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Integrated Strategies for Enhancing the Expression of the AqCoA Chitosanase in Pichia pastoris by Combined Optimization of Molecular Chaperones Combinations and Copy Numbers via a Novel Plasmid pMC-GAP

文献类型： 外文期刊

作者： Wang, Yanxin 1 ; Luo, Xue 1 ; Zhao, Yuqiang 1 ; Ye, Xianfeng 1 ; Yang, Fan 1 ; Li, Zhoukun 1 ; Huang, Yan 1 ; Fang, Xiaod 1 ;

作者机构： 1.Nanjing Agr Univ, Minist Agr & Rural Affairs, Coll Life Sci, Key Lab Agr Environm Microbiol, Nanjing 210095, Peoples R China

2.Inst Bot, Nanjing 210014, Jiangsu, Peoples R China

3.Chinese Acad Sci, Nanjing Bot Garden Mem Sun Yat Sen, Nanjing 210014, Jiangsu, Peoples R China

4.Guangzhou Hanyun Parmaceut Technol Co Ltd, Guangzhou 510000, Peoples R China

5.Microbial Res Inst Liaoning Prov, Chaoyang, Peoples R China

6.Jiangsu Acad Agr Sci, Inst Vet Immunol & Engn, Nanjing 210014, Peoples R China

7.Nanjing Agr Univ, Key Lab Plant Immun, Nanjing 210095, Peoples R China

关键词： Chitosanase; Plasmid; Improvement; Gene copy; Molecular chaperones; Pichia pastoris

期刊名称：APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY （ 影响因子：2.926； 五年影响因子：2.685 ）

ISSN： 0273-2289

年卷期： 2021 年 193 卷 12 期

页码：

收录情况： SCI

摘要： In our previous study, the chitosanase AqCoA and the chitooligosaccharides it produced were found to exhibit significant protective effects against fungal diseases. In this study, we enhanced the expression of AqCoA using the novel pMC-GAP that enables stable transformation of Escherichia coli, and built an integrated model based on the gene copy number, molecular chaperones, and protein production of AqCoA. In terms of gene dosage, the highest hydrolase activity was 0.32 U/ml in the strain with four copies, which was 1.78-fold higher than that of the strain with only one copy (0.18 U/ml). In addition, we found the chaperones such as PDI, ERO1, HAC1, YDJ1, SSE1, SSA4, and SSO2 improved protein expression. Furthermore, the PDI/ERO1, SSA4/SSE1, and YDJ1/SSO2 pairs synergistically increased the expression levels by 61%, 31%, and 42%, respectively. Finally, we investigated the combined effects of gene copy numbers and molecular chaperones on protein expression. The highest activity reached 2.32 U/ml in the strain with six integrated molecular chaperone expression cassettes and sixteen copies of the target gene, which was 13-fold higher than that of the control strain with only one copy (GAP-1AqCoA). Combined optimization of gene dosage and molecular chaperone combinations significantly increased the expression level of AqCoA, providing a powerful strategy to improve the expression of other heterologous proteins in P. pastoris.

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