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中国精品科技期刊2020
李雨奇, 李博, 王成涛. 鱼皮抗血小板胶原肽的功效评价及酶法制备工艺优化[J]. 食品工业科技, 2019, 40(18): 185-193. DOI: 10.13386/j.issn1002-0306.2019.18.030
引用本文: 李雨奇, 李博, 王成涛. 鱼皮抗血小板胶原肽的功效评价及酶法制备工艺优化[J]. 食品工业科技, 2019, 40(18): 185-193. DOI: 10.13386/j.issn1002-0306.2019.18.030
LI Yu-qi, LI Bo, WANG Cheng-tao. Efficacy Evaluation and Optimization of Enzymatic Preparation Process of Anti-platelet Collagen Peptides from Fish Skin[J]. Science and Technology of Food Industry, 2019, 40(18): 185-193. DOI: 10.13386/j.issn1002-0306.2019.18.030
Citation: LI Yu-qi, LI Bo, WANG Cheng-tao. Efficacy Evaluation and Optimization of Enzymatic Preparation Process of Anti-platelet Collagen Peptides from Fish Skin[J]. Science and Technology of Food Industry, 2019, 40(18): 185-193. DOI: 10.13386/j.issn1002-0306.2019.18.030

鱼皮抗血小板胶原肽的功效评价及酶法制备工艺优化

Efficacy Evaluation and Optimization of Enzymatic Preparation Process of Anti-platelet Collagen Peptides from Fish Skin

  • 摘要: 本实验用鲢鱼皮为原料,通过酶法开发一种以Gly-Pro-Arg(GPR)、Gly-Pro-Arg-Gly(GPRG)和Gly-Pro-Arg-Gly-Pro(GPRGP)等抗血小板肽为活性成分的可预防血栓的第三代功能性食品。首先利用比浊法评价了三条肽的抗血小板功效,发现三者均可剂量依赖性地抑制二磷酸腺苷(ADP)诱导的血小板聚集。之后用复合蛋白酶对鲢鱼皮胶原进行水解,以产物中目标抗血小板肽含量为响应值,依次通过Plackett-Burman试验、爬坡试验和Box-Behnken试验确定了最优的酶解条件为底物浓度7%、初始pH8、加酶量1930 U/g、酶解时间8 h;在此条件下得到的产品中三条目标活性肽含量为6.80%;其抑制血小板聚集的IC50值为1.669 mg/mL。产品中总氮含量为17.430%±0.065%(以干基计),多肽含量为92.16%±0.27%(以干基计),羟脯氨酸含量为6.42%±0.03%,相对分子量<1000 Da肽段所占比例为94.95%,灰分3.92%,干燥失重0.93%,这些理化指标均符合相关国家标准中的规定。因此利用本结论可以得到一种以GPR、GPRG和GPRGP等肽为活性成分的抗血小板功能性食品。

     

    Abstract: In order to develop a novel functional food with Gly-Pro-Arg(GPR),Gly-Pro-Arg-Gly(GPRG)and Gly-Pro-Arg-Gly-Pro(GPRGP)as the active ingredient,the raw material silver carp(Hypophthalmichthys molitrix)skin hydrolyzed by enzyme that could prevent thrombosis. Firstly,the efficacies of anti-platelet activity of three peptides were evaluated by turbidimetry. It was found that three peptides inhibited ADP-induced platelet aggregation as a dose-dependent manner. Then,the collagen of silver carp skin was hydrolyzed by compound enzyme. Contents of the three anti-platelet peptides in the hydrolysate as the response value was measured. The optimum enzymatic conditions were successively determined by Plackett-Burman test,steepest ascent and Box-Behnken test. Finally,the optimal enzymatic conditions were determined as followed:The substrate concentration of 7%,initial pH8,enzyme concentration of 1930 U/g and hydrolysis time of 8 h. The anti-platelet peptides content(the sum of GPR,GPRG and GPRGP)of the final products obtained under this condition was 6.80%. The IC50 of inhibiting platelet aggregation was 1.669 mg/mL. The physicochemical indexes of the final products were as follow:The total nitrogen content of the product was 17.430±0.065%(on a dry basis),the peptide content was 92.16%±0.27%(based on a dry basis),the hydroxyproline content was 6.42%±0.03%,the peptide(1000 Da)was 94.95%,the ash was 3.92%,and the loss on drying was 0.93%. These indexes of the final products were in compliance with the relevant standards. In summary,an anti-platelet functional food with GPR,GPRG and GPRGP as the active ingredients could be obtained by using the method of this study.

     

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