食品研究与开发
食品研究與開髮
식품연구여개발
FOOD RESEARCH AND CEVELOPMENT
2014年
24期
5-9
,共5页
孙琳琳%闵伟红%冷帅辰%李京京%刘景圣%郑鸿雁
孫琳琳%閔偉紅%冷帥辰%李京京%劉景聖%鄭鴻雁
손림림%민위홍%랭수신%리경경%류경골%정홍안
长白山核桃楸%分离蛋白%响应面%抗氧化活性
長白山覈桃楸%分離蛋白%響應麵%抗氧化活性
장백산핵도추%분리단백%향응면%항양화활성
Juglans mandshurica Maxim%protein isolate%response surface methodology%antioxidant activity
以长白山核桃楸种仁分离蛋白为原料,采用Box-Benhnken响应面法对影响还原能力的主要因素pH、温度、加酶量和底物浓度进行研究。确定其最佳工艺参数为:pH7.6,酶解温度50℃,加酶量4510 U/g,底物浓度4.6%,时间4 h,该条件下其还原能力为0.35,水解度为16.50%。抗氧化活性试验表明,随着分离蛋白酶解产物浓度的增加,对DPPH、ABTS、·OH的清除作用及还原能力逐渐增加。当酶解产物浓度达到0.8 mg/mL时,对ABTS的清除率为VC的100%,当浓度达到1.2 mg/mL时,对DPPH的清除率达到相同浓度VC的90.08%。浓度继续增加到15 mg/mL时,对·OH的清除作用为VC的94.56%;这说明优化后的核桃楸种仁分离蛋白酶解产物对DPPH和ABTS具有较强的清除作用,对·OH的清除作用比VC弱。
以長白山覈桃楸種仁分離蛋白為原料,採用Box-Benhnken響應麵法對影響還原能力的主要因素pH、溫度、加酶量和底物濃度進行研究。確定其最佳工藝參數為:pH7.6,酶解溫度50℃,加酶量4510 U/g,底物濃度4.6%,時間4 h,該條件下其還原能力為0.35,水解度為16.50%。抗氧化活性試驗錶明,隨著分離蛋白酶解產物濃度的增加,對DPPH、ABTS、·OH的清除作用及還原能力逐漸增加。噹酶解產物濃度達到0.8 mg/mL時,對ABTS的清除率為VC的100%,噹濃度達到1.2 mg/mL時,對DPPH的清除率達到相同濃度VC的90.08%。濃度繼續增加到15 mg/mL時,對·OH的清除作用為VC的94.56%;這說明優化後的覈桃楸種仁分離蛋白酶解產物對DPPH和ABTS具有較彊的清除作用,對·OH的清除作用比VC弱。
이장백산핵도추충인분리단백위원료,채용Box-Benhnken향응면법대영향환원능력적주요인소pH、온도、가매량화저물농도진행연구。학정기최가공예삼수위:pH7.6,매해온도50℃,가매량4510 U/g,저물농도4.6%,시간4 h,해조건하기환원능력위0.35,수해도위16.50%。항양화활성시험표명,수착분리단백매해산물농도적증가,대DPPH、ABTS、·OH적청제작용급환원능력축점증가。당매해산물농도체도0.8 mg/mL시,대ABTS적청제솔위VC적100%,당농도체도1.2 mg/mL시,대DPPH적청제솔체도상동농도VC적90.08%。농도계속증가도15 mg/mL시,대·OH적청제작용위VC적94.56%;저설명우화후적핵도추충인분리단백매해산물대DPPH화ABTS구유교강적청제작용,대·OH적청제작용비VC약。
With protein isolate from Juglans mandshurica Maxim kernel in Changbai mountain as the raw material,response surface methodology was applied to optimize the hydrolysis conditions (including pH, temperature, enzyme dosage, and substrate concentration) with reducing power ability as index. The optimum extraction conditions are as follows: pH value of 7. 6, substrate concentration of 4. 6 %, enzyme dosage of 4 510 U/g, enzymolysis temperature of 50℃, and time of 4 h. On this condition, the reducing power ability was 0. 35, the degree of hydrolysis was 16. 50%. The results of antioxidant tests showed that scavenging activity on DPPH, ABTS,·OH and reducing power ability increased with increasing enzymatic hydrolysate concentration. The scavenging activity of enzymatic hydrolysate on DPPH and ABTS was 90. 08%and 100%of VC at 1. 2 mg/mL and 0. 8 mg/mL, the scavenging activity on ·OH was 94. 56%of VC at 15 mg/mL. These demonstrated that the scavenging activity of enzymatic hydrolysate on DPPH and ABTS are strong, the scavenging activity on·OH are weaker than those of VC.