Antioxidant activities of sunflower protein hydrolysates treated with dual-frequency ultrasonic: Optimization study
Journal of Food Process Engineering • 2019
معلومات البحث
المؤلفون
Mokhtar Dabbour; Ronghai He; Benjamin Mintah; Haile Ma
الكلمات المفتاحية
Not Available
المجلة العلمية
Journal of Food Process Engineering
الناشر
Wiley
المجلد
42
العدد
5
الصفحات
e13084
publication.type
International
رابط البحث
Open Link
المواد المرفقة
Not Available
الملخص
In this study, ultrasound pretreatments of sunflower-meal protein (SMP) to yield high antioxidant
capacity from its hydrolysates by response surface methodology were optimized.
Optimization of experimental conditions was achieved to examine the impact of temperature,
solvent-solid ratio and sonication time on antioxidant capacities of SMP hydrolysates
with Box–Behnken's design. Quadratic models of DPPH-scavenging activity (DPPHSA),
hydroxyl-radical scavenging activity (HRSA), and Cu2+ and Fe2+ chelating activity (Cu2+-CA
and Fe2+-CA) were developed, and their coefficients observed from multiple-regression
analysis. ANOVA indicated that time was highly significant (p < .01) on all experimental
responses. The best experimental point of DPPHSA, HRSA, Cu2+-CA, and Fe2+-CA was
accessed at 42.50C, 18.16 mL/g and 26.52 min and the predicted data for these
responses were 52.09, 70.05, 50.85, and 43.35%, respectively. Outcome of verification
experiment was reliable with predicted data for all responses. Additionally, DPPHSA,
HRSA, Cu2+-CA, and Fe2+-CA of pretreated hydrolysate improved (p < .05) by 17.41,
20.00, 14.72, and 26.41%, respectively over nonsonicated hydrolysate. Amino acid content
and hydrophobicity of SMP hydrolysate at the optimum sonication condition were
analyzed. Analyses indicated that ultrasonication could facilitate the releasing/unfolding of
hydrophobic amino acids from SMP over nonsonicated samples during enzymolysis with
high antioxidative capacity.
capacity from its hydrolysates by response surface methodology were optimized.
Optimization of experimental conditions was achieved to examine the impact of temperature,
solvent-solid ratio and sonication time on antioxidant capacities of SMP hydrolysates
with Box–Behnken's design. Quadratic models of DPPH-scavenging activity (DPPHSA),
hydroxyl-radical scavenging activity (HRSA), and Cu2+ and Fe2+ chelating activity (Cu2+-CA
and Fe2+-CA) were developed, and their coefficients observed from multiple-regression
analysis. ANOVA indicated that time was highly significant (p < .01) on all experimental
responses. The best experimental point of DPPHSA, HRSA, Cu2+-CA, and Fe2+-CA was
accessed at 42.50C, 18.16 mL/g and 26.52 min and the predicted data for these
responses were 52.09, 70.05, 50.85, and 43.35%, respectively. Outcome of verification
experiment was reliable with predicted data for all responses. Additionally, DPPHSA,
HRSA, Cu2+-CA, and Fe2+-CA of pretreated hydrolysate improved (p < .05) by 17.41,
20.00, 14.72, and 26.41%, respectively over nonsonicated hydrolysate. Amino acid content
and hydrophobicity of SMP hydrolysate at the optimum sonication condition were
analyzed. Analyses indicated that ultrasonication could facilitate the releasing/unfolding of
hydrophobic amino acids from SMP over nonsonicated samples during enzymolysis with
high antioxidative capacity.
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