Identification of antidiabetic peptides derived from in silico hydrolysis of three ancient grains: Amaranth, Quinoa and Chia

被引:31
作者
Zamudio, Francisco Valenzuela [1 ]
Hidalgo-Figueroa, Sergio Nemorio [2 ]
Andrade, Rolffy Ruben Ortiz [3 ]
Alvarez, Alan Javier Hernandez [4 ]
Campos, Maira Rubi Segura [1 ]
机构
[1] Univ Autonoma Yucatan, Fac Ingn Quim, Perifer Norte Km 33-5,Tablaje Catastral 13615,Colo, Merida 13615, Yucatan, Mexico
[2] Inst Potosino Invest Cient & Tecnol, Camino Presa San Jose 2055,Lomas 4a secc, San Luis Potosi 78216, Mexico
[3] Univ Autonoma Yucatan, Fac Quim, Calle 43 613 x calle 90,Col Inalambrica, Merida 97069, Yucatan, Mexico
[4] Univ Leeds, EC Stoner Bldg Room 8 76a, Leeds LS2 9JT, England
关键词
Bioactive peptides; In silico analysis; Ancient grains; DPP-IV; -Glucosidase; GLUCOSIDASE INHIBITORY PEPTIDES; BIOACTIVE PEPTIDES; SEED PROTEINS; L; BINDING; IV;
D O I
10.1016/j.foodchem.2022.133479
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The antidiabetic potential of bioactive peptides derived from simulated gastrointestinal digestion (SGID) of proteins present in amaranth quinoa and chia was evaluated using their bioactivity profile and theoretical interaction with DPP-IV and alpha-glucosidases. In silico SGID generated 52 different fragments with in vitro anti diabetic activity where fragments PW, PF, PPG, PM, SW, IW, SF, PP, PPL, PG, PY, VW and PL scored highly in bioactivity probability, with molecular weights ranging from 172.2 to 325.44 Da; positive bulkiness index and hydrophobicity (except PP and PY) and no toxic properties. Fragments IW and PW presented the lowest free energy values for enzymes DPP-IV, maltase-glucoamylase, pancreatic alpha-amylase and sucrase-isomaltase (-8.2,-7.5,-7.7 and-7.5 kcal/mol; and-7.8,-7.4,-8.2,-7.4 kcal/mol respectively) We can conclude that proteins from amaranth, quinoa and chia may be a good source of antidiabetic BP and may exert antidiabetic activity through the release of BP after digestion.
引用
收藏
页数:12
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