Characterization and Modification of Antioxidant Proteins From Plat Materials

dc.contributor.advisor Yemenicioğlu, Ahmet
dc.contributor.author Arcan, İskender
dc.date.accessioned 2014-07-22T13:51:09Z
dc.date.available 2014-07-22T13:51:09Z
dc.date.issued 2005
dc.description Thesis (Master)--İzmir Institute of Technology, Biotechnology and Bioengineering, İzmir, 2005 en_US
dc.description Includes bibliographical references (leaves: 73-75) en_US
dc.description Text in English; Abstract: Turkish and English en_US
dc.description xiv, 92 leaves en_US
dc.description.abstract In this study, the radical scavenging and iron chelating capacity of proteins from heat treated (20 min at 90 oC) or thermally processed (20 min at 121 oC) chick-peas andkidney-beans were compared. Lyophilized crude protein extracts from chick-peas contained more protein (1.5-3 fold) and showed higher free radical scavenging (up to 2.3 fold) and iron binding capacity (up to 3 fold) than lyophilized crude protein extracts form kidney-beans. The thermal processing of chick-peas did not cause a significant change in the radical scavenging capacity of their lyophilized crude protein extracts, but improved the iron chelating capacity of these proteins almost 80 %. However, the thermal processing reduced both the radical scavenging and iron binding capacity of crude lyophilized proteins form kidney beans by 20-40 % and 60 %, respectively.Partial purification by ammonium sulfate precipitation or DEAE-cellulose chromatography increased the antioxidant capacity of thermally processed chick-pea proteins. The DEAE cellulose chromatography also showed the presence of 5 and 3 antioxidant protein fractions in heat treated and thermally processed chick-peas, respectively. Hot acidic hydrolysis at 80 oC for 30 min in presence of 1.5 M HCl increases the specific antioxidant activity of protein extracts, but causes the formation of undesired Maillard reaction products. Hot extraction at 85 oC for 30 min at pH 2.5 extracts the antioxidant proteins selectively, whereas 85 oC for 30 min at pH 9.5 extracts both antioxidant proteins and other proteins. en_US
dc.identifier.uri https://hdl.handle.net/11147/3234
dc.language.iso en en_US
dc.publisher Izmir Institute of Technology en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject.lcsh Proteins en
dc.subject.lcsh Proteins--Purification en
dc.subject.lcsh Antioxidants en
dc.title Characterization and Modification of Antioxidant Proteins From Plat Materials en_US
dc.type Master Thesis en_US
dspace.entity.type Publication
gdc.author.institutional Arcan, İskender
gdc.coar.access open access
gdc.coar.type text::thesis::master thesis
gdc.description.department Thesis (Master)--İzmir Institute of Technology, Bioengineering en_US
gdc.description.publicationcategory Tez en_US
gdc.description.scopusquality N/A
gdc.description.wosquality N/A
relation.isAuthorOfPublication.latestForDiscovery eb89c462-e09e-444b-b60a-7226340831a0
relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4019-8abe-a4dfe192da5e

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