Liu Li, Sun Yunhui, He Lilu, Jiang Linlin, Yang Sen
College of Resources and Environmental Sciences, China Agricultural University, Beijing 100193, PR China.
College of Resources and Environmental Sciences, China Agricultural University, Beijing 100193, PR China.
Enzyme Microb Technol. 2015 Nov;79-80:19-26. doi: 10.1016/j.enzmictec.2015.06.015. Epub 2015 Jul 4.
This study reports a general strategy for the encapsulation of various enzymes in amphiphilic hollow carbonaceous microspheres (CMs). We found that enzymes could be spontaneously encapsulated in the interior cavity of the CMs via hydrophobic interactions. Due to strong hydrophobic interactions and robust confinement, leaching of the physically adsorbed enzymes is substantially restricted. As a novel immobilization matrix, the CMs display many significant advantages. They are capable of encapsulating a wide range of proteins/enzymes of different sizes, which can then be used in both aqueous and organic media and retain high activity, stability, and excellent reusability. Moreover, CMs could be considered as efficient microreactors that provide a favorable microaqueous environment for enzymes in organic systems. Therefore, this doubly effective and simple immobilization approach can be easily expanded to many other enzymes and has great potential in a variety of enzyme applications.
本研究报道了一种将各种酶封装在两亲性空心碳质微球(CMs)中的通用策略。我们发现,酶可通过疏水相互作用自发封装在CMs的内腔中。由于强烈的疏水相互作用和强大的限制作用,物理吸附酶的浸出受到显著限制。作为一种新型固定化基质,CMs具有许多显著优点。它们能够封装各种不同大小的蛋白质/酶,这些蛋白质/酶随后可在水性和有机介质中使用,并保持高活性、稳定性和出色的可重复使用性。此外,CMs可被视为高效的微反应器,为有机体系中的酶提供有利的微水环境。因此,这种双重有效且简单的固定化方法可轻松扩展到许多其他酶,在各种酶应用中具有巨大潜力。