Optimization of Sorghum Kafirin Extraction Conditions and Identification of Potential Bioactive Peptides

• Published in: BioResearch open access Vol. 9; no. 1; pp. 198 - 208
• Main Authors: Castro-Jácome, Tania P, Alcántara-Quintana, Luz E, Tovar-Pérez, Erik G
• Format: Journal Article
• Language: English
• Published: United States Mary Ann Liebert, Inc 01.09.2020; Mary Ann Liebert, Inc., publishers
• Subjects: Amino acids; Angiotensin-converting enzyme inhibitors; Antioxidants; Biological activity; Chymotrypsin; Enzymes; Ethanol; Gluten; Grain; Identification; Original; Peptidase; Peptides; Peptidyl-dipeptidase A; Proteins; Raw materials; Sodium; Sodium metabisulfite; Sorghum; Subtilisin; Thermolysin; kafirins; bioactive peptides; white sorghum; amyloglucosidase
• ISSN: 2164-7844; 2164-7860; 2164-7860
• DOI: 10.1089/biores.2020.0013

The interest in extracting kafirins (KAF), the main storage protein from sorghum grain has recently increased due to its gluten-free content and the significant scientific evidence showing the health benefits of the bioactive peptides from cereal grains in human diets. The objectives were to obtain the highest percentage of KAF extraction using amyloglucosidase as pretreatment to increase the extraction yield and predict the bioactive peptides in the KAF. In this study, pretreatments with amyloglucosidase increased the extraction yield of KAF compared with extraction methods using only ethanol and sodium metabisulfite. Two protein fragment sequences were identified from KAF extract and were evaluated for potential bioactive peptide using the BIOPEP-UWM database, which suggest that KAF proteins from white sorghum may be considered as good precursors of dipeptidyl peptidase-inhibitor, angiotensin-converting enzyme inhibitor, antioxidant and hypotensive peptides following chymotrypsin, thermolysin, and subtilisin and their combination. Average scores aligned using PeptideRanker confirmed KAF proteins' potential sources of bioactive peptides with over 5 peptides scored over 0.8. In addition, 31 unexplored peptide sequences that could have biological activity were identified. Our results suggest that KAF can be used in the peptide productions with potential biological activity and beyond.