In Vitro Assessment Methods for Antidiabetic Peptides from Legumes: A Review

被引:12
|
作者
Rahmi, Alia [1 ]
Arcot, Jayashree [1 ]
机构
[1] UNSW Sydney, Sch Chem Engn, Food & Hlth Grp, Sydney, NSW 2052, Australia
关键词
legume peptide; starch digestion inhibitor; glucose absorption inhibitor; diabetes management; PHASEOLUS-VULGARIS L; IV INHIBITORY PEPTIDES; ANGIOTENSIN-CONVERTING ENZYME; ALPHA-AMYLASE; BIOACTIVE PEPTIDES; VIGNA-UNGUICULATA; TO-COOK; ANTIOXIDANT ACTIVITIES; FUNCTIONAL-PROPERTIES; PROTEIN HYDROLYSATE;
D O I
10.3390/foods12030631
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Almost 65% of the human protein supply in the world originates from plants, with legumes being one of the highest contributors, comprising between 20 and 40% of the protein supply. Bioactive peptides from various food sources including legumes have been reported to show efficacy in modulating starch digestion and glucose absorption. This paper will provide a comprehensive review on recent in vitro studies that have been performed on leguminous antidiabetic peptides, focusing on the alpha-amylase inhibitor, alpha-glucosidase inhibitor, and dipeptidyl peptidase-IV (DPP-IV) inhibitor. Variations in legume cultivars and methods affect the release of peptides. Different methods have been used, such as in sample preparation, including fermentation (t, T), germination (t), and pre-cooking; in protein extraction, alkaline extraction, isoelectric precipitation, phosphate buffer extraction, and water extraction; in protein hydrolysis enzyme types and combination, enzyme substrate ratio, pH, and time; and in enzyme inhibitory assays, positive control type and concentration, inhibitor or peptide concentration, and the unit of inhibitory activity. The categorization of the relative scale of inhibitory activities among legume samples becomes difficult because of these method differences. Peptide sequences in samples were identified by means of HPLC/MS. Software and online tools were used in bioactivity prediction and computational modelling. The identification of the types and locations of chemical interactions between the inhibitor peptides and enzymes and the type of enzyme inhibition were achieved through computational modelling and enzyme kinetic studies.
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页数:52
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