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Phospholipids molecular species, proteins secondary structure, and emulsion microstructure of egg yolk with reduced polar and/or nonpolar lipids

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dc.contributor.authorRahman, M.S.-
dc.contributor.authorKim, A.-N.-
dc.contributor.authorLee, K.-Y.-
dc.contributor.authorPyo, M.-J.-
dc.contributor.authorChun, J.-
dc.contributor.authorKim, H.-J.-
dc.contributor.authorChoi, S.-G.-
dc.date.accessioned2023-03-24T08:47:14Z-
dc.date.available2023-03-24T08:47:14Z-
dc.date.issued2023-04-
dc.identifier.issn0141-8130-
dc.identifier.issn1879-0003-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/30151-
dc.description.abstractThis study investigated the phospholipids (PLs) molecular species (PLs-MS), protein secondary structure (PSS), and emulsion microstructure of the egg yolk (EY) treated with supercritical-CO2 (T1), hexane (T2), and ethanol {at room temperature (T3) and 65 °C (T4)}. PLs-MS, PSS, and microstructure of EY emulsion were investigated with UPLC-Q-TOF-MS, Fourier-transforms infrared and Raman spectroscopy, and confocal laser scanning microscope, respectively. Predominant PLs molecular fractions were C18:0-C20:4, C18:0-C20:4, C16:0-C18:2, C16:0, C18:0-C18:2, and d18:1/16:0, for phosphatidylcholine, phosphatidylethanolamine, phosphatidylinositol, lysophosphatidylcholine, sphingomyelin, and phosphatidylserine, respectively. All the PLs-MS were highest for T1 and many of them (C14:0-C16:0, C18:0-C18:1, C18:0-C20:3) were absent in T2, T3, and T4. PSS components (α–helices, β–sheets, β-turn, and random coil) were highest for T4, followed by T3, T2, T1, and control (non-treated EY). However, T1-added o/w emulsion showed excellent stability (95.64 %) with smaller and denser oil droplets due to better ionic interactions by synergistic effect of PLs-MS and PSS components. © 2023 Elsevier B.V.-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titlePhospholipids molecular species, proteins secondary structure, and emulsion microstructure of egg yolk with reduced polar and/or nonpolar lipids-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.ijbiomac.2023.123529-
dc.identifier.scopusid2-s2.0-85147704250-
dc.identifier.wosid000964452100001-
dc.identifier.bibliographicCitationInternational Journal of Biological Macromolecules, v.233-
dc.citation.titleInternational Journal of Biological Macromolecules-
dc.citation.volume233-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Applied-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.subject.keywordPlusWHEY-PROTEIN-
dc.subject.keywordPlusRAMAN-SPECTROSCOPY-
dc.subject.keywordPlusCHOLESTEROL-
dc.subject.keywordPlusSOY-
dc.subject.keywordPlusEXTRACTION-
dc.subject.keywordPlusSTABILITY-
dc.subject.keywordPlusSYSTEMS-
dc.subject.keywordAuthorEgg yolk-
dc.subject.keywordAuthorEmulsion microstructure-
dc.subject.keywordAuthorOrganic solvent-
dc.subject.keywordAuthorPhospholipids molecular species-
dc.subject.keywordAuthorPolar/nonpolar lipid-
dc.subject.keywordAuthorProteins secondary structure-
dc.subject.keywordAuthorSupercritical-CO2-
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