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Optimization of hydrolysis conditions for bovine plasma protein using response surface methodology

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dc.contributor.authorSeo, Hyun-Woo-
dc.contributor.authorJung, Eun-Young-
dc.contributor.authorGo, Gwang-woong-
dc.contributor.authorKim, Gap-Don-
dc.contributor.authorJoo, Seon-Tea-
dc.contributor.authorYang, Han-Sul-
dc.date.accessioned2022-12-26T21:31:20Z-
dc.date.available2022-12-26T21:31:20Z-
dc.date.issued2015-10-15-
dc.identifier.issn0308-8146-
dc.identifier.issn1873-7072-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/16963-
dc.description.abstractThe purpose of this study was to establish optimal conditions for the hydrolysis of bovine plasma protein. Response surface methodology was used to model and optimize responses [degree of hydrolysis (DH), 2,2-diphenyl-1-picrydrazyl (DPPH) radical-scavenging activity and Fe2+-chelating activity]. Hydrolysis conditions, such as hydrolysis temperature (46.6-63.4 degrees C), hydrolysis time (98-502 min), and hydrolysis pH (6.32-9.68) were selected as the main processing conditions in the hydrolysis of bovine plasma protein. Optimal conditions for maximum DH (%), DPPH radical-scavenging activity (%) and Fe2+-chelating activity (%) of the hydrolyzed bovine plasma protein, were respectively established. We discovered the following three conditions for optimal hydrolysis of bovine plasma: pH of 7.82-8.32, temperature of 54.1 degrees C, and time of 338.4-398.4 min. We consequently succeeded in hydrolyzing bovine plasma protein under these conditions and confirmed the various desirable properties of optimal hydrolysis. (C) 2015 Elsevier Ltd. All rights reserved.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCI LTD-
dc.titleOptimization of hydrolysis conditions for bovine plasma protein using response surface methodology-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.foodchem.2015.03.133-
dc.identifier.scopusid2-s2.0-84926472097-
dc.identifier.wosid000355027100014-
dc.identifier.bibliographicCitationFOOD CHEMISTRY, v.185, pp 106 - 111-
dc.citation.titleFOOD CHEMISTRY-
dc.citation.volume185-
dc.citation.startPage106-
dc.citation.endPage111-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaFood Science & Technology-
dc.relation.journalResearchAreaNutrition & Dietetics-
dc.relation.journalWebOfScienceCategoryChemistry, Applied-
dc.relation.journalWebOfScienceCategoryFood Science & Technology-
dc.relation.journalWebOfScienceCategoryNutrition & Dietetics-
dc.subject.keywordPlusRADICAL SCAVENGING ACTIVITY-
dc.subject.keywordPlusANTIOXIDANT ACTIVITY-
dc.subject.keywordPlusFUNCTIONAL-PROPERTIES-
dc.subject.keywordPlusPEPTIDES-
dc.subject.keywordPlusEXTRACT-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordPlusBLOOD-
dc.subject.keywordAuthorResponse surface methodology-
dc.subject.keywordAuthorOptimization-
dc.subject.keywordAuthorPlasma protein hydrolysates-
dc.subject.keywordAuthorDPPH radical scavenging activity-
dc.subject.keywordAuthorFe2+ chelating activity-
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