异质表达壳聚糖酶结合绿色球磨法进行酶降解

Haipeng Su, Jianan Sun, Chaoran Guo, Zhenrong Jia, Xiangzhao Mao
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引用次数: 3

摘要

壳寡糖(COSs)和d-氨基葡萄糖(GlcN)是具有多种生理功能的最有价值的生物分子,它们可以通过生物酶降解从壳聚糖中提取,而壳聚糖酶在这一过程中起着关键作用。另一方面,壳聚糖预处理是酶解生物生产的必要步骤。因此,绿色高效的预处理策略和优良的酶活性是实现规模化生产的关键。研究了球磨预处理的壳聚糖(PC)的环境友好高效酶解。首先,异源表达得到OUC-CsnPT,这是一种糖苷水解酶家族46壳聚糖酶,在pH 6.0°C和45°C下的优势比活性为5346.56 U/mg。内型壳聚糖酶OUC-CsnPT水解壳聚糖生成GlcN和壳聚糖[(GlcN)2]。然后,采用球磨法预处理PC,促进壳聚糖酶OUC-CsnPT水解,并通过扫描电镜、x射线衍射和ftir衰减全反射对其有效性进行表征。采用新工艺制备球磨壳聚糖,当球磨浓度为14.5 μmol/ml时,壳聚糖和GlcN的收率提高了10.8倍。因此,该技术为低聚糖生产提供了一种简单而环保的选择,拓宽了PC生物降解的理论基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Heterogenously-expressed chitosanase combining a green ball milling method for enzymatic degradation

Heterogenously-expressed chitosanase combining a green ball milling method for enzymatic degradation

Chitooligosaccharides (COSs) and d-glucosamine (GlcN), the most valuable biomolecules due to their various physiological functions, can be available inexpensively from chitosan by bio-enzymatic degradation, in which chitosanases play a key role. On the other hand, pretreatment of chitosan is the necessary procedure in the bioproduction by enzymatic hydrolysis. Therefore, the green and efficient pretreatment strategy as well as superior enzyme activity are the most critical aspects in scaled up production. This study investigated environmentally friendly and efficient enzymatic hydrolysis of powdery chitosan (PC) pretreated by ball-milling. First, heterologous expression yielded OUC-CsnPT, a glycoside hydrolase family 46 chitosanase with a predominant specific activity of 5346.56 U/mg at pH 6.0°C and 45°C. The endo-type chitosanase OUC-CsnPT hydrolyzed chitosan to produce GlcN and chitobiose [(GlcN)2]. Then, ball-milling was employed to pretreat PC to promote chitosanase OUC-CsnPT hydrolysis, and the effectiveness was characterized by scanning electron microscope, X-ray diffraction, and FTIR-attenuated total reflection. Through the development of the novel route, the yield of COSs and GlcN for ball-milling powdery chitosan increased by 10.8-folds with a concentration of 14.5 μmol/ml. Hence, this technique presents a promising strategy suited to be a straightforward and environmentally friendly option for oligosaccharides production, broadening the theoretical basis for PC biodegradation.

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