Investigation into IgG/IgE binding capacity and gut microbiota of digestion products derived from glycated ovalbumin

Gut microbiota plays an important role in food allergy. The immunoglobulin G (IgG)/immunoglobulin E (IgE) binding capacity and human gut microbiota changes of digestion products derived from glycated ovalbumin (OVA) were investigated. Gastrointestinal digestion effectively destroyed the primary stru...

Full description

Saved in:
Bibliographic Details
Main Authors: Jihua Mao, Yanhong Shao, Hui Wang, Jun Liu, Zongcai Tu
Format: Article
Language:English
Published: Tsinghua University Press 2024-11-01
Series:Food Science and Human Wellness
Subjects:
Online Access:https://www.sciopen.com/article/10.26599/FSHW.2023.9250045
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1841550145267695616
author Jihua Mao
Yanhong Shao
Hui Wang
Jun Liu
Zongcai Tu
author_facet Jihua Mao
Yanhong Shao
Hui Wang
Jun Liu
Zongcai Tu
author_sort Jihua Mao
collection DOAJ
description Gut microbiota plays an important role in food allergy. The immunoglobulin G (IgG)/immunoglobulin E (IgE) binding capacity and human gut microbiota changes of digestion products derived from glycated ovalbumin (OVA) were investigated. Gastrointestinal digestion effectively destroyed the primary structure of glycated OVA, resulting in a significantly higher digestibility than gastric digestion, and more abundant peptides < 3 kDa. Moreover, gastric and gastrointestinal digestion products have different fluorescence quenching and red shift of fluorescence peaks, and possess different conformational structures. These changes resulted in a decrease in 28.7% of the IgE binding capacity of gastrointestinal digestion products beyond that of pepsin. Moreover, gastrointestinal digestion products of glycated OVA increased significantly the proportion of Subdoligranulum, Collinsella, and Bifidobacterium. Therefore, gastrointestinal digestion products of glycated OVA altered human intestinal microbiota, reducing the risk of potential allergy.
format Article
id doaj-art-e32555843b2b48aa92147b4969235245
institution Kabale University
issn 2097-0765
2213-4530
language English
publishDate 2024-11-01
publisher Tsinghua University Press
record_format Article
series Food Science and Human Wellness
spelling doaj-art-e32555843b2b48aa92147b49692352452025-01-10T06:57:02ZengTsinghua University PressFood Science and Human Wellness2097-07652213-45302024-11-011363633364110.26599/FSHW.2023.9250045Investigation into IgG/IgE binding capacity and gut microbiota of digestion products derived from glycated ovalbuminJihua Mao0Yanhong Shao1Hui Wang2Jun Liu3Zongcai Tu4National R&D Center for Freshwater Fish Processing, College of Life Science, College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, ChinaNational R&D Center for Freshwater Fish Processing, College of Life Science, College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, ChinaState Key Laboratory of Food Science and Technology, Nanchang University, Nanchang 330047, ChinaNational R&D Center for Freshwater Fish Processing, College of Life Science, College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, ChinaNational R&D Center for Freshwater Fish Processing, College of Life Science, College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, ChinaGut microbiota plays an important role in food allergy. The immunoglobulin G (IgG)/immunoglobulin E (IgE) binding capacity and human gut microbiota changes of digestion products derived from glycated ovalbumin (OVA) were investigated. Gastrointestinal digestion effectively destroyed the primary structure of glycated OVA, resulting in a significantly higher digestibility than gastric digestion, and more abundant peptides < 3 kDa. Moreover, gastric and gastrointestinal digestion products have different fluorescence quenching and red shift of fluorescence peaks, and possess different conformational structures. These changes resulted in a decrease in 28.7% of the IgE binding capacity of gastrointestinal digestion products beyond that of pepsin. Moreover, gastrointestinal digestion products of glycated OVA increased significantly the proportion of Subdoligranulum, Collinsella, and Bifidobacterium. Therefore, gastrointestinal digestion products of glycated OVA altered human intestinal microbiota, reducing the risk of potential allergy.https://www.sciopen.com/article/10.26599/FSHW.2023.9250045ovalbuminglycationdigestionigg/ige binding capacitygut microbiota
spellingShingle Jihua Mao
Yanhong Shao
Hui Wang
Jun Liu
Zongcai Tu
Investigation into IgG/IgE binding capacity and gut microbiota of digestion products derived from glycated ovalbumin
Food Science and Human Wellness
ovalbumin
glycation
digestion
igg/ige binding capacity
gut microbiota
title Investigation into IgG/IgE binding capacity and gut microbiota of digestion products derived from glycated ovalbumin
title_full Investigation into IgG/IgE binding capacity and gut microbiota of digestion products derived from glycated ovalbumin
title_fullStr Investigation into IgG/IgE binding capacity and gut microbiota of digestion products derived from glycated ovalbumin
title_full_unstemmed Investigation into IgG/IgE binding capacity and gut microbiota of digestion products derived from glycated ovalbumin
title_short Investigation into IgG/IgE binding capacity and gut microbiota of digestion products derived from glycated ovalbumin
title_sort investigation into igg ige binding capacity and gut microbiota of digestion products derived from glycated ovalbumin
topic ovalbumin
glycation
digestion
igg/ige binding capacity
gut microbiota
url https://www.sciopen.com/article/10.26599/FSHW.2023.9250045
work_keys_str_mv AT jihuamao investigationintoiggigebindingcapacityandgutmicrobiotaofdigestionproductsderivedfromglycatedovalbumin
AT yanhongshao investigationintoiggigebindingcapacityandgutmicrobiotaofdigestionproductsderivedfromglycatedovalbumin
AT huiwang investigationintoiggigebindingcapacityandgutmicrobiotaofdigestionproductsderivedfromglycatedovalbumin
AT junliu investigationintoiggigebindingcapacityandgutmicrobiotaofdigestionproductsderivedfromglycatedovalbumin
AT zongcaitu investigationintoiggigebindingcapacityandgutmicrobiotaofdigestionproductsderivedfromglycatedovalbumin