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Enzymatic hydrolysis for functionalisation of watermelon seed protein from ultrasound-assisted extraction in comparison to soy protein isolate

  • Ezgi Şenol
  • , Beraat Özçelik
  • , Sybille Neidhart
  • , Martin Leitenberger
  • , Mario Jekle*
  • *Bu çalışma için yazışmadan sorumlu yazar
  • Istanbul Technical University
  • University of Hohenheim

Araştırma çıktısı: Dergi yayını › Makale › Hakemli

5 Atıf (Scopus)

Özet

The functional characteristics of a watermelon seed protein isolate (UA-WSPI), which resulted from an underutilised protein source by ultrasound-assisted extraction and freeze-drying, and a commercial spray-dried soy protein isolate were compared. Both were enzymatically treated with pepsin plus trypsin (PT) or additionally with PT plus Alcalase (PAT) for functionalisation by obtaining different partial hydrolysates. Composition, DPPH scavenging activity, digestibility and technological functionality (such as dispersibility, water-/oil-holding capacity, and zeta potential) were analysed for each protein isolate and the hydrolysates. UA-WSPI had advantages such as higher protein solubility. Enzymatic digestion of UA-WSPI resulted in the highest peptide yields and degrees of hydrolysis. Hydrolysis by the PT treatment even increased the antioxidant activity and emulsifying properties of the hydrolysate compared to UA-WSPI, whereas the soy protein isolates yielded hydrolysates of lowered antioxidant activity. Watermelon seeds proved to yield protein isolates as new functional food components, especially when applying appropriate enzyme combinations.

Orijinal dilİngilizce
Sayfa (başlangıç-bitiş)854-863
Sayfa sayısı10
DergiInternational Journal of Food Science and Technology
Hacim59
Basın numarası2
DOI'lar
Yayın durumuYayınlandı - Şub 2024

Bibliyografik not

Publisher Copyright:
© 2023 The Authors. International Journal of Food Science & Technology published by John Wiley & Sons Ltd on behalf of Institute of Food, Science and Technology (IFSTTF).

Finansman

The authors thank Ms. Birgit Greif for performing the Dumatherm runs for protein quantification. Ezgi Şenol was supported by the European Union's Erasmus+ KA103 Programme. Open Access funding enabled and organized by Projekt DEAL.

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