Synthesis and characterization of pseudo-affinity ligand for penicillin acylase purification


KEÇİLİ R., Say R., Yavuz H.

INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, cilt.39, sa.4-5, ss.250-255, 2006 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 39 Sayı: 4-5
  • Basım Tarihi: 2006
  • Doi Numarası: 10.1016/j.ijbiomac.2006.04.001
  • Dergi Adı: INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.250-255
  • Anahtar Kelimeler: pseudo-affinity ligand, penicillin acylase, methacryloyl antipyrine (MAAP), ESCHERICHIA-COLI, IMMOBILIZATION, CHROMATOGRAPHY, AMIDASE, AID
  • Anadolu Üniversitesi Adresli: Hayır

Özet

The aim of this work was to test a chromatographic affinity support containing methacryloyl antipyrine (MAAP) for penicillin acylase (PA) purification by using pure penicillin acylase and crude extract. First, MAAP as a pseudo-specific ligand was synthesized by using methacryloyl chloride and 4-aminoantipyrine. Polymer beads (average size diameter: 40-120 mu m) were prepared by suspension polymerization of ethylene glycol dimethacrylate (EGDMA) and MAAP. This approach for the preparation of adsorbent has several advantages over conventional preparation protocols. An expensive and time consuming step in the preparation of adsorbent is immobilization of a ligand to the adsorption matrix. In this procedure, affinity ligand MAAP acts as comonomer without further modification steps. Poly(EGDMA-MAAP) beads were characterized by FTIR, NMR and screen analysis. Elemental analysis of MAAP for nitrogen was estimated as 89.3 mu mol/g. The prepared adsorbent was then used for the capture of penicillin acylase in batch system. The maximum penicillin acylase adsorption capacity of the poly(EGDMA-MAAP) beads was found to be 82.2 mg/g at pH 5.0. Chromatography with crude feedstock resulted in 23.2-fold purification and 93% recovery with 1.0 M NaOH. (c) 2006 Elsevier B.V. All rights reserved.