食品研究与开发
食品研究與開髮
식품연구여개발
FOOD RESEARCH AND CEVELOPMENT
2014年
15期
64-67,68
,共5页
对虾下脚料蛋白%酶解%超声波%水解度
對蝦下腳料蛋白%酶解%超聲波%水解度
대하하각료단백%매해%초성파%수해도
prawn leftover protein%enzymatic hydrolysis%ultrasonic%degree of hydrolysis
采用超声波间歇协助胰蛋白酶水解对虾下脚料蛋白制备低分子肽。以水解度为指标,利用Box-Behnken中心组合设计原理和响应面分析法,对酶解工艺条件进行了优化,建立了加酶量、超声波处理次数(时间)、酶解温度与水解度之间的数学模型。结果表明,最佳工艺条件为:加酶量为46.42 kat/g,超声处理次数为3次,每次5 min,间歇10 min,酶解温度为44.3℃,在此条件下水解度为62.21%,与理论计算值60.65%基本一致。水解产物中必需氨基酸含量占氨基酸总量的44.5%;构成肽的氨基酸占总氨基酸的比例为85.6%,低分子肽是蛋白水解液的主要成分。
採用超聲波間歇協助胰蛋白酶水解對蝦下腳料蛋白製備低分子肽。以水解度為指標,利用Box-Behnken中心組閤設計原理和響應麵分析法,對酶解工藝條件進行瞭優化,建立瞭加酶量、超聲波處理次數(時間)、酶解溫度與水解度之間的數學模型。結果錶明,最佳工藝條件為:加酶量為46.42 kat/g,超聲處理次數為3次,每次5 min,間歇10 min,酶解溫度為44.3℃,在此條件下水解度為62.21%,與理論計算值60.65%基本一緻。水解產物中必需氨基痠含量佔氨基痠總量的44.5%;構成肽的氨基痠佔總氨基痠的比例為85.6%,低分子肽是蛋白水解液的主要成分。
채용초성파간헐협조이단백매수해대하하각료단백제비저분자태。이수해도위지표,이용Box-Behnken중심조합설계원리화향응면분석법,대매해공예조건진행료우화,건립료가매량、초성파처리차수(시간)、매해온도여수해도지간적수학모형。결과표명,최가공예조건위:가매량위46.42 kat/g,초성처리차수위3차,매차5 min,간헐10 min,매해온도위44.3℃,재차조건하수해도위62.21%,여이론계산치60.65%기본일치。수해산물중필수안기산함량점안기산총량적44.5%;구성태적안기산점총안기산적비례위85.6%,저분자태시단백수해액적주요성분。
The protein of prawn leftover was hydrolyzed with trypsin assisted by intermittent ultrasonic method for preparing low molecular weight peptides. Taking hydrolysis degree as response values, the mathematical regression model of the relationships between the studied factors and the degree of hydrolysis of protein was constructed by means of the principles of Box-Benheken central composite experimental design and response surface analysis. Results showed that the optimum hydrolysis conditions was based on trypsin-catalyzed reaction by intermittent treatment with ultrasonic for 3 times at 44.3℃and 46.42 kat/g protein enzyme dose, 5 min every time and 10 min intermittent. Under these conditions, the degree of hydrolysis was 62.21%, which was close to the estimated value 60.65%obtained by using regression model. The hydrolysate contains essential amino acids, whose content was 44.5%of the total amino acids. The amino acids constituted peptides were 85.6%of the total amino acids. The low molecular weight peptides were the main components of hydrolysate.