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胃蛋白酶对壳聚糖酶解的优化与表征

Optimization and Characterization of Chitosan Enzymolysis by Pepsin.

作者信息

Gohi Bi Foua Claude Alain, Zeng Hong-Yan, Pan A Dan

机构信息

Biotechnology Institute, College of Chemical Engineering, Xiangtan University, Xiangtan 411105, Hunan, China.

出版信息

Bioengineering (Basel). 2016 Jul 1;3(3):17. doi: 10.3390/bioengineering3030017.

Abstract

Pepsin was used to effectively degrade chitosan in order to make it more useful in biotechnological applications. The optimal conditions of enzymolysis were investigated on the basis of the response surface methodology (RSM). The structure of the degraded product was characterized by degree of depolymerization (DD), viscosity, molecular weight, FTIR, UV-VIS, SEM and polydispersity index analyses. The mechanism of chitosan degradation was correlated with cleavage of the glycosidic bond, whereby the chain of chitosan macromolecules was broken into smaller units, resulting in decreasing viscosity. The enzymolysis by pepsin was therefore a potentially applicable technique for the production of low molecular chitosan. Additionally, the substrate degradation kinetics of chitosan were also studied over a range of initial chitosan concentrations (3.0~18.0 g/L) in order to study the characteristics of chitosan degradation. The dependence of the rate of chitosan degradation on the concentration of the chitosan can be described by Haldane's model. In this model, the initial chitosan concentration above which the pepsin undergoes inhibition is inferred theoretically to be about 10.5 g/L.

摘要

胃蛋白酶被用于有效降解壳聚糖,以便使其在生物技术应用中更有用。基于响应面法(RSM)研究了酶解的最佳条件。通过解聚度(DD)、粘度、分子量、傅里叶变换红外光谱(FTIR)、紫外可见光谱(UV-VIS)、扫描电子显微镜(SEM)和多分散指数分析对降解产物的结构进行了表征。壳聚糖降解的机制与糖苷键的断裂相关,由此壳聚糖大分子链被分解成较小的单元,导致粘度降低。因此,胃蛋白酶酶解是一种生产低分子壳聚糖的潜在适用技术。此外,还研究了在一系列初始壳聚糖浓度(3.0~18.0 g/L)范围内壳聚糖的底物降解动力学,以研究壳聚糖降解的特性。壳聚糖降解速率对壳聚糖浓度的依赖性可用哈尔丹模型描述。在该模型中,理论上推断胃蛋白酶受到抑制时的初始壳聚糖浓度约为10.5 g/L。

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