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胰蛋白酶的热响应性生物共轭物的制备与性质

Preparation and properties of thermoresponsive bioconjugates of trypsin.

作者信息

Raghava Smita, Mondal Kalyani, Gupta Munishwar N, Pareek Pradeep, Kuckling Dirk

机构信息

Chemistry Department, Indian Institute of Technology, Delhi, Hauz Khas, New Delhi, India.

出版信息

Artif Cells Blood Substit Immobil Biotechnol. 2006;34(3):323-36. doi: 10.1080/10731190600683902.

Abstract

Covalent attachment of enzymes and other proteins to the smart polymer, poly(N-isopropylacrylamide) [poly (NIPAAm)], has been widely used as a method for the preparation of thermosensitive protein conjugates. In the present study, reversible soluble-insoluble polymer-enzyme conjugates were prepared by conjugating a copolymer of NIPAAm with 5-mol % of 6-acrylaminohexanoic acid to trypsin by the carbodiimide-NHS (N-hydroxysuccinimide) coupling method. Four bioconjugates with different units of enzyme coupled to the matrix were prepared. Increased enzymatic activity in terms of high effectiveness factor (in the range of 3-5) was found in the conjugates. Kinetic parameters for the immobilized and free enzyme were determined. The Vmax/Km value of the enzyme significantly increased on immobilization by the factors in the range of 12-28. The immobilized enzyme also showed stability to autolysis at 50 degrees C.

摘要

将酶和其他蛋白质共价连接到智能聚合物聚(N-异丙基丙烯酰胺)[聚(NIPAAm)]上,已被广泛用作制备热敏蛋白缀合物的方法。在本研究中,通过碳二亚胺-NHS(N-羟基琥珀酰亚胺)偶联法,将含有5摩尔%6-丙烯酰胺基己酸的NIPAAm共聚物与胰蛋白酶偶联,制备了可逆的可溶-不溶性聚合物-酶缀合物。制备了四种不同酶单位与基质偶联的生物缀合物。在缀合物中发现以高效因子(3-5范围内)表示的酶活性增加。测定了固定化酶和游离酶的动力学参数。固定化后,酶的Vmax/Km值显著增加,增加因子在12-28范围内。固定化酶在50℃下也表现出对自溶的稳定性。

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