Nouri Marjan, Khodaiyan Faramarz
Bioprocessing and Biodetection Laboratory, Department of Food Science and Engineering, University of Tehran, Karaj, Iran.
Food Technol Biotechnol. 2020 Dec;58(4):391-401. doi: 10.17113/ftb.58.04.20.6737.
Pectinase enzyme has become a valuable compound in beverage industry. One of the most significant concepts to overcome the drawbacks of using industrial enzymes is their immobilization. In the present study, magnetic chitosan microparticles were utilized as a substrate for pectinase immobilization. New methods of enzyme immobilization involve the use of non-chemical cross-linkers between the enzyme and the substrate. The aim of this study is to immobilize the pectinase enzyme using polyaldehyde kefiran as a macromolecular cross-linker on magnetic particles.
Pectinase was immobilized in four steps: relative oxidation of kefiran and its application as a cross-linker, production of magnetic iron(II) iron(III) oxide (FeO) microparticles, coating of magnetic FeO microparticles with chitosan, and immobilization of the enzyme on the substrate, prepared by the use of oxidized kefiran cross-linker. Parameters such as cross-linking concentration, time and ratio of chitosan magnetic microparticles to enzyme were optimized. Fourier-transform infrared spectroscopy (FTIR), dynamic light scattering, transmission electron microscopy, and vibrating sample magnetometer were used to identify the groups and investigate the structures. The biochemical properties (stability of enzyme activity at different pH, temperature and time), enzyme reusability, kinetic parameters ( and ) and apple juice turbidity, using free and immobilized pectinase enzymes, were also measured.
Cross-linker concentration, cross-linking time and the ratio of magnetic FeO microparticles with chitosan to enzyme were important factors in activity recovery of pectinase. FTIR analysis correctly identified functional groups in the structures. The results showed that after enzyme stabilization, the particle size and molecular mass, respectively, increased and decreased the magnetic saturation strength. According to the thermal kinetic study, the activity of the immobilized pectinase was higher than of its free form. The findings of this study indicate excellent stability and durability of the immobilized pectinase. Finally, a magnetic pectinase micro-biocatalyst was used to clarify apple juice, which reduced turbidity during processing.
This study investigates the usage of kefiran oxidized as a new cross-linker for the immobilization of pectinase enzyme. Magnetic pectinase micro-biocatalyst has a good potential for industrial applications in the food industry, with high thermal stability.
果胶酶已成为饮料工业中的一种重要化合物。克服工业酶缺点的最重要概念之一是酶的固定化。在本研究中,磁性壳聚糖微粒被用作果胶酶固定化的载体。酶固定化的新方法涉及在酶和载体之间使用非化学交联剂。本研究的目的是使用聚醛基开菲尔多糖作为大分子交联剂在磁性颗粒上固定果胶酶。
果胶酶的固定化分四个步骤进行:开菲尔多糖的相对氧化及其作为交联剂的应用、磁性铁(II)铁(III)氧化物(FeO)微粒的制备、用壳聚糖包覆磁性FeO微粒以及通过使用氧化的开菲尔多糖交联剂将酶固定在载体上。对交联浓度、时间以及壳聚糖磁性微粒与酶的比例等参数进行了优化。使用傅里叶变换红外光谱(FTIR)、动态光散射、透射电子显微镜和振动样品磁强计来识别基团并研究结构。还测量了使用游离和固定化果胶酶时的生化特性(在不同pH、温度和时间下酶活性的稳定性)、酶的可重复使用性、动力学参数(米氏常数和最大反应速度)以及苹果汁的浊度。
交联剂浓度、交联时间以及磁性FeO微粒与壳聚糖的比例与酶的比例是影响果胶酶活性恢复的重要因素。FTIR分析正确识别了结构中的官能团。结果表明,酶稳定后,粒径和分子量分别增加和减小,磁饱和强度降低。根据热动力学研究,固定化果胶酶的活性高于游离形式。本研究结果表明固定化果胶酶具有出色的稳定性和耐久性。最后,使用磁性果胶酶微生物催化剂澄清苹果汁,降低了加工过程中的浊度。
本研究探讨了氧化开菲尔多糖作为果胶酶固定化新交联剂的用途。磁性果胶酶微生物催化剂在食品工业的工业应用中具有良好潜力,具有高热稳定性。