Tentacle-type immobilized metal affinity cryogel for invertase purification from Saccharomyces cerevisiae


ÇETİN K., PERÇİN DEMİRÇELİK I., Denizli F., DENİZLİ A.

ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY, cilt.45, sa.7, ss.1431-1439, 2017 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 45 Sayı: 7
  • Basım Tarihi: 2017
  • Doi Numarası: 10.1080/21691401.2016.1243549
  • Dergi Adı: ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1431-1439
  • Anahtar Kelimeler: PEI, coordinate binding, cryogel, IMAC, invertase, Saccharomyces cerevisiae, YEAST INVERTASE, ION AFFINITY, HUMAN PLASMA, LIQUID-CHROMATOGRAPHY, IMPRINTED CRYOGELS, IMMUNOGLOBULIN-G, PROTEIN-BINDING, CHELATED BEADS, ACID INVERTASE, HUMAN SERUM
  • Hacettepe Üniversitesi Adresli: Evet

Özet

The aim of this study is to investigate the usability of cryogel columns for the purification of invertase from Saccharomyces cerevisiae. Poly(2-hydroxyethyl methacrylate) monolithic columns were produced via cryogelation. Ester groups of the poly(2-hydroxyethyl methacrylate) structure were then converted to imine groups by the reaction with poly(ethylene imine) in the presence of NaHCO3. Transition metal ions, Cu(II), Co(II), and Ni(II), were chelated on the PEI-modified cryogel columns. Purification of invertase from natural source namely S. cerevisiae was also studied, and the purification fold values were obtained as 41.350, 44.714, and 30.302 for Cu(II)-chelated, Co(II)-chelated, and Ni(II)-chelated PHEMA/PEI columns, respectively.