Effect of thermal treatment on secondary structure and conformational change of mushroom polyphenol oxidase (PPO) as food quality related enzyme: A FTIR study

Baltacioglu H., Bayındırlı A., Severcan M., Severcan F.

FOOD CHEMISTRY, cilt.187, ss.263-269, 2015 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 187
  • Basım Tarihi: 2015
  • Doi Numarası: 10.1016/j.foodchem.2015.04.097
  • Dergi Adı: FOOD CHEMISTRY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.263-269
  • Anahtar Kelimeler: PPO, Heat inactivation, FTIR, Spectroscopy, Protein secondary structure, TRANSFORM INFRARED-SPECTROSCOPY, AGARICUS-BISPORUS, IR SPECTROSCOPY, RAT-BRAIN, INACTIVATION, PRESSURE, INFORMATION, TYROSINASE, SPECTRA, THERMODYNAMICS
  • Orta Doğu Teknik Üniversitesi Adresli: Evet

Özet

In order to understand the conformational changes of polyphenol oxidase (PPO), which is a food quality related enzyme, after thermal treatment, secondary structure changes of the enzyme were analyzed by using Fourier Transform Infrared (FTIR) spectroscopy and compared with the change in enzyme activity in the temperature range of 25-80 degrees C. Fourier self-deconvolution, neural network (NN) and curve-fitting analysis were applied to the amide I band of FTIR spectra for detail analysis of secondary structure elements. FTIR analysis indicated that PPO is an a-helix dominating enzyme. Detail analysis revealed that, as temperature increased, alpha-helix and beta-sheet decreased, but aggregated beta-sheet, turns and random coil increased. The marked changes were noted at 40 degrees C with the occurrence of new bands due to aggregated beta-sheet structures, all of which indicate protein denaturation. These aggregation bands were still observed when the temperature was reduced back to 25 degrees C, from 70 degrees C, demonstrating an irreversible change in the structure. (C) 2015 Elsevier Ltd. All rights reserved.