食品科学 ›› 2018, Vol. 39 ›› Issue (6): 155-161.doi: 10.7506/spkx1002-6630-201806025

• 生物工程 • 上一篇    下一篇

响应面试验优化双酶酶解法制备鱼鳞抗菌肽工艺及其抑菌性能分析

施永清1,王巧巧1,吴丹丽1,李晓玉1,蔡路昀2,励建荣2,*   

  1. (1.浙江工商大学食品与生物工程学院,浙江?杭州 310018;2.渤海大学食品科学与工程学院,辽宁?锦州 121013)
  • 出版日期:2018-03-25 发布日期:2018-03-14
  • 基金资助:
    食品科学与工程浙江省重中之重一级学科资助项目(2017SIAR221);浙江工商大学大学生科研创新基金项目(CX201710009); 浙江工商大学2015年食品学院卓越食品人才(学生)科技培育项目(20151214); 辽宁省科技厅农业攻关及成果产业化项目(2015103020)

Optimization of Preparation of Antimicrobial Peptides by Two-Step Enzymatic Hydrolysis of Fish Scales Using Response Surface Methodology and Antimicrobial Activity of Purified Antimicrobial Peptide

SHI Yongqing1, WANG Qiaoqiao1, WU Danli1, LI Xiaoyu1, CAI Luyun2, LI Jianrong2,*   

  1. (1. School of Food Science and Biotechnology, Zhejiang Gongshang University, Hangzhou 310018, China; 2. College of Food Science and Engineering, Bohai University, Jinzhou 121013, China)
  • Online:2018-03-25 Published:2018-03-14

摘要: 采用双酶酶解法制备鱼鳞抗菌肽,进行酶筛选并通过响应面法优化酶解条件;通过葡聚糖凝胶G-25分离纯化酶解液,研究有效抑菌组分对不同菌的最小抑菌浓度(minimum inhibitory concentration,MIC)。结果表明,当采用碱性蛋白酶结合酸性蛋白酶分步酶解鱼鳞,底物质量浓度为30?g/100?mL时,最适酶解条件为碱性蛋白酶在pH?9.5时首次酶解,酶解时间62?min,酶解温度55?℃;酸性蛋白酶在pH?3.0时再次酶解,酶解时间3?h,酶解温度34.4?℃。此条件下制备的酶解液对副溶血性弧菌的抑菌圈直径为27.72?mm,与预测值基本相符。酶解液经层析后,其抑菌性G2组分对假单胞菌和希瓦氏菌的MIC为1.56?μg/mL,对金黄色葡萄球菌、枯草芽孢杆菌、大肠杆菌、沙门菌及副溶血性弧菌的MIC为6.25?μg/mL。可见,双酶酶解法制备的鱼鳞抗菌肽具有较强的抑菌性。

关键词: 酶解, 鱼鳞, 抗菌肽, 响应面法, 抑菌性

Abstract: This study aimed to prepare antimicrobial peptides (AMPs) by two-step enzymatic hydrolysis of crucian carp scales and to evaluate the antimicrobial activity of purified AMPs. Hydrolysis conditions were optimized by one-factor-at-a-time method and response surface methodology based on the diameter of inhibition zones against tested bacteria. The enzymatic hydrolysate prepared using optimized conditions was then purified by Sephadex G-25 column chromatography, yielding only a single peak (G2) with antimicrobial activity. The minimum inhibitory concentration (MIC) of G2 was tested. The results indicated that a solid-to-liquid ratio of 30 g/100 mL and sequential hydrolysis with alcalase at pH 9.5 and 55 ℃ for 62 min followed by acid protease at pH 3.0 and 34.4 ℃ for another 3 h were found to be the optimal conditions to obtain a greater diameter of inhibition zone against Vibrio parahemolyticus of 27.72 mm, which was well matched with the predicted value (27.37 mm). The MIC of G2 was 1.56 μg/mL against Pseudomonas and Shewanella putrefaciens, and 6.25 μg/mL against Escherichia coli, Staphylococcus aureus, Salmonella choleraescens, V. parahemolyticus and Bacillus subtilis. In conclusion, AMPs derived from freshwater fish scales by stepwise enzymatic hydrolysis possess strong antimicrobial activity.

Key words: enzymatic hydrolysis, fish scales, antimicrobial peptides, response surface methodology, antimicrobial activity

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