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Antioxidant and anticancer activities of enzymatic eel (monopterus sp) protein hydrolysate as influenced by different molecular weight.

Authors :
Halim, Nura Ruhaya Abdul
Azlan, Azrina
Yusof, Hayati Mohd
Sarbon, Norizah Mhd
Source :
Biocatalysis & Agricultural Biotechnology; Oct2018, Vol. 16, p10-16, 7p
Publication Year :
2018

Abstract

Abstract This study aims to investigate the antioxidant and anticancer properties of fractionated eel protein hydrolysate (EPH) as well as qualitatively determine its free fatty acids. The eel flesh was enzymatically hydrolyzed and fractionated through membrane filter (10 kDa, 5 kDa and 3 kDa). The lipid peroxidation assays and mechanisms of antioxidant activity (reducing power, ferrous ion chelating activity and 1, 1-diphenylpicrylhydrazyl (DPPH) radical scavenging activity) of fractionated EPH were determined. The anticancer activity was determined by 3–4, 5-dimethylthiazol-2-yl-2, 5-diphenyltetrazolium bromide (MTT) assay using MCF-7 cell lines. Free fatty acids in eel flesh and EPH were determined using gas chromatography. The results obtained showed that 3 kDa EPH possessed the highest inhibition of lipid peroxidation, reducing power, DPPH scavenging activity and anticancer activity. Moreover, the changes of unsaturated fatty acids during hydrolysis process resulting in more stable hydrolysate towards oxidation. Based on the mechanisms of antioxidant activity conducted, this study found that the EPH had more ability as primary antioxidant than secondary antioxidant. Highlights • 3 kDa EPH possessed the highest antioxidant and anticancer activity. • Hydrolysis process resulted in more stable hydrolysate towards oxidation. • EPH demonstrated greater ability as a primary antioxidant than as a secondary antioxidant. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18788181
Volume :
16
Database :
Supplemental Index
Journal :
Biocatalysis & Agricultural Biotechnology
Publication Type :
Academic Journal
Accession number :
133093033
Full Text :
https://doi.org/10.1016/j.bcab.2018.06.006