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Publication:
Effect of Thermal Treatment on Secondary Structure and Conformational Change of Mushroom Polyphenol Oxidase (PPO) as Food Quality Related Enzyme: A FTIR Study

dc.authorscopusid56606296900
dc.authorscopusid6601954584
dc.authorscopusid56027352100
dc.authorscopusid7004161587
dc.contributor.authorBaltacioʇlu, H.
dc.contributor.authorBayindirli, A.
dc.contributor.authorSevercan, M.
dc.contributor.authorSevercan, F.
dc.date.accessioned2020-06-21T13:41:38Z
dc.date.available2020-06-21T13:41:38Z
dc.date.issued2015
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Baltacioʇlu] Hande, Department of Food Engineering, Middle East Technical University (METU), Ankara, Ankara, Turkey, Department of Food Engineering, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Bayindirli] Alev, Department of Food Engineering, Middle East Technical University (METU), Ankara, Ankara, Turkey; [Severcan] Mete, Department of Electrical and Electronic Engineering, Middle East Technical University (METU), Ankara, Ankara, Turkey; [Severcan] Feride, Department of Biological Sciences, Middle East Technical University (METU), Ankara, Ankara, Turkeyen_US
dc.description.abstractIn order to understand the conformational changes of polyphenol oxidase (PPO), which is a food quality related enzyme, after thermal treatment, secondary structure changes of the enzyme were analyzed by using Fourier Transform Infrared (FTIR) spectroscopy and compared with the change in enzyme activity in the temperature range of 25-80 °C. Fourier self-deconvolution, neural network (NN) and curve-fitting analysis were applied to the amide I band of FTIR spectra for detail analysis of secondary structure elements. FTIR analysis indicated that PPO is an α-helix dominating enzyme. Detail analysis revealed that, as temperature increased, α-helix and β-sheet decreased, but aggregated β-sheet, turns and random coil increased. The marked changes were noted at 40 °C with the occurrence of new bands due to aggregated β-sheet structures, all of which indicate protein denaturation. These aggregation bands were still observed when the temperature was reduced back to 25 °C, from 70 °C, demonstrating an irreversible change in the structure. © 2015 Elsevier Ltd. All rights reserved.en_US
dc.identifier.doi10.1016/j.foodchem.2015.04.097
dc.identifier.endpage269en_US
dc.identifier.isbn9783540699330
dc.identifier.isbn9781619421257
dc.identifier.issn0308-8146
dc.identifier.issn1873-7072
dc.identifier.pmid25977025
dc.identifier.scopus2-s2.0-84928493730
dc.identifier.scopusqualityQ1
dc.identifier.startpage263en_US
dc.identifier.urihttps://doi.org/10.1016/j.foodchem.2015.04.097
dc.identifier.volume187en_US
dc.identifier.wosWOS:000355885400036
dc.identifier.wosqualityQ1
dc.language.isoenen_US
dc.publisherElsevier Ltden_US
dc.relation.ispartofFood Chemistryen_US
dc.relation.journalFood Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectFTIRen_US
dc.subjectHeat Inactivationen_US
dc.subjectPPOen_US
dc.subjectProtein Secondary Structureen_US
dc.subjectSpectroscopyen_US
dc.titleEffect of Thermal Treatment on Secondary Structure and Conformational Change of Mushroom Polyphenol Oxidase (PPO) as Food Quality Related Enzyme: A FTIR Studyen_US
dc.typeArticleen_US
dspace.entity.typePublication

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