高等学校化学学报 ›› 2023, Vol. 44 ›› Issue (4): 20220699.doi: 10.7503/cjcu20220699

• 物理化学 • 上一篇    下一篇

双重包埋激活脂肪酶内花凝胶微球的制备与表征

张帆1,2, 郑兰兰1, 曹红1(), 程路峰2(), 李春3   

  1. 1.嘉兴学院生物与化学工程学院, 嘉兴市分子识别材料与传感技术重点实验室, 嘉兴 314001
    2.新疆医科大学药学院, 乌鲁木齐 830011
    3.清华大学化学工程系, 北京 100084
  • 收稿日期:2022-11-05 出版日期:2023-04-10 发布日期:2023-01-15
  • 通讯作者: 曹红,程路峰 E-mail:chyf_ch@126.com;lewis_clf@163.com
  • 基金资助:
    国家自然科学基金(21266029);浙江省自然科学基金(LY17B060011)

Preparation and Characterization of an Inner Flower Gel Microsphere Double-embedded with the Activated-lipase

ZHANG Fan1,2, ZHENG Lanlan1, CAO Hong1(), CHENG Lufeng2(), LI Chun3   

  1. 1.Jiaxing Key Laboratory of Molecular Recognition and Sensing,College of Biological Chemical Sciences and Engineering,Jiaxing University,Jiaxing 314001,China
    2.College of Pharmacy,Xinjiang Medical University,Urumqi 830011,China
    3.Department of Chemical Engineering,Tsing Hua University,Beijing 100084,China
  • Received:2022-11-05 Online:2023-04-10 Published:2023-01-15
  • Contact: CAO Hong, CHENG Lufeng E-mail:chyf_ch@126.com;lewis_clf@163.com
  • Supported by:
    the National Natural Science Foundation of China(21266029);the Natural Science Foundation of Zhejiang Province, China(LY17B060011)

摘要:

首先利用聚乙二醇8000(PEG8000)将脂肪酶激活为开放构象(PEG-Lip), 再将PEG-Lip与Ca3(PO4)2共结晶制得Ca3(PO4)2@PEG-Lip晶体花, 然后将晶体花包覆于海藻酸钙(CA)凝胶(Gel)微球中, 制得一种双重包埋激活脂肪酶的内花凝胶微球CA-Gel@Ca3(PO4)2@PEG-Lip. 该微球呈白色椭圆状, 直径约2 mm. 利用扫描电子显微镜(SEM)、 X射线光电子能谱(EDS)、 共聚焦显微镜(CLSM)和傅里叶变换红外光谱(FTIR)表征了其微观形貌和组成, 发现脂肪酶被包埋在Ca3(PO4)2晶体中, 形成的Ca3(PO4)2@PEG-Lip晶体花被包覆于海藻酸钙凝胶微球内的网络中. CA-Gel@Ca3(PO4)2@PEG-Lip的酶学性质研究表明, 在Ca3(PO4)2晶体和海藻酸钙凝胶的“双层铠甲”保护下, 脂肪酶的热稳定性和pH稳定性均有所改善. 利用孔径约0.5 mm的滤网即可实现对凝胶微球的快速回收; 循环利用10次后, 酶活保留率达83%, 脂肪酶的操作稳定性和重复利用性明显提高. 本文为脂肪酶在食品与医药工业中的开发利用提供了新的思路与方法.

关键词: 双重包埋, 激活脂肪酶, 内花凝胶微球, 磷酸钙晶体, 海藻酸钙凝胶

Abstract:

Lipase was first activated to an open conformation(PEG-Lip) by polyethylene glycol(PEG8000), then cocrystallized with Ca3(PO42 into Ca3(PO42@PEG-Lip crystal flowers, and then coated with calcium alginate gel to form a inner flower gel microsphere double-embedded activated-lipase[CA-Gel@Ca3(PO42@PEG-Lip]. The gel microspheres were white and oval-shaped with a diameter of about 2 mm. Characterized by scanning electron microscopy(SEM), energy dispersive spectrometer(EDS), confocal microscopy(CLSM) and fourier transform infrared spectrophotometer(FTIR), the activated lipase was embedded in Ca3(PO42 crystals, and the Ca3(PO42@PEG-Lip crystal flowers were entrapped in mesh pores of calcium alginate gel. Enzymatic properties showed that the heat resistance and the pH stability of CA-Gel@Ca3(PO42@PEG-Lip were enhanced under the protection of double armors compared to free lipase. In the repeated utilization experiment, the rapid recovery of CA-Gel@Ca3(PO42@PEG-Lip could be achieved with an aperture diameter of approximately 0.5 mm filter, and after 10 cycles, the enzyme activity was retained up to 83%, showing the obvious improvement of operational stability and reusability of the lipase. This paper provides a new idea and method for the development and utilization of lipase in food industry.

Key words: Double embedding technique, Activated-lipase, Inner flower gel microsphere, Calcium phosphate crystal, Calcium alginate gel

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