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中国精品科技期刊2020
吕乐, 丁慧璞, 胡伟, 刘利萍, 王志江. 金枪鱼粉的酶解工艺及其酶解产物功能活性研究[J]. 食品工业科技, 2020, 41(3): 168-174. DOI: 10.13386/j.issn1002-0306.2020.03.029
引用本文: 吕乐, 丁慧璞, 胡伟, 刘利萍, 王志江. 金枪鱼粉的酶解工艺及其酶解产物功能活性研究[J]. 食品工业科技, 2020, 41(3): 168-174. DOI: 10.13386/j.issn1002-0306.2020.03.029
LV Le, DING Hui-pu, HU Wei, LIU Li-ping, WANG Zhi-jiang. Study on Enzymatic Hydrolysis of Tuna Powder and Functional Activity of Enzymatic Hydrolysis Products[J]. Science and Technology of Food Industry, 2020, 41(3): 168-174. DOI: 10.13386/j.issn1002-0306.2020.03.029
Citation: LV Le, DING Hui-pu, HU Wei, LIU Li-ping, WANG Zhi-jiang. Study on Enzymatic Hydrolysis of Tuna Powder and Functional Activity of Enzymatic Hydrolysis Products[J]. Science and Technology of Food Industry, 2020, 41(3): 168-174. DOI: 10.13386/j.issn1002-0306.2020.03.029

金枪鱼粉的酶解工艺及其酶解产物功能活性研究

Study on Enzymatic Hydrolysis of Tuna Powder and Functional Activity of Enzymatic Hydrolysis Products

  • 摘要: 为了对金枪鱼粉进行深加工开发,本文研究金枪鱼粉的酶解工艺,并对其酶解液进行功效性评价。以水解度为指标筛选酶制剂,运用响应面试验优化酶解工艺参数,并对酶解液的总还原力、自由基清除率、酪氨酸酶抑制率、以及对大肠杆菌的抗菌性进行测试。结果表明以碱性蛋白酶酶解金枪鱼粉的最佳条件为料液比1:5(g:mL)、加酶量1×104 U·g-1、温度55℃、时间8 h、pH10.5,在此条件下水解度为29.20%±0.08%、氨基酸态氮含量为7.57 mg·mL-1。酶解液对羟自由基有较好的清除率,且清除率随氨基态氮浓度增加而增强;当氨基态氮浓度为7.57 mg·mL-1时,酶解液的总还原力与0.4 mg·mL-1维生素C接近;酶解液对酪氨酸酶的抑制作用随氨基态氮浓度增加其抑制作用增强,且IC50=3.44 mg·mL-1。酶解液对大肠杆菌也有一定的抑制作用。本研究结果为金枪鱼粉的高值化开发提供了实验基础。

     

    Abstract: In order to develop the deep processing of tuna powder,the enzymatic hydrolysis technology of tuna meal was studied and the efficacy of enzymatic hydrolysate was evaluated. The enzymatic preparation was screened with the degree of hydrolysis as the index,and the technological parameters of enzymatic hydrolysis were optimized by response surface test design. The total reducing power,free radical scavenging rate,tyrosinase inhibitory rate and the antimicrobial activity of the enzymatic hydrolysate were tested. The results showed that the optimum conditions for enzymatic hydrolysis of tuna meal with alkaline protease were as follows:Ratio of feed to liquid 1:5 (g:mL),amount of enzymatic addition 1×104 U·g-1,temperature 55℃,time 8 h and pH10.5.Under these conditions,the degree of hydrolysis was 29.20%±0.08%,and the content of amino acid nitrogen was 7.57 mg·mL-1. The hydrolysate had a good scavenging rate for hydroxyl radicals and increased with the increase of ammonia ground nitrogen concentration. The total reducing power of the hydrolysate was close to that of vitamin C of 0.4 mg·mL-1 when the concentration of amino nitrogen was 7.57 mg·mL-1.The inhibitory effect of enzymatic hydrolysate on tyrosinase was enhanced with the increase of amino nitrogen concentration and its IC50 was 3.44 mg·mL-1. The enzymolysis solution also had a certain inhibitory effect on E. coli. The results of this study provide an experimental basis for the high-value development of tuna powder.

     

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