Abstract

Phenols are widely present in plants and often are co-extracted in plant protein extracts, while such components could influence the protein's interface and foam stabilising properties. In this study, the influence of rapeseed phenol sinapic acid (SA) on the interfacial and foaming properties of a well characterised model protein, whey protein isolate (WPI), was investigated. WPI formed strong viscoelastic interfacial layers, and addition of SA reduced the surface dilatational modulus by 25%. Turning SA into its active oxidised form in the WPI-SA mixtures led to protein aggregation, resulting in a further decrease of the modulus by 40%. Removal of unbound phenols induced a slight increase of the dilatational modulus, but the interfacial layer strength did not fully recover to that made with pure WPI, suggesting binding of phenols to proteins, and thus influencing the protein interface stabilising properties. Foams stabilised by WPI-SA mixtures had a shorter foam half-life time (130–180 min) than foams stabilised by pure WPI (260 min). Our data are thus in line with the observation that a lower surface dilatational modulus leads to a lower foam stability. Yet, the foam stability did not recover to the original values of pure WPI-stabilised foams after removal of unbound phenols. In conclusion, the presence of SA resulted in a decrease in interfacial layer strength and foam stability. We conclude that in producing protein extracts from rapeseed or other phenol-rich plant sources, the presence and oxidation of phenols should thus be considered.

Highlights

  • One of the challenges in utilizing plant protein extracts as functional food ingredients is the naturally present phenols

  • The whey protein isolate used in this study is a mixture of proteins with β-lactoglobulin (74%) and α-lactal­ bumin (12.5%) as the most abundant ones

  • Interfacial and foaming properties of whey protein isolate were studied in the presence of sinapic acid

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Summary

Introduction

One of the challenges in utilizing plant protein extracts as functional food ingredients is the naturally present phenols. Rapeseed proteins have promising emulsifying (Cheung, Wanasundara, & Nick­ erson, 2014; Ntone, Bitter, & Nikiforidis, 2020; Tan, Mailer, Blanchard, & Agboola, 2011), foaming Yang, Faber, et al, 2020), and gelling properties (Tan, Mailer, Blanchard, Agboola, & Day, 2014), but rapeseed may contain up to 3% of phenols (Wanasundara, 2011). The effects of rapeseed phenols on protein functionality (e.g., gelling, emulsifying, and foaming properties) are not yet well understood, while it is key to understand such in­ teractions in the utilization of phenol-rich plant sources in food systems. The removal of phenols from rapeseed proteins requires multiple washing steps with organic solvents, resulting in a phenol removal of 75–90% and unknown effects on the protein structure and properties (Das Purkayastha et al, 2014; Xu & Diosady, 2002)

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