were electrophoresed in Tricine–SDS-PAGE (16%) under non-denaturating

conditions as described by Schagger [34] with minor modifications. Protein quantification was carried out according to Lowry [22] and BSA (bovine serum albumin) was used as the standard. The Pg-AMP1 (50 μg) was mixed with sample buffer Electrophoresis was performed in the Mini-PROTEAN Tetra Electrophoresis System® (Bio-Rad). Peptides were fixed and further silver stained. Ultra low range molecular weight marker (1.6–26.6 kDa) from Sigma™ and protein marker (2–212 kDa) (New England Biolabs, Ipswich, MA) was used as standard. Tris-Tricine–SDS-PAGE gel was electro-blotted for 20 min at 100 V onto an RPN3032D (0.20 μm pore size) nitrocellulose membrane (Amersham Hybond-ECL/GE). Aldol condensation Membrane was washed in

PBS and blocked by immersing the membrane in PBS-T 0.1%. The membrane was primarily incubated with anti-His antibody (GE) (1:1000) overnight then washed in PBS-T and incubated with the secondary antibody (1:1000) diluted in PBS with 3% antibody anti-mouse IgG peroxidase conjugate (GE) added for 1 h at room temperature detection was carried out in a dark room using Amersham ECL Prime Western Blotting Detection Reagent (GE) on auto radiography film (Amersham Hyperfilm ECL). Antimicrobial activities of recombinant purified Pg-AMP1 were tested against the after mentioned Gram-negative and Gram-positive bacteria. Polypropylene microplates were used to inoculate 100 μL of TSB medium containing the microorganism (concentration of 5 × 104 CFU mL−1 well−1) and 100 μL of Pg-AMP1 recombinant peptide dissolved in saline solution (0.9 g L−1) at different concentrations (25, 50 and 100 μg mL−1) to determine the minimal inhibitory concentration (MIC). Two sets of negative control were used: (I) bacteria treated with wash buffer 20 mM sodium phosphate, 500 mM imidazole, sodium 0.5 M chloride (pH 7.4); (II) saline solution (0.9 g L−1). Chloramphenicol was used as positive control at 1000, 100, 50 and 25 μg mL−1 dissolved in saline solution (0.9 g L−1).