Preparation of Antioxidant Peptides from Salmon Byproducts with Bacterial Extracellular Proteases

• Published in: Marine drugs Vol. 15; no. 1; p. 4
• Main Authors: Wu, Ribang, Chen, Leilei, Liu, Dan, Huang, Jiafeng, Zhang, Jiang, Xiao, Xiao, Lei, Ming, Chen, Yuelin, He, Hailun
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 11.01.2017; MDPI
• Subjects: Animals; antioxidant peptide; Antioxidants - chemistry; Bacteria; bacterial extracellular proteases; Bacterial Proteins - chemistry; Chromatography, Gel - methods; enzymatic hydrolysis; evaluation of antioxidant activity; Hydrolysis; Hydroxyl Radical - chemistry; Marine; Peptide Hydrolases - chemistry; peptide purification; Peptides - chemistry; Protein Hydrolysates - chemistry; Pseudoalteromonas; Salmon - metabolism; Salmonidae; antioxidant peptide; peptide purification; bacterial extracellular proteases; evaluation of antioxidant activity; enzymatic hydrolysis
• ISSN: 1660-3397; 1660-3397
• DOI: 10.3390/md15010004

Bacterial extracellular proteases from six strains of marine bacteria and seven strains of terrestrial bacteria were prepared through fermentation. Proteases were analyzed through substrate immersing zymography and used to hydrolyze the collagen and muscle proteins from a salmon skin byproduct, respectively. Collagen could be degraded much more easily than muscle protein, but it commonly showed weaker antioxidant capability. The hydrolysate of muscle proteins was prepared with crude enzymes from sp. SQN1 displayed the strongest activity of antioxidant in DPPH and hydroxyl radical scavenging assays (74.06% ± 1.14% and 69.71% ± 1.97%), but did not perform well in Fe chelating assay. The antioxidant fractions were purified through ultrafiltration, cation exchange chromatography, and size exclusion chromatography gradually, and the final purified fraction U2-S2-I displayed strong activity of antioxidant in DPPH, hydroxyl radical scavenging assays (IC = 0.263 ± 0.018 mg/mL and 0.512 ± 0.055 mg/mL), and oxygen radical absorption capability assay (1.960 ± 0.381 mmol·TE/g). The final purified fraction U2-S2-I possessed the capability to protect plasmid DNA against the damage of hydroxyl radical and its effect was similar to that of the original hydrolysis product. It indicated that U2-S2-I might be the major active fraction of the hydrolysate. This study proved that bacterial extracellular proteases could be utilized in hydrolysis of a salmon byproduct. Compared with collagen, muscle proteins was an ideal material used as an enzymatic substrate to prepare antioxidant peptides.