Department of Biological Applications and Technologies, University of Ioannina, Ioannina, Greece.
Bioresour Technol. 2012 Jul;115:164-71. doi: 10.1016/j.biortech.2011.11.007. Epub 2011 Nov 10.
In this study we report the use of functionalized carbon-based nanomaterials, such as amine-functionalized graphene oxide (GO) and multi-walled carbon nanotubes (CNTs), as effective immobilization supports for various lipases and esterases of industrial interest. Structural and biochemical characterization have revealed that the curvature of the nanomaterial affect the immobilization yield, the catalytic behavior and the secondary structure of enzymes. Infrared spectroscopy study indicates that the catalytic behavior of the immobilized enzymes is correlated with their α-helical content. Hydrolases exhibit higher esterification activity (up to 20-fold) when immobilized on CNTs compared to GO. The covalently immobilized enzymes exhibited comparable or even higher activity compared to the physically adsorbed ones, while they presented higher operational stability. The enhanced catalytic behavior observed for most of the hydrolases covalently immobilized on amine-functionalized CNTs indicate that these functionalized nanomaterials are suitable for the development of efficient nanobiocatalytic systems.
在这项研究中,我们报告了功能化碳基纳米材料(如胺功能化氧化石墨烯(GO)和多壁碳纳米管(CNT))作为各种具有工业应用价值的脂肪酶和酯酶的有效固定化载体的用途。结构和生化特性研究表明,纳米材料的曲率会影响酶的固定化产率、催化行为和二级结构。红外光谱研究表明,固定化酶的催化行为与其α-螺旋含量有关。与 GO 相比,固定在 CNTs 上的水解酶具有更高的酯化活性(高达 20 倍)。与物理吸附的酶相比,共价固定化的酶表现出相当或更高的活性,同时具有更高的操作稳定性。大多数共价固定在胺功能化 CNTs 上的水解酶表现出增强的催化行为,这表明这些功能化纳米材料适合开发高效的纳米生物催化系统。