Lin Nay San, Hirayama Kota, Kitamura Masaki, Koide Shinji, Kitajima Hiromasa, Harada Takunori, Mayama Shigeki, Umemura Kazuo
Department of Physics, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku, Tokyo 1628601, Japan.
Department of Integrated Science and Technology, Faculty of Science and Technology, Oita University, Dannoharu, 700, Oita City 870-1192, Japan.
ACS Omega. 2023 May 27;8(23):21145-21153. doi: 10.1021/acsomega.3c02104. eCollection 2023 Jun 13.
Immobilization of enzymes has been widely reported due to their reusability, thermal stability, better storage abilities, and so on. However, there are still problems that immobilized enzymes do not have free movements to react to substrates during enzyme reactions and their enzyme activity becomes weak. Moreover, when only the porosity of support materials is focused, some problems such as enzyme distortion can negatively affect the enzyme activity. Being a solution to these problems, a new function "floatability" of enzyme devices has been discussed. A "floatable" micron-sized enzyme device was fabricated to enhance the free movements of immobilized enzymes. Diatom frustules, natural nanoporous biosilica, were used to attach papain enzyme molecules. The floatability of the frustules, evaluated by macroscopic and microscopic methods, was significantly better than that of four other SiO materials, such as diatomaceous earth (DE), which have been widely used to fabricate micron-sized enzyme devices. The frustules were fully suspended at 30 °C for 1 h without stirring, although they settled at room temperature. When enzyme assays were performed at room temperature, 37, and 60 °C with or without external stirring, the proposed frustule device showed the highest enzyme activity under all conditions among papain devices similarly prepared using other SiO materials. It was confirmed by the free papain experiments that the frustule device was active enough for enzyme reactions. Our data indicated that the high floatability of the reusable frustule device, and its large surface area, is effective in maximizing enzyme activity due to the high probability to react to substrates.
由于酶的可重复使用性、热稳定性、更好的储存能力等,酶的固定化已被广泛报道。然而,仍然存在一些问题,即固定化酶在酶促反应过程中没有自由移动来与底物反应,并且它们的酶活性会变弱。此外,当仅关注载体材料的孔隙率时,一些问题如酶的变形会对酶活性产生负面影响。作为解决这些问题的方法,人们讨论了酶装置的一种新功能“漂浮性”。制备了一种“可漂浮”的微米级酶装置,以增强固定化酶的自由移动。硅藻壳,即天然纳米多孔生物二氧化硅,被用于附着木瓜蛋白酶分子。通过宏观和微观方法评估,硅藻壳的漂浮性明显优于其他四种常用于制造微米级酶装置的SiO材料,如硅藻土(DE)。尽管硅藻壳在室温下会沉降,但在30°C下不搅拌时它们能完全悬浮1小时。当在室温、37°C和60°C下进行酶活性测定时,无论有无外部搅拌,所提出的硅藻壳装置在使用其他SiO材料类似制备的木瓜蛋白酶装置中,在所有条件下都显示出最高的酶活性。通过游离木瓜蛋白酶实验证实,硅藻壳装置对酶促反应具有足够的活性。我们的数据表明,可重复使用的硅藻壳装置的高漂浮性及其大表面积,由于与底物反应的概率高,有效地最大化了酶活性。