Chemical Industry and Engineering Progree ›› 2015, Vol. 34 ›› Issue (06): 1526-1531.DOI: 10.16085/j.issn.1000-6613.2015.06.004

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Progress of concentrating enzyme

BAI Jing1, HUANG Huijie1, CHEN Junying1, CHANG Chun1, FANG Shuqi1, LI Hongliang1, ZHANG Lu1, YAN Deran2   

  1. 1 School of Chemical Engineering and Energy, Zhengzhou University, Zhengzhou 450001, Henan, China;
    2 State Key Laboratory of Motor Vehicle Biofuel Technology, Nanyang 473000, Henan, China
  • Received:2014-10-10 Revised:2014-12-22 Online:2015-06-05 Published:2015-06-05

酶制剂浓缩方法研究进展

白净1, 黄会杰1, 陈俊英1, 常春1, 方书起1, 李洪亮1, 张璐1, 闫德冉2   

  1. 1 郑州大学化工与能源学院, 河南 郑州 450001;
    2 车用生物燃料技术国家重点实验室, 河南 南阳 473000
  • 通讯作者: 陈俊英,副教授,研究方向为可再生能源。E-mail:chenjy@zzu.edu.cn。
  • 作者简介:白净(1975—),男,博士,硕士生导师,从事新能源研究工作。E-mail:baijing@zzu.edu.cn
  • 基金资助:
    国家自然科学基金(U1404519)、河南省科技攻关计划(132102310042)及车用生物燃料技术国家重点实验室开放基金(KFKT2013012)项目。

Abstract: Presently, the enzyme concentrating method as the critical procedure in production of enzyme has many disadvantages, including complex process and high energy consumption. The common methods, including evaporation, ultrafiltration, adsorption, freezing are compared with the latest methods, including ionic liquid, hydrate, and their advantages and disadvantages are analyzed. Evaporation technology is mature but consumes excessive energy and keeps less enzyme activity. Ultrafiltration and adsorption consume less energy but have high material costs and are difficult to regenerate. The disadvantage of freezing concentration is the limit of concentration, though it can keep more activity. Concentrating by the ionic liquid method is easy to scale up and has the advantage of continuous operation, but the technology is not mature enough. The hydrate method is still in the laboratory. So developing a method of simple process, reliable performance, low energy consumption and low cost will be a research direction in the future.

Key words: enzymes, concentrate, separation, progress

摘要: 目前酶制剂生产过程中常用的浓缩方法存在工艺复杂、能耗较高、成本高昂等缺点, 并成为酶制剂工业进一步发展的关键步骤。本文综述了蒸发、超滤、吸附和冷冻等常用的酶制剂浓缩方法, 以及较新的离子液体和水合物浓缩酶制剂方法等, 并比较了这些方法的优缺点。蒸发浓缩酶制剂技术成熟, 但是能耗较高、酶失活率高。超滤和吸附浓缩酶制剂方法能耗较低, 但是膜和吸附材料成本较高、再生困难。冷冻酶制剂浓缩方法酶失活少, 但是浓缩率低。离子液体酶制剂浓缩方法具有保持酶活性、易于放大、可连续操作等优点, 但是技术仍不成熟。水合物酶制剂浓缩方法目前尚处于实验室研究阶段。因此, 开发出工艺简单、性能可靠、能耗较低、成本低廉的高纯度酶制剂浓缩方法依然是未来的研究方向。

关键词: 酶制剂, 浓缩, 分离, 进展

CLC Number: 

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