Article

Characterization of Yeast Protein Hydrolysate for Potential Application as a feed additive

Ju Hyun Min1, Yeon Ju Lee1, Hye Jee Kang1, Na Rae Moon1, Young Kook Park2, Seon Tae Joo3, Young Hoon Jung1,*
Author Information & Copyright
1School of Food Science and Biotechnology, Kyungpook National University, Daegu 41566, Korea.
2Amored Fresh of Food Tech Co, Seoul 06693, Korea.
3Division of Applied Life Science (BK21 Four), Institute of Agriculture & Life Science, Gyeongsang National University, Jinju 52852, Korea.
*Corresponding Author: Young Hoon Jung. E-mail: younghoonjung@knu.ac.kr.

© Copyright 2024 Korean Society for Food Science of Animal Resources. This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Received: Mar 25, 2024 ; Revised: Apr 12, 2024 ; Accepted: Apr 15, 2024

Published Online: Apr 19, 2024

Abstract

Yeast protein can be a nutritionally suitable auxiliary protein source in livestock food. The breakdown of proteins and thereby generating high-quality peptides, typically provides nutritional benefits. enzyme hydrolysis has been effectively used; however, studies on the potential applications of different types of enzymes to produce yeast protein hydrolysates remain limited. This study investigated the effects of endo- (alcalase and neutrase) and exotype (flavourzyme and prozyme 2000P) enzyme treatments on yeast protein during the production of enzymatic protein hydrolysates. Endotype enzymes facilitate a higher hydrolysis efficiency in yeast proteins than exotype enzymes. The highest degree of hydrolysis was observed for the protein treated with neutrase, which was followed by alcalase, prozyme 2000P, and flavourzyme.  Furthermore, endotype enzyme treated proteins exhibited higher solubility than their exotype counterparts. Notably, the more uniform particle size distribution was observed in endotype treated yeast protein. Moreover, compared with the original yeast protein, the enzymatic protein hydrolysates possessed a higher content of β-sheets and random coil structures, indicating their higher structural stability. Regardless of enzyme type, enzyme treated protein possessed a higher total free amino acid content including essential amino acids. Therefore, this study provides significant insights into the production of enzymatic protein hydrolysates as an alternative protein material.

Keywords: yeast protein; endoprotease; exoprotease; hydrolysis; alternative protein