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Evaluation of intermediate compounds in β-carboline alkaloids formation using model system including isotope labeled glycerol
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Lim, Kyung-Jik | - |
| dc.contributor.author | Shin, Han-Seung | - |
| dc.date.accessioned | 2025-08-05T03:00:12Z | - |
| dc.date.available | 2025-08-05T03:00:12Z | - |
| dc.date.issued | 2025-11 | - |
| dc.identifier.issn | 0308-8146 | - |
| dc.identifier.issn | 1873-7072 | - |
| dc.identifier.uri | https://scholarworks.dongguk.edu/handle/sw.dongguk/58863 | - |
| dc.description.abstract | β-carbolines (βCs) such as norharman and harman are thermally formed in foods and have been associated with neurotoxic and mutagenic effects. This study explores glycerol-derived intermediates in βC formation, identifying 3-vinylindole as a key intermediate via isotope labeling. Model systems with labeled glycerol were used for carbon tracing. Quantitation and structural analysis were performed by HPLC, LC-MS/MS, and ESI-qTOF-MS/MS. In applied model system, formaldehyde levels increased from 33.77 to 77.12 mg/kg. Correspondingly, norharman concentrations rose from 98.59 to 680.19 μg/kg, demonstrating a dose-dependent relationship between glycerol content and βC formation. Time-resolved profiling showed 3-vinylindole peaked at 10 min and declined, while norharman concentration concurrently increased, supporting its role as a transient intermediate. Isotope tracing further confirmed a + 2 Da mass shift in 3-vinylindole, indicating the incorporation of glycerol-derived carbons. These findings elucidate a novel pathway for βC formation under thermal conditions and highlight glycerol's contribution to this process during food processing. © 2025 Elsevier Ltd | - |
| dc.format.extent | 11 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | Elsevier Ltd | - |
| dc.title | Evaluation of intermediate compounds in β-carboline alkaloids formation using model system including isotope labeled glycerol | - |
| dc.type | Article | - |
| dc.publisher.location | 네델란드 | - |
| dc.identifier.doi | 10.1016/j.foodchem.2025.145522 | - |
| dc.identifier.scopusid | 2-s2.0-105011032830 | - |
| dc.identifier.wosid | 001541382800002 | - |
| dc.identifier.bibliographicCitation | Food Chemistry, v.492, pp 1 - 11 | - |
| dc.citation.title | Food Chemistry | - |
| dc.citation.volume | 492 | - |
| dc.citation.startPage | 1 | - |
| dc.citation.endPage | 11 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalResearchArea | Food Science & Technology | - |
| dc.relation.journalResearchArea | Nutrition & Dietetics | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Applied | - |
| dc.relation.journalWebOfScienceCategory | Food Science & Technology | - |
| dc.relation.journalWebOfScienceCategory | Nutrition & Dietetics | - |
| dc.subject.keywordPlus | PICTET-SPENGLER REACTION | - |
| dc.subject.keywordPlus | HETEROCYCLIC AMINES | - |
| dc.subject.keywordPlus | MASS-SPECTROMETRY | - |
| dc.subject.keywordPlus | MAILLARD REACTION | - |
| dc.subject.keywordPlus | IDENTIFICATION | - |
| dc.subject.keywordPlus | TRYPTOPHAN | - |
| dc.subject.keywordAuthor | Aldehydes | - |
| dc.subject.keywordAuthor | Glycerol | - |
| dc.subject.keywordAuthor | Indole-based intermediate | - |
| dc.subject.keywordAuthor | Thermal reaction | - |
| dc.subject.keywordAuthor | β-Carboline alkaloid | - |
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