Article

A highly sensitive indirect enzyme-linked immunosorbent assay (ELISA) based on a monoclonal antibody specific to thermal stable-soluble protein of pork fat tissue for the detection of pork fat mixed in heat-processed beef meatballs

Sol-A Kim1, Jeong-Eun Lee2, Dong-Hyun Kim1, Song-min Lee1, Hee-Kyeong Yang1, Won-Bo Shim2,3,4,*
Author Information & Copyright
1Division of Applied Life Science, Graduate School, Gyeongsang National University, Jinju, Gyeongnam 52828, Korea.
2Institute of Smart Farm, Gyeongsang National University, Jinju, Gyeongnam, 52828, Korea
3Division of Food Science and Technology, Gyeongsang National University, Jinju, Gyeongnam 52828, Korea
4Institute of Agriculture and Life Science, Gyeongsang National University, Jinju, Gyeongnam 52828, Korea
*Corresponding Author: Won-Bo Shim. E-mail: wbshim@gnu.ac.kr.

© Copyright 2023 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: Aug 12, 2023 ; Revised: Sep 08, 2023 ; Accepted: Sep 14, 2023

Published Online: Sep 21, 2023

Abstract

Processed foods containing pork fat tissue to improve flavor and gain economic benefit may cause severe issues for Muslims, Jews, and vegetarians. This study aimed to develop an indirect enzyme-linked immunosorbent assay (iELISA) based on a monoclonal antibody specific to thermal stable-soluble protein (TSSP) in pork fat tissue and apply it to detect pork fat tissue in heat-processed (autoclave, steam, roast, and fry) beef meatballs. To develop a sensitive iELISA, the optimal sample pre-cooking time, coating conditions, primary and secondary dilution time, and various buffer systems were tested. The change in the iELISA sensitivity with different 96-well microtiter microplates was confirmed. The detection limit of iELISA performed with an appropriate microplate was 0.015% (w/w) pork fat in raw and heat-treated beef. No cross-reactions to other meats or fats were shown. These results mean that the iELISA can be used as an analytical method to detect trace amounts of pork fat mixed in beef.

Keywords: Pork fat tissue; iELISA; Thermal stable-soluble protein (TSSP); Monoclonal antibody