Dye affinity cryogels for plasmid DNA purification
dc.authorid | 0000-0002-9453-4462 | |
dc.authorid | 0000-0003-0161-172X | |
dc.authorid | 0000-0003-3260-1639 | |
dc.contributor.author | Çimen, Duygu | |
dc.contributor.author | Yılmaz, Fatma | |
dc.contributor.author | Perçin, Işık | |
dc.contributor.author | Türkmen, Deniz | |
dc.contributor.author | Denizli, Adil | |
dc.date.accessioned | 2024-09-25T19:59:47Z | |
dc.date.available | 2024-09-25T19:59:47Z | |
dc.date.issued | 2015 | |
dc.department | BAİBÜ, Gerede Meslek Yüksekokulu, Kimya Ve Kimyasal İşleme Teknolojileri Bölümü | en_US |
dc.description.abstract | The aim of this study is to prepare megaporous dye-affinity cryogel discs for the purification of plasmid DNA (pDNA) from bacterial lysate. Poly(hydroxyethyl methacrylate) [PHEMA] cryogel discs were produced by free radical polymerization initiated by N,N,N',N'-tetramethylene diamine (TEMED) and ammonium persulfate (APS) redox pair in an ice bath. Cibacron Blue F3GA was used as an affinity ligand (loading amount: 68.9 mu mol/g polymer). The amount of pDNA adsorbed onto the PHEMA-Cibacron Blue F3GA cryogel discs first increased and then reached a plateau value (i.e., 32.5 mg/g cryogel) at 3.0 mg/mL pDNA concentration. Compared with the PHEMA cryogel (0.11 mg/g cryogel), the pDNA adsorption capacity of the PHEMA-Cibacron Blue F3GA cryogel (32.4 mg/g polymer) was improved significantly due to the Cibacron Blue 3GA immobilization onto the polymeric matrix. pDNA adsorption amount decreased from 11.7 mg/g to 1.1 mg/g with the increasing of NaCl concentration. The maximum pDNA adsorption was achieved at 4 degrees C The overall recovery of pDNA was calculated as 90%. The PHEMA-Cibacron Blue F3GA cryogel discs could be used five times without decreasing the pDNA adsorption capacity significantly. The results show that the PHEMA-Cibacron Blue F3GA cryogel discs promise high selectivity for pDNA. (C) 2015 Elsevier B.V. All rights reserved. | en_US |
dc.identifier.doi | 10.1016/j.msec.2015.06.041 | |
dc.identifier.endpage | 324 | en_US |
dc.identifier.issn | 0928-4931 | |
dc.identifier.issn | 1873-0191 | |
dc.identifier.pmid | 26249596 | en_US |
dc.identifier.startpage | 318 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.msec.2015.06.041 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12491/13912 | |
dc.identifier.volume | 56 | en_US |
dc.identifier.wos | WOS:000359873900038 | en_US |
dc.identifier.wosquality | Q2 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.institutionauthor | Yılmaz, Fatma | |
dc.institutionauthorid | 0000-0003-3260-1639 | |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.ispartof | Materials Science & Engineering C-Materials For Biological Applications | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.snmz | YK_20240925 | en_US |
dc.subject | PHEMA | en_US |
dc.subject | Cryogels | en_US |
dc.subject | Cibacron Blue F3GA | en_US |
dc.subject | DNA purification | en_US |
dc.subject | Affinity adsorption | en_US |
dc.title | Dye affinity cryogels for plasmid DNA purification | en_US |
dc.type | Article | en_US |
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