Optimisation and Characterisation of the Protein Hydrolysate of Scallops (Argopecten purpuratus) Visceral By-Products

In this research, scallops (Argopecten purpuratus) visceral meal (SVM) and defatted meal (SVMD) were analysed for their proximal composition, protein solubility, and amino acid profile. Hydrolysed proteins isolated from the scallop’s viscera (SPH) were optimised and characterised using response surf...

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Bibliographic Details
Authors: Chasquibol Silva, Nancy Ascención, Gonzales Garcia, Billy Francisco, Alarcón Rivera, Rafael, Sotelo Contreras, Axel, Márquez-López, José Carlos, Rodríguez-Martin, Noelia M., Millán-Linares, María del Carmen, Millán, Francisco, Pedroche, Justo
Format: article
Publication Date:2023
Country:Perú
Institution:Universidad de Lima
Repository:ULIMA-Institucional
Language:English
OAI Identifier:oai:repositorio.ulima.edu.pe:20.500.12724/18333
Online Access:https://hdl.handle.net/20.500.12724/18333
https://doi.org/10.3390/foods12102003
Access Level:Open access
Keyword:Proteins
Amino acids
Enzymes
Proteínas
Aminoácidos
Enzimas
https://purl.org/pe-repo/ocde/ford#2.11.04
Description
Summary:In this research, scallops (Argopecten purpuratus) visceral meal (SVM) and defatted meal (SVMD) were analysed for their proximal composition, protein solubility, and amino acid profile. Hydrolysed proteins isolated from the scallop’s viscera (SPH) were optimised and characterised using response surface methodology with a Box-Behnken design. The effects of three independent variables were examined: temperature (30–70 °C), time (40–80 min), and enzyme concentration (0.1–0.5 AU/g protein) on the degree of hydrolysis (DH %) as a response variable. The optimised protein hydrolysates were analysed for their proximal composition, yield, DH %, protein solubility, amino acid composition, and molecular profile. This research showed that defatted and isolation protein stages are not necessaries to obtain the hydrolysate protein. The conditions of the optimization process were 57 °C, 62 min and 0.38 AU/g protein. The amino acid composition showed a balanced profile since it conforms to the Food and Agriculture Organisation/World Health Organisation recommendations for healthy nutrition. The predominant amino acids were aspartic acid + asparagine, glutamic acid + Glutamate, Glycine, and Arginine. The protein hydrolysates’ yield and DH % were higher than 90% and close to 20%, respectively, with molecular weight between 1–5 kDa. The results indicate that the protein hydrolysates of scallops (Argopecten purpuratus) visceral by product optimised and characterised was suitable a lab-scale. Further research is necessary to study the bioactivity properties with biologic activity of these hydrolysates.