National Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China.
J Biotechnol. 2013 Oct 20;168(2):212-7. doi: 10.1016/j.jbiotec.2013.05.016. Epub 2013 Jun 10.
Efficient dynamic interactions among cofactor, enzymes and substrate molecules are of primary importance for multi-step enzymatic reactions with in situ cofactor regeneration. Here we showed for the first time that the above dynamic interactions could be significantly intensified by exerting an external alternating magnetic field on magnetic nanoparticles-supported multi-enzymatic system so that the inter-particle collisions due to Brownian motion of nanoparticles could be improved. To that end, a multienzyme system including glutamate dehydrogenase (GluDH), glucose dehydrogenase (GDH) and cofactor NAD(H) were separately immobilized on silica coated Fe3O4 magnetic nanoparticles with an average diameter of 105 nm, and the effect of magnetic field strength and frequency on the kinetics of the coupled bi-enzyme reaction was investigated. It was found that at low magnetic field frequency (25 Hz and 100 Hz), increasing magnetic field strength from 9.8 to 161.1 Gs led to only very slight increase in reaction rate of the coupled bi-enzyme reaction expressed by glucose consumption rate. At higher magnetic field of 200 Hz and 500 Hz, reaction rate increased significantly with increase of magnetic field strength. When the magnetic field frequency was kept at 500 Hz, the reaction rate increased from 3.89 μM/min to 8.11 μM/min by increasing magnetic field strength from 1.3 to 14.2 Gs. The immobilized bi-enzyme system also showed good reusability and stability in the magnetic field (500 Hz, 14.2 Gs), that about 46% of original activity could be retained after 33 repeated uses, accounting for totally 34 days continuous operation. These results demonstrated the feasibility in intensifying molecular interactions among magnetic nanoparticle-supported multienzymes by using nano-magnetic stirrer for efficient multi-step transformations.
在原位再生辅助因子的多步酶反应中,辅助因子、酶和底物分子之间的有效动态相互作用至关重要。在这里,我们首次表明,通过对外加交变磁场施加于磁性纳米粒子支撑的多酶系统,可以显著增强上述动态相互作用,从而提高由于纳米粒子的布朗运动引起的粒子间碰撞。为此,将包括谷氨酸脱氢酶 (GluDH)、葡萄糖脱氢酶 (GDH) 和辅助因子 NAD(H) 在内的多酶系统分别固定在平均直径为 105nm 的二氧化硅包覆的 Fe3O4 磁性纳米粒子上,并研究了磁场强度和频率对偶联双酶反应动力学的影响。结果发现,在低磁场频率 (25Hz 和 100Hz) 下,将磁场强度从 9.8 增加到 161.1Gs 仅导致葡萄糖消耗率表示的偶联双酶反应的反应速率略有增加。在更高的磁场 200Hz 和 500Hz 下,随着磁场强度的增加,反应速率显著增加。当磁场频率保持在 500Hz 时,通过将磁场强度从 1.3 增加到 14.2Gs,反应速率从 3.89μM/min 增加到 8.11μM/min。固定化双酶系统在磁场 (500Hz,14.2Gs) 中也表现出良好的可重复使用性和稳定性,经过 33 次重复使用后,仍保留约 46%的原始活性,相当于连续运行 34 天。这些结果表明,通过使用纳米磁搅拌器有效地强化磁性纳米粒子支撑的多酶之间的分子相互作用,从而实现多步转化的可行性。