Production and purification of antioxidant peptides from a mungbean meal hydrolysate by Virgibacillus sp. SK37 proteinase

Antioxidant peptides of mungbean meal hydrolysed by Virgibacillus sp. SK37 proteinases (VH), Alcalase (AH) and Neutrase (NH) were investigated. The antioxidant activities based on 2,2′-azinobis (3-ethyl-benzothiazoline-6-sulphonate) (ABTS) radical-scavenging, ferric-reducing antioxidant power (FRAP) and metal chelation of VH were comparable to those of NH. VH was purified using ultrafiltration, ion exchange and gel filtration chromatography. The purified peptides (F37) from VH, which had the highest specific antioxidant activity, consisted of four peptides containing an arginine residue at their C-termini. In addition, the ABTS radical-scavenging activity of the purified peptides (F42) at 0.148 mg/ml was comparable to that of 1 mM of butylated hydroxytoluene (BHT). These two fractions were stable over a wide pH (4–10) and temperature (25–121 °C) range. Virgibacillus sp. SK37 proteinase is a potential processing-aid for the production of a mungbean meal hydrolyzate with antioxidant properties.     

Spent brewery yeast sludge as a single nitrogen source for fibrinolytic enzyme production of Virgibacillus sp. SK37

The objectives of this study were to investigate the suitable food industrial byproducts and conditions affecting proteinase production of Virgibacillus sp. SK37 as well as to evaluate fibrinolytic activity of secreted proteinases. Among 5 food industrial wastes including soybean pomace, rice bran, mungbean protein, spent brewery yeast sludge (Ys), and fish sauce sludge, Ys was the best nitrogen source for proteinase production from Virgibacillus sp. SK37. The highest level of proteinase production was obtained in the medium containing 1% Ys, 2.5% NaCl, pH 7.5 at 40°C, which was about 1.7 times higher than the commercial yeast extract medium. Virgibacillus sp. SK37 proteinases completely hydrolyzed fibrinogen within 50 min with Aα-chain being the first target and followed by Bβ- and Γ-chains. Virgibacillus sp. SK37 could be a potential source of fibrinolytic enzyme that can be developed as a functional food ingredient.