Bovine Hemoglobin Enzymatic Hydrolysis by a New Ecoefficient Process—Part I: Feasibility of Electrodialysis with Bipolar Membrane and Production of Neokyotorphin (α137-141)

• Published in: Membranes (Basel) Vol. 10; no. 10; p. 257
• Main Authors: Abou-Diab, Mira, Thibodeau, Jacinthe, Deracinois, Barbara, Flahaut, Christophe, Fliss, Ismail, Dhulster, Pascal, Nedjar, Naima, Bazinet, Laurent
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 25-09-2020; MDPI
• Subjects: Abattoirs; Acidification; Antiinfectives and antibacterials; Antimicrobial agents; Antimicrobial peptides; Blood; bovine hemoglobin; Chemical agents; Consumption; Electrodes; Electrodialysis; electrodialysis with bipolar membrane; Environmental Sciences; enzymatic hydrolysis; Enzymes; Experiments; Feasibility; Fouling; Hemoglobin; Hydrolysates; Hydrolysis; Interfaces; Life Sciences; Meat; membrane fouling; Membranes; neokyotorphin; Peptides; Preservatives; Proteins; Salts; Canada; United States > US; Japan
• ISSN: 2077-0375; 2077-0375
• DOI: 10.3390/membranes10100257

Neokyotorphin (α137-141) is recognized as an antimicrobial peptide and a natural meat preservative. It is produced by conventional enzymatic hydrolysis of bovine hemoglobin, a major component of cruor, a by-product of slaughterhouses. However, during conventional hydrolysis, chemical agents are necessary to adjust and regulate the pH of the protein solution and the mineral salt content of the final hydrolysate is consequently high. To produce this peptide of interest without chemical agents and with a low salt concentration, electrodialysis with bipolar membrane (EDBM), an electromembrane process recognized as a green process, with two different membrane configurations (cationic (MCP) and anionic (AEM) membranes) was investigated. Hydrolysis in EDBM showed the same enzymatic mechanism, “Zipper”, and allowed the generation of α137-141 in the same concentration as observed in conventional hydrolysis (control). EDBM-MCP allowed the production of hydrolysates containing a low concentration of mineral salts but with fouling formation on MCP, while EDBM-AEM allowed the production of hydrolysates without fouling but with a similar salt concentration than the control. To the best of our knowledge, this was the first time that EDBM was demonstrated as a feasible and innovative technology to produce peptide hydrolysates from enzymatic hydrolysis.