N-methacryloyl-(l)-histidine methyl ester carrying porous magnetic beads for metal chelate adsorption of cytochrome c


AKKAYA B., UZUN L., CANDAN F., DENİZLİ A.

Materials Science and Engineering C, cilt.27, sa.1, ss.180-187, 2007 (SCI-Expanded) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 27 Sayı: 1
  • Basım Tarihi: 2007
  • Doi Numarası: 10.1016/j.msec.2006.04.009
  • Dergi Adı: Materials Science and Engineering C
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.180-187
  • Anahtar Kelimeler: Affinity chromatography, Cytochrome c, Histidine, Magnetic polymers, Metal-chelate affinity beads
  • Hacettepe Üniversitesi Adresli: Evet

Özet

A magnetic metal-chelate adsorbent utilizing N-methacryloyl-(l)-histidine methyl ester (MAH) as a metal-chelating ligand was prepared. MAH was synthesized using methacryloyl chloride and l-histidine methyl ester. Magnetic beads with an average diameter of 50-100 μm were produced by suspension polymerization of ethylene glycol dimethacrylate (EGDMA) and MAH carried out in a dispersion medium. Specific surface area of the magnetic beads was found to be 80 m2/g. Elemental analysis of the magnetic beads for nitrogen was estimated as 70 μmol MAH/g polymer. Magnetic beads were complexed with the Cu2+ ions directly via MAH for the adsorption of cytochrome c from aqueous solutions. The cytochrome c adsorption on the mag-poly(EGDMA-MAH) beads was 51 mg/g. Cu2+ complexing increased the cytochrome c adsorption significantly. The maximum cytochrome c adsorption capacity of the Cu2+-chelated beads (carrying 68 μmol Cu2+ per gram of polymer) was found to be 222 mg/g at pH 8.0 in phosphate buffer. Cytochrome c adsorption decreased with increasing temperature. Cytochrome c molecules could be reversibly adsorbed and desorbed ten times with the magnetic adsorbents without noticeable loss in their cytochrome c adsorption capacity. The resulting magnetic chelator beads posses excellent long term storage stability. © 2006 Elsevier B.V. All rights reserved.