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游离及固定化泡盛曲霉淀粉酶的生产、固定化及热力学研究

Production, immobilization and thermodynamic studies of free and immobilized Aspergillus awamori amylase.

作者信息

Karam Eman A, Abdel Wahab Walaa A, Saleh Shireen A A, Hassan Mohamed E, Kansoh Amany L, Esawy Mona A

机构信息

Microbial Chemistry Department, National Research Centre, Dokki, Cairo,, Egypt.

Department of Chemistry of Natural and Microbial Products, National Research Centre, Dokki, Cairo, Egypt.

出版信息

Int J Biol Macromol. 2017 Sep;102:694-703. doi: 10.1016/j.ijbiomac.2017.04.033. Epub 2017 Apr 21.

Abstract

Enzyme cost, stability and its thermodynamic characteristics are the main criteria for industrial use. In this study, Aspergillus awamori amylase was constitutively produced using various agro-industrial wastes. Olive oil cake gave the highest activity (230U/g). The amylase was partially purified to 2.81-fold purification. Immobilization was achieved using different carriers by covalent binding. The novel carrier Ca alginate (Alg) starch (St)/polyethyleneimine (PEI)/glutaraldehyde (GA), showed the highest operational stability and was selected for further studies. The optimum temperature for the free and immobilized form was 50°C and 55-60°C, respectively. The immobilization process had a major role in improving enzyme thermal stability. In comparison to free enzyme, the immobilized form showed the highest optimum temperature, activation energy (E) and deactivation rate constants (k). Also, t, D-values (decimal reduction time), change in enthalpy (ΔH° kJmol), and Gibbs free energy (ΔG°) increased and was higher than the native enzyme within 50-80°C. The magnitude of negative value of entropy (ΔS° kJmol) for immobilized enzyme was negative for the free and immobilized enzymes revealing that native form of enzyme was in more ordered state. K and V values were slightly affected by the temperature variations 40-70°C.

摘要

酶的成本、稳定性及其热力学特性是工业应用的主要标准。在本研究中,使用各种农业工业废弃物组成型生产泡盛曲霉淀粉酶。橄榄油饼产生的活性最高(230U/g)。该淀粉酶被部分纯化至2.81倍的纯化倍数。通过共价结合使用不同载体实现固定化。新型载体海藻酸钙(Alg)淀粉(St)/聚乙烯亚胺(PEI)/戊二醛(GA)表现出最高的操作稳定性,并被选用于进一步研究。游离酶和固定化酶的最适温度分别为50°C和55 - 60°C。固定化过程在提高酶的热稳定性方面起主要作用。与游离酶相比,固定化酶表现出最高的最适温度、活化能(E)和失活速率常数(k)。此外,在50 - 80°C范围内,t、D值(十进制减少时间)、焓变(ΔH°kJmol)和吉布斯自由能(ΔG°)增加且高于天然酶。固定化酶的熵负值(ΔS°kJmol)的大小对于游离酶和固定化酶均为负值,这表明酶的天然形式处于更有序的状态。K和V值在40 - 70°C的温度变化下受到轻微影响。

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