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A new approach for affinity-based purification of horseradish peroxidase.

Zuleyha AlmazAykut ÖztekinNurgul AbulSerpil GerniDeniz ErelSeyma Mehtap KocakMehmet Emin SengülHasan Ozdemir
Published in: Biotechnology and applied biochemistry (2020)
We have developed efficient procedure for isolation of horseradish peroxidase (HRP) using aminobenzohydrazide-based affinity chromatography. Sepharose 4B-bounded aminobenzohydrazides are suitable for long-term use and large-scale purification. In this study, 26 aminobenzohydrazide derivatives were synthesized, characterized and defined as new HRP inhibitors. In addition, detailed inhibition effects of these molecules on HRP enzyme were investigated. Affinity matrix was formed by bonding aminobenzohydrazides, which exhibited inhibitory activity to sepharose-4B-l-tyrosine. HRP was isolated from crude homogenate in single step and purification factors were recorded as 1,151-fold (recovery of 8.5%) with 4-amino 3-bromo benzohydrazide and as 166.16-fold (recovery of 16.67 %) with 3-amino 4-chloro benzohydrazide.
Keyphrases
  • hydrogen peroxide
  • capillary electrophoresis
  • mass spectrometry
  • recombinant human
  • high speed
  • minimally invasive
  • atomic force microscopy
  • nitric oxide
  • high resolution