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Trang 5WtQKNKiQJR[\KyDYjWtQKFKҩWFKӭFQăQJFӫDGӏFKWKӫ\SKkQSURWHLQFRQUXӕFNK{ĈҫXWLrQҧQKKѭӣQJFӫDWKӡLJLDQWKӫ\SKkQÿӃQ'+FӫDGӏFKWKӫ\SKkQSURWHLQFRQUXӕFNK{ÿѭӧFÿiQKJLi6DXÿyҧQKKѭӣQJFӫD'+ ÿӃQKRҥWWtQKNKiQJ R[\KyDFӫD GӏFKWKӫ\SKkQ SURWHLQ WKHR SKѭѫQJ SKiS WUXQJ KzD JӕF Wӵ GR 2,2-diphenyl-1-picrylhydrazyl (DPPH) SKѭѫQJ SKiS QăQJ OӵF NKiQJ R[\ KyD NKӱ LRQ VҳW ,,, FRAP) SKѭѫQJ SKiSWUXQJ KzD JӕF Wӵ GR cation 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTSƔ+)SKѭѫQJSKiSWUXQJKzDJӕFWӵGRanion superoxide (O2Ɣ-) YjSKѭѫQJSKiSOLrQNӃWLRQFe2+ ÿѭӧFNKҧRViW&XӕLFQJҧQKKѭӣQJFӫD'+ÿӃQWtQKFKҩWFKӭFQăQJFӫDGӏFKWKӫ\SKkQSURWHLQJӗPÿӝWDQÿӝEӅQQKLӋWNKҧQăQJWҥREӑWNKҧQăQJWҥRQKNJNKҧ QăQJJLӳQѭӟF (WHC) YjNKҧQăQJJLӳGҫX (OHC) ÿѭӧFQJKLrQFӭX.ӃWTXҧFKRWKҩ\JLiWUӏ'+ FӫD GӏFKWKӫ\SKkQSURWHLQFRQ UXӕF NK{WăQJWӯÿӃQ NKLWKӡLJLDQWKӫ\SKkQNpRGjLWӯÿӃQSK~W'ӏFKWKӫ\SKkQSURWHLQFRQUXӕFNK{WKӇKLӋQKRҥWtính kháng oxy hóa FDRYӟLKRҥWWtQK WUXQJKzDJӕF'33+YjJLiWUӏ)5$3FDRQKҩWOҫQOѭӧWOjWKҩSKѫQ OҫQVRYӟLKRҥWWtQKWUXQJKzDJӕF'33+FӫDYLWDPLn C) và 74,6 ± 1,9 µM ÿѭѫQJ OѭӧQJ 7UROR[ µM TE) WKҩS KѫQ OҫQ VR YӟL JLi WUӏ)5$3FӫDYLWDPLQ& WҥLJLiWUӏ'+KRҥWWtQKWUXQJ KzDJӕFWӵGR$%76Ɣ+ và KRҥWtính WUXQJKzDJӕFWӵGR22Ɣ- FDRQKҩWYӟLJLiWUӏOҫQOѭӧWOҫQWKҩSKѫQVRYӟLFӫDKRҥWWtQKWUXQJKzDJӕFWӵGR$%76Ɣ+ FӫD vitamin C) và 90,8 ± 0,8% (1,1 OҫQWKҩSKѫQVRYӟLKRҥWWtQKWUXQJKzDJӕFO2Ɣ- FӫDYLWDPLQ& WҥLJLi WUӏ'+ ; hRҥWWtQKOLrQNӃWLRQFe2+
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Trang 6antioxidant activity and functional properties of proteolysate from dried Acetes japonicus Firstly, effect of hydrolysis time on DH of Acetes proteolysate was investigated Subsequently, effect of DH on antioxidant activity of the Acetes proteolysate based on
2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging assay, ferric reducing antioxidant power (FRAP) assay, 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) cation radical (ABTSƔ+) scavenging activity, superoxide anion radical (O2Ɣ-) scavenging activity and ferrous chelating rate was tested Finally, effect of DH on functional properties of the proteolysate including solubility, heat stability, foaming and emulsifying property, water holding capacity (WHC) and oil holding capacity (OHC) were evaluated The result indicated that DH value of the proteolysate increased from 0 to 75.8% as prolonging
hydrolysis time in range of 0 - 180 minutes The Acetes proteolysate exerted great
antioxidant activity with the highest DPPH scavenging activity and FRAP value of 22.5 ± 0.3% (1.8 times lower than that of vitamin C) and 74.6 ± 1.9 µM Trolox equipvalent (µM TE) (24.2 folds lower comparing to that of vitamin C), respectively, at DH of 66.7%; the greatest ABTSƔ+ và O2Ɣ- scavenging activity of 33.5 ± 0.1% (2.4 folds lower than that of vitamin C) and 90.8 ± 0.8% (1.1 times lower in comparison to that of vitamin C), in order, at DH value of 75.8%; the highest ferrous chelating rate of 54.5 ± 0.3% (1.7 folds lower than that of disodium ethylenediaminetetraacetate (Na2EDTA)) at DH value of
72.1% The Acetes proteoysate powder at all tested DH range displayed solubility over
55%, even after treating at 63oC for 30 minutes or 93oC for 30 seconds, in pH range from
3 to 8 Foaming capacity (FC) and foaming stability (FS) of the Acetes proteolysate with
various DH were in range 5.7 ± 80.0% and 2.9 ± 77.0%, 1.1 ± 14.5 folds and 1.1 ± 40.3 times lower than those of albumin, respectively, in the pH range of 3 ± 8 Emulsifying activity indexs (EAI) of the proteolysate were 1.3 ± 3.9 folds lower in comparison to that of sodium caseinate while their emulsifying stability indexs (ESI) were 1.4 ± 9.3 times higher than that of sodium caseinate at all DH value in the pH range of 3 ± 8 The proteolysate powder showed the highest WHC of 9.5 ± 0.3 ml water/g proteolysate powder at DH 66.7% and the greatest OHC of 3.4 ± 0.1 ml oil/g proteolysate powder at
DH 50.6% This study contributed to enhanced value of the Acetes, being protein source
to produce proteolysate which could be served as an antioxidant compound or a food additive improving food texture and sensory
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Trang 36&+ѬѪ1*.ӂ748Ҧ9¬%¬1/8Ұ1 3.1 ҦQKKѭӣng cӫa thӡi gian thӫy phân ÿӃn DH
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&iFNêWӵNKiFQKDXWKӇKLӋQVӵNKiFQKDXFyêQJKƭDWKӕQJNrS
Hình 3.1 ̪QKK˱ͧng cͯa thͥi gian thͯ\SKkQÿ͇n DH cͯa d͓ch thͯy phân protein con ru͙c khô
*LiWUӏ'+FӫDGӏFKWKӫ\SKkQSURWHLQFRQUXӕFNK{WăQJQKDQKWӯÿӃQtrong 4SK~WÿҫXFӫDTXiWUuQKWKӫ\SKkQĈLӅXQj\FyWKӇJLҧLWKtFKGRSURWHLQFRQUXӕFNK{FyQKLӅXÿLӇPSKKӧSYӟLWUXQJWkPKRҥWÿӝQJFӫDFKӃSKҭP)ODYRXU]\PH7KrP
Trang 37YjRÿy)ODYRXU]\PHOjFKӃSKҭPHQ]\PHFKӭDORҥLSURWHDVHleucine aminopeptidase A, leucine aminopeptidase 2, dipeptidyl peptidase 4, dipeptidyl peptidase 5, neutral protease 1, neutral protease 2 và alkaline protease 1 EDRJӗPFҧHQGR- và exo-peptidase [54]WKӫ\SKkQÿѭӧFQKLӅXSURWHLQ khác nhau.KLNpRGjLWKӡLJLDQWKӫ\SKkQÿӃQSK~WWӕFÿӝYjÿӝOӟQVӵWKD\ÿәLJLiWUӏ'+WKҩSKuQK 1JX\rQQKkQÿѭӧFFKROjGRVӕOѭӧQJOLrQNӃWSKKӧSYӟLWUXQJWkPWKӫ\SKkQFӫDFKӃSKҭP)ODYRXU]\PHÿmJLҧPÿiQJNӇWURQJSK~WÿҫX.ӃWTXҧWѭѫQJWӵFNJQJÿѭӧFF{QJEӕEӣL1RPDQYjFӝQJVӵ(2018) [10] NKL QJKLrQ FӭX ҧQK KѭӣQJ FӫD WKӡL JLDQ WKӫ\ SKkQ ÿӃQ '+ FӫD GӏFK WKӫ\phân protein cá WҫP 7UXQJ 4XӕF 7ӯ ÿӗ WKӏ KuQK FiF JLi WUӏ '+ JӗP 50,6%, 66,7%, 69,7%, 71,5%, 72,1% và 75,8ӭQJYӟLWKӡLJLDQWKӫ\SKkQWѭѫQJӭQJOjYjSK~WÿѭӧFFKӑQÿӇWKӵFKLӋQFiFNKҧRViWWLӃSWKHR
3.2 ҦQKKѭӣng cӫD'+ÿӃn hoҥt tính kháng oxy hóa cӫa dӏch thӫy phân protein con ruӕc khô
3.2.1 HoҥWWtQKNKiQJR[\KyDWKHRFѫFKӃ cho electron
*ӕFWӵGR'33+Oj PӝWWURQJQKӳQJJӕFWӵGREӅQPjXWtPYjFyÿӝKҩSWKXFӵFÿҥLWҥLEѭӟFVyQJQP.KLFyPһWFKҩWNKiQJR[\KyDJӕFWӵ GR'33+EӏWUXQJKzDGRQKұQ PӝW HOHFWURQWӯFKҩWNKiQJ R[\KyD ӃWTXҧ OjÿӝKҩS WKXWҥLEѭӟFVyQJQPJLҧPYjPjXFӫDGXQJGӏFKFKX\ӇQWӯWtPVDQJYjQJ[55]
3KѭѫQJSKiS)5$3ÿѭӧFGQJQKѭSKѭѫQJSKiSWKӭKDLÿӇÿiQKJLiҧQKKѭӣQJFӫD'+ÿӃQNKҧQăQJFKRHOHFWURQFӫDGӏFKWKӫ\SKkQSURWHLQFRQUXӕFNK{ 7URQJSKѭѫQJSKiS )5$3 FKҩW NKiQJ R[\ KyD KRҥW ÿӝQJ QKѭ PӝW FKҩW NKӱ NKӱ SKӭF VҳW ,,, tripyridyl triazine (Fe(III)-TPTZ) WKjQK SKӭF )H,, -TPTZ 0ӭF ÿӝ NKӱ ÿѭӧF ÿiQK JLiWK{QJTXDVӵWKD\ÿәLÿӝKҩSWKXӣEѭӟFVyQJQP[56]
Hình 3.2 FKRWKҩ\KRҥWWtQKWUXQJKzDJӕF'33+YjJLiWUӏ)5$3ÿӅXWăQJNKLJLiWUӏDH WăQJWӯÿӃQÿҥWJLiWUӏFӵFÿҥLOҫQOѭӧWOj% (WKҩSKѫQOҫQso YӟLKRҥWWtQKWUXQJKzDJӕF'33+FӫDYLWDPLQ&) và 74,6 ± 1,9 07(WKҩSKѫQOҫQ VR YӟL JLi WUӏ )5$3 FӫD YLWDPLQ &