Engineering a highly active thermophilic beta-glucosidase to enhance its pH stability and saccharification performance

文献类型： 外文期刊

第一作者： Xia, Wei

作者： Xia, Wei;Shi, Pengjun;Bai, Yingguo;Luo, Huiying;Ma, Rui;Yao, Bin;Xia, Wei;Qian, Lichun;Xu, Xinxin

作者机构：

关键词： beta-Glucosidase;Talaromyce leycettanus;Saccharification;pH stability;O-glycosylation;Pichia pastoris

期刊名称：BIOTECHNOLOGY FOR BIOFUELS （ 影响因子：6.04； 五年影响因子：6.485 ）

ISSN： 1754-6834

年卷期： 2016 年 9 卷

页码：

收录情况： SCI

摘要： Background: beta-Glucosidase is an important member of the biomass-degrading enzyme system, and plays vital roles in enzymatic saccharification for biofuels production. Candidates with high activity and great stability over high temperature and varied pHs are always preferred in industrial practice. To achieve cost-effective biomass conversion, exploring natural enzymes, developing high level expression systems and engineering superior mutants are effective approaches commonly used. Results: A newly identified beta-glucosidase of GH3, Bgl3A, from Talaromyces leycettanus JCM12802, was overexpressed in yeast strain Pichia pastoris GS115, yielding a crude enzyme activity of 6000 U/ml in a 3 L fermentation tank. The purified enzyme exhibited outstanding enzymatic properties, including favorable temperature and pH optima (75 degrees C and pH 4.5), good thermostability (maintaining stable at 60 degrees C), and high catalytic performance (with a specific activity and catalytic efficiency of 905 U/mg and 9096/s/mM on pNPG, respectively). However, the narrow stability of Bgl3A at pH 4.0-5.0 would limit its industrial applications. Further site-directed mutagenesis indicated the role of excessive O-glycosylation in pH liability. By removing the potential O-glycosylation sites, two mutants showed improved pH stability over a broader pH range (3.0-10.0). Besides, with better stability under pH 5.0 and 50 degrees C compared with wild type Bgl3A, saccharification efficiency of mutant M1 was improved substantially cooperating with cellulase Celluclast 1.5L. And mutant M1 reached approximately equivalent saccharification performance to commercial beta-glucosidase Novozyme 188 with identical beta-glucosidase activity, suggesting its great prospect in biofuels production. Conclusions: In this study, we overexpressed a novel beta-glucosidase Bgl3A with high specific activity and high catalytic efficiency in P. pastoris. We further proved the negative effect of excessive O-glycosylation on the pH stability of Bgl3A, and enhanced the pH stability by reducing the O-glycosylation. And the enhanced mutants showed much better application prospect with substantially improved saccharification efficiency on cellulosic materials.

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