Antioxidant properties of Australian canola meal protein hydrolysates.

Food Chem

E. H. Graham Centre for Agricultural Innovation, Charles Sturt University, Locked Bag 588, Wagga, NSW 2678, Australia; School of Agricultural and Wine Sciences, Charles Sturt University, Locked Bag 588, Wagga, NSW 2678, Australia; Department of Human Nutritional Sciences, The Richardson Center for Functional Foods and Nutraceuticals, University of Manitoba, Winnipeg R3T 2N2, Canada. Electronic address:

Published: March 2014

Antioxidant activities of canola protein hydrolysates (CPHs) and peptide fractions prepared using five proteases and ultrafiltration membranes (1, 3, 5, and 10kDa) were investigated. CPHs had similar and adequate quantities of essential amino acids. The effective concentration that scavenged 50% (EC50) of the ABTS(+) was greatest for the <1kDa pancreatin fraction at 10.1μg/ml. CPHs and peptide fractions scavenged DPPH(+) with most of the EC50 values being <1.0mg/ml. Scavenging of superoxide radical was generally weak, except for the <1kDa pepsin peptide fraction that had a value of 51%. All CPHs inhibited linoleic acid oxidation with greater efficiency observed for pepsin hydrolysates. The oxygen radical absorbance capacity of Alcalase, chymotrypsin and pepsin hydrolysates was found to be better than that of glutathione (GSH) (p<0.05). These results show that CPHs have the potential to be used as bioactive ingredients in the formulation of functional foods against oxidative stress.

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Source
http://dx.doi.org/10.1016/j.foodchem.2013.09.081DOI Listing

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