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Persistent Identifier
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perma:LIST.N8XQVL |
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Publication Date
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2026-07-06 |
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Title
| Identification of amadori products and oligosaccharide-glycated amino acids in brewer’s spent grain extract [* Cross-Reference *] |
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Other Identifier
| https://doi.org/10.3389/frfst.2022.968865
OpenAlex ID: https://openalex.org/W4293660831 |
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Author
| Martina Minestrini (Luxembourg Institute of Science and Technology)
Sophie Charton (Luxembourg Institute of Science and Technology)Luxembourg Institute of Science and TechnologyORCIDhttps://orcid.org/0000-0002-7941-4657
Marcus Iken (INTRASOFT International (Luxembourg))
Yvan Larondelle (UCLouvain)UCLouvainORCIDhttps://orcid.org/0000-0001-7770-6747
Jenny Renaut (Luxembourg Institute of Science and Technology)Luxembourg Institute of Science and TechnologyORCIDhttps://orcid.org/0000-0002-0450-3866
Jean-François Hausman (Luxembourg Institute of Science and Technology)Luxembourg Institute of Science and TechnologyORCIDhttps://orcid.org/0000-0001-6103-7817
Kjell Sergeant (Luxembourg Institute of Science and Technology)Luxembourg Institute of Science and TechnologyORCIDhttps://orcid.org/0000-0003-2071-3510 |
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Point of Contact
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Use email button above to contact.
LIST QDKM (LIST) |
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Description
| Brewer’s spent grain (BSG) is the most abundant by-product of the brewery industry. Its accessibility and chemical composition allow this material to be recycled for new applications mainly targeting the food industry, based on the health-promoting properties of phenolics in BSG extracts. This study investigates the major compounds identified in food-grade extracts from BSG by UHPLC-ESI-MS/MS analyses, with a focus on the presence of Amadori products. These fructosyl-derivatives are identified for most of the proteinogenic amino acids but for instance also for gamma-aminobutyric acid. While previously proposed to be formed, we show that Amadori products are formed by reaction of amino acses, with a focus on the presence of Amadori products. These fructosyl-derivatives are identified for most of the proteinogenic amino acids but for instance also for gamma-aminobutyric acid. While previously proposed to be formed, we show that Amadori products are formed by reaction of amino acids with oligosaccharides up to five hexoses. Moreover, the same glycation pattern was also observed for other nitrogen-containing compounds such as phosphatidylethanolamine lipids. The presence of these Maillard reaction products and glycated forms of amino-compounds, due to heat-treatment during brewing or stabilization of BSG prior to further processing, may impact the valorization of this by-product and should thus be considered in future studies. (2022-08-30)
***This entry has been automatically imported via OpenAlex by LIST harvest scripts. Please refer to https://doi.org/10.3389/frfst.2022.968865 for the original and latest version of the publication*** (2026-07-01) |
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Subject
| Agricultural Sciences; Arts and Humanities; Chemistry; Medicine, Health and Life Sciences |
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Keyword
| Amadori rearrangement
Maillard reaction
Chemistry
Glycation
Amino acid
Food industry
Biochemistry
Food science
Organic chemistry |
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Topic Classification
| GABA and Rice Research
Advanced Glycation End Products research
Protein Hydrolysis and Bioactive Peptides |
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Deposit Date
| 2022-08-30 |
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Data Type
| Article |
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Data Source
| Frontiers in Food Science and Technology |