Department of Chemical Engineering, SSN College of Engineering, Kalavakkam, India.
Department of Petrochemical Engineering, SVS College of Engineering, Coimbatore, India.
Appl Biochem Biotechnol. 2018 Sep;186(1):174-185. doi: 10.1007/s12010-018-2719-1. Epub 2018 Mar 14.
Herein, the magnetite nanoparticles (MNs) were prepared by facile solvothermal method and its porous nature was modified using 3-(2-aminoethyl)-3-aminopropyl trimethoxysilane (AEAPS). Magnetite formation, successful amino tagging, and urease conjugation on the surface were confirmed from the presence of certain functional groups in Fourier transform infrared (FT-IR) spectra. Also, nanosize (13.2 nm) and spherical morphology of MNs were evaluated from diffraction patterns and electron micrographs respectively. Lower retentivity and coercivities in magnetization curve revealed the superparamagnetic behavior, and nitrogen adsorption/desorption curves exhibited decrease in its surface porosity. Conductivity measurements showed lower diffusion coefficient (D = 1.9 × 10 cm/min) and higher diffusion with limited hydrolytic reaction in native urease and improved activity of conjugated urease with higher D (12.62 × 10 cm/min). Hence, this study revealed that the surface porous nature of MNs can be altered effectively by amino tagging in order to overcome diffusional limitations thereby enhancing enzyme activity.
在此,通过简便的溶剂热法制备了磁铁矿纳米粒子(MNs),并使用 3-(2-氨乙基)-3-氨基丙基三甲氧基硅烷(AEAPS)对其多孔性质进行了修饰。从傅里叶变换红外(FT-IR)光谱中某些官能团的存在证实了磁铁矿的形成、成功的氨基标记和表面上的脲酶结合。此外,通过衍射图谱和电子显微镜图分别评估了 MNs 的纳米尺寸(13.2nm)和球形形态。磁化曲线中的较低保持力和矫顽力表明具有超顺磁性行为,并且氮气吸附/解吸曲线显示其表面孔隙率降低。电导率测量表明,天然脲酶的扩散系数(D=1.9×10cm/min)较低,且有限水解反应的扩散较高,而共轭脲酶的 D 值较高(12.62×10cm/min),活性也有所提高。因此,这项研究表明,通过氨基标记可以有效地改变 MNs 的表面多孔性质,从而克服扩散限制,提高酶的活性。