Isolation and characterisation of milk-derived amyloid-like protein aggregates (MAPA) from cottage cheese

被引:6
|
作者
Malik, Shweta [1 ]
De, Indranil [2 ]
Singh, Manish [2 ]
Galanakis, Charis M. [3 ,4 ,5 ]
Alamri, Abdulhakeem S. [5 ,6 ]
Yadav, Jay Kant [1 ]
机构
[1] Cent Univ Rajasthan, Sch Life Sci, Dept Biotechnol, NH 8 Bandarsindri, Ajmer 305817, Rajasthan, India
[2] Inst Nano Sci & Technol, Mohali 160062, Punjab, India
[3] Galanakis Labs, Res & Innovat Dept, Khania, Greece
[4] ISEKI Food Assoc, Food Waste Recovery Grp, Vienna, Austria
[5] Taif Univ, Coll Appl Med Sci, Dept Clin Lab Sci, At Taif, Saudi Arabia
[6] Taif Univ, Ctr Biomed Sci Res CBSR, Deanship Sci Res, At Taif, Saudi Arabia
关键词
Amyloids; Bovine milk caseins; Cottage cheese; Protein aggregation; FIBRIL FORMATION; CASEIN; BETA; IDENTIFICATION; FLUORESCENCE; PREDICTION; PEPTIDES; HEAT; WHEY;
D O I
10.1016/j.foodchem.2021.131486
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Cottage cheese, extensively consumed worldwide, contains coagulated milk protein (casein), produced through boiling and acidification of milk. Casein forms amyloid or amyloid-like structures at high temperatures and low pH. Due to the similarities in the preparation of casein amyloids and cottage cheese, we hypothesized the presence of amyloid or amyloid-like protein aggregates in cottage cheese. To examine this hypothesis, cottage cheese was prepared from cow (Bos indicus) milk and isolated amyloids through a water extraction method. The isolated protein aggregates displayed typical characteristics of amyloids, such as a bathochromic shift in the wavelength of maximum absorption (lambda max) of Congo red (CR), high thioflavin T (ThT) binding, increased surface hydrophobicity, and high B-sheet structure. However, they did not show antibacterial activity and toxic properties against erythrocytes. Our study revealed that the heat-treatment and subsequent acidification during cottage cheese preparation lead to the formation of non-toxic amyloid-like aggregates.
引用
收藏
页数:10
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