| Literature DB >> 26920265 |
Jie Long1, Enbo Xu1, Xingfei Li1, Zhengzong Wu1, Fang Wang1, Xueming Xu1, Zhengyu Jin2, Aiquan Jiao3, Xiaobei Zhan4.
Abstract
The interactions between pullulanase and chitosans of different molecular weights (Mw) were comprehensively studied, and their applications in pullulanase immobilization onto Fe3O4-κ-carrageenan nanoparticles upon chitosan-pullulanase complexation were also evaluated. Chitosan (CS) complexation with pullulanase was found to be dependent on pH and chitosan Mw. The critical pH of structure-forming events during complexation shifted significantly (p<0.05) to a lower pH with a low Mw chitosan (50kDa) compared to other chitosan types. Binding constants for the chitosan-pullulanase interaction increased in the following order: CS-500<CS-400<CS-50<CS-200. The binding induced alterations in the protein secondary structure, which may affect the enzymatic properties of immobilized pullulanase. Pullulanase immobilized upon CS-50 complexation exhibited the most desirable enzymatic properties. These results indicated that the complexation behavior was mainly dependent on chitosan Mw. This study presents a technique for the production of immobilized pullulanase upon complexation that exhibits potential for applications in continuous syrup production. CrownEntities:
Keywords: Chitosan; Complex; Fe(3)O(4)–κ-carrageenan nanoparticles; Molecular weight; Pullulanase
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Year: 2016 PMID: 26920265 DOI: 10.1016/j.foodchem.2016.01.119
Source DB: PubMed Journal: Food Chem ISSN: 0308-8146 Impact factor: 7.514