食品科学 ›› 2013, Vol. 34 ›› Issue (9): 210-215.doi: 10.7506/spkx1002-6630-201309043

• 生物工程 • 上一篇    下一篇

脂肪酶在尼龙网上的固定化及其酶学性质研究

赵 磊,唐 婧,王成涛*   

  1. 北京工商大学 食品添加剂与配料北京高校工程研究中心,北京市食品风味化学重点实验室,北京 100048
  • 收稿日期:2012-08-20 修回日期:2013-03-15 出版日期:2013-05-15 发布日期:2013-05-07
  • 通讯作者: 王成涛 E-mail:wct5566@163.com
  • 基金资助:

    北京市教育委员会科技计划面上项目(KM201210011008);国家自然科学基金青年科学基金项目(31201324);
    学科与研究生教育——学科建设综合计划项目(PXM2012_014213_000059)

Immobilization of Candida sp. Lipase on Nylon Net and Its Enzymatic Characteristics

ZHAO Lei,TANG Jing,WANG Cheng-tao*   

  1. Beijing Key Laboratory of Flavor Chemistry, Beijing Higher Institution Engineering Research Center of Food Additives and
    Ingredients, Beijing Technology and Business University, Beijing 100048, China
  • Received:2012-08-20 Revised:2013-03-15 Online:2013-05-15 Published:2013-05-07
  • Contact: Wang Cheng-Tao E-mail:wct5566@163.com

摘要:

以尼龙网为载体,戊二醛为交联剂制备固定化脂肪酶(Candida sp. 99-125),并对固定化条件及固定化酶的酶学性质进行研究。结果表明,最适固定化条件为:戊二醛体积分数3%、交联时间60min、脂肪酶质量浓度10mg/mL、固定化时间6h。与游离酶相比,固定化脂肪酶的最适温度从45℃提高至50℃,最适pH值相同,均为7.0,并在pH5.0~7.0范围内均有非常高的活力。固定化脂肪酶相对于游离酶具有更好的热稳定性和pH值稳定性,并具有良好的操作稳定性,其重复操作5次后相对酶活力仍保持在80%左右。固定化脂肪酶的Km值(0.57mol/L)和最大反应速率Vmax(0.29×10-3mol/(L·s))显著高于游离酶,对底物的亲和力较游离酶弱。

关键词: 固定化酶, 尼龙网, 戊二醛, 稳定性, 动力学

Abstract:

Lipase (Candida sp. 99-125) was immobilized on nylon net by glutaraldehyde as cross-linking agent. Effects of
various parameters on the activity of immobilized lipase and characteristics of immobilized lipase were investigated. The
maximum enzyme activity achieved at the following conditions: glutaraldehyde concentration of 3%, cross-linking time of
60 min, enzyme concentration of 10 mg/mL, and immobilized time of 6 h. The optimal temperature of immobilized lipase
shifted from 45 ℃ to 50 ℃, compared with free lipase. The immobilized lipase maintained high activity in a broad pH range
of 5.0 to 7.0, with optimum pH at 7.0, which was identical to that of the free lipase. Thermal, pH, and operational stabilities
of lipase were greatly improved after immobilization onto nylon net. Immobilized lipase retained about 80% of the initial
activity after fifth repeated use. The Km (0.57 mol/L) and Vmax (0.29 × 10-3 mol/(L•s)) of immobilized lipase using olive oil as
substrate was significantly higher as compared to free lipase. The immobilization of lipase decreased its affinity to substrate
as compared to free lipase.

Key words: immobilized lipase, Nylon net, glutaraldehyde, stability, kinetics

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