Purification of peroxidase enzyme from radish species in fast and high yield with affinity chromatography technique

dc.contributor.authorOztekin, A.
dc.contributor.authorAlmaz Z.
dc.contributor.authorGerni S.
dc.contributor.authorErel D.
dc.contributor.authorKocak S.M.
dc.contributor.authorSengül M.E.
dc.contributor.authorOzdemir H.
dc.date.accessioned2020-01-29T18:54:07Z
dc.date.available2020-01-29T18:54:07Z
dc.date.issued2019
dc.departmentFakülteler, Fen-Edebiyat Fakültesi, Moleküler Biyoloji ve Genetik Bölümüen_US
dc.descriptionPubMed ID: 30939412en_US
dc.description.abstractIn this study, an effective single step affinity method is presented for purifying plant peroxidase (POD) enzymes from radish species. This method make possible to purify the enzymes in high yield and purity. Briefly, 10 different 4-amino benzohydrazide derivatives were synthesized and identified as new competitive POD inhibitors. Then, these derivatives were coupled to Sepharose 4B-L-Tyrosine support matrix by diazotization to form the affinity gels. Purification factors were recorded as 54.8% yield - 665-fold, 33.8% yield - 613-fold, 22.7% yield - 595-fold, 34.4% yield - 781-fold, 40.9% yield - 282-fold for turnip (T-POD), black radish (BR-POD), daikon (D-POD), sweet radish (SR-POD) and kohlrabi radish, (KR-POD), respectively. It has also been shown that the affinity gels, which prepared using the 4-amino 3-bromo benzohydrazide and 4-amino 2-nitro benzohydrazide molecules, capable to purify all radish species POD enzymes in high purity and yield. © 2019 Elsevier B.V.en_US
dc.description.sponsorship215Z386en_US
dc.description.sponsorshipThis study was supported by TUBITAK with 215Z386 project number.en_US
dc.identifier.doi10.1016/j.jchromb.2019.03.035
dc.identifier.endpage92en_US
dc.identifier.issn1570-0232
dc.identifier.pmid30939412
dc.identifier.scopus2-s2.0-85063574730
dc.identifier.scopusqualityQ2
dc.identifier.startpage86en_US
dc.identifier.urihttps://dx.doi.org/10.1016/j.jchromb.2019.03.035
dc.identifier.urihttps://hdl.handle.net/20.500.12639/1361
dc.identifier.volume1114-1115en_US
dc.identifier.wosWOS:000465192800010
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherElsevier B.V.en_US
dc.relation.ispartofJournal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciencesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAffinity chromatographyen_US
dc.subjectPeroxidaseen_US
dc.subjectPurificationen_US
dc.subjectRadishen_US
dc.titlePurification of peroxidase enzyme from radish species in fast and high yield with affinity chromatography techniqueen_US
dc.typeArticle

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