Institute of Chemical Technology and Engineering, Faculty of Chemical Technology, Poznan University of Technology, Berdychowo 4, 60-965, Poznan, Poland.
Institute of Molecular Physics Polish Academy of Sciences, M. Smoluchowskiego 17, 60-179, Poznan, Poland.
Sci Rep. 2022 May 4;12(1):7218. doi: 10.1038/s41598-022-11319-0.
In this work, new MO/fucoidan hybrid systems were fabricated and applied in lipase immobilization. Magnesium (MgO) and zirconium (ZrO) oxides were used as MO inorganic matrices. In the first step, the proposed oxides were functionalized with fucoidan from Fucus vesiculosus (Fuc). The obtained MgO/Fuc and ZrO/Fuc hybrids were characterized by means of spectroscopic analyses, including Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and nuclear magnetic resonance. Additionally, thermogravimetric analysis was performed to determine the thermal stability of the hybrids. Based on the results, the mechanism of interaction between the oxide supports and fucoidan was also determined. Furthermore, the fabricated MO/fucoidan hybrid materials were used as supports for the immobilization of lipase from Aspergillus niger, and a model reaction (transformation of p-nitrophenyl palmitate to p-nitrophenol) was performed to determine the catalytic activity of the proposed biocatalytic system. In that reaction, the immobilized lipase exhibited high apparent and specific activity (145.5 U/g and 1.58 U/mg for lipase immobilized on MgO/Fuc; 144.0 U/g and 2.03 U/mg for lipase immobilized on ZrO/Fuc). The immobilization efficiency was also confirmed using spectroscopic analyses (FTIR and XPS) and confocal microscopy.
在这项工作中,制备了新型 MO/褐藻糖胶杂化体系,并将其应用于脂肪酶固定化。使用氧化镁(MgO)和氧化锆(ZrO)作为 MO 无机基质。在第一步中,用来自泡叶藻(Fucus vesiculosus)的褐藻糖胶(Fuc)对所提出的氧化物进行功能化。通过光谱分析,包括傅里叶变换红外光谱、X 射线光电子能谱和核磁共振,对获得的 MgO/Fuc 和 ZrO/Fuc 杂化物进行了表征。此外,还进行了热重分析以确定杂化物的热稳定性。基于这些结果,还确定了氧化物载体与褐藻糖胶之间的相互作用机制。此外,所制备的 MO/褐藻糖胶杂化材料被用作固定化黑曲霉脂肪酶的载体,并进行了模型反应(棕榈酸对硝基苯酯转化为对硝基苯酚)以确定所提出的生物催化体系的催化活性。在该反应中,固定化脂肪酶表现出高的表观和比活性(MgO/Fuc 上固定化的脂肪酶为 145.5 U/g 和 1.58 U/mg;ZrO/Fuc 上固定化的脂肪酶为 144.0 U/g 和 2.03 U/mg)。还通过光谱分析(FTIR 和 XPS)和共聚焦显微镜证实了固定化效率。