EXPRESSION AND PURIFICATION OF PHYTOPHTHORA INFESTANS (MONT.) DE. BRAY RXLR EFFECTOR

被引:0
|
作者
Yu, Ping
Dong, Chao
Yao, Chunxin
Zhou, Xiaogang [1 ]
Ding, Yumei
机构
[1] Yunnan Acad Agr Sci, Biotechnol & Germplasm Resources Inst, Kunming 650205, Yunnan, Peoples R China
来源
BANGLADESH JOURNAL OF BOTANY | 2019年 / 48卷 / 03期
关键词
Effector protein; Gene cloning; Prokaryotic expression; Protein purification;
D O I
暂无
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The RXLR-class effectors play an important role in the pathogenesis of pathogens. They not only can enhance the pathogenicity of the pathogen, but also can be identified as a non-toxic protein to induce cell hypersensitive response (HR) by resistance protein of the host plant. In this study, the gene of RXLR effector was amplified by PCR, then the target gene and expression vector pET-28a were ligated and transformed into BL21( DE3) competent cells to obtain the pET-28a-RXLR recombinant expression plasmid. The protein was induced expressed by IPTG, purified by Ni affinity chromatography and detected by SDS-PAGE. The recombinant expression plasmid pET-28a-RXLR was successfully constructed and expressed in E. coli to produce a protein sized 18.4 kDa, consistent with the theoretical value. The high purity RXLR effector was successfully obtained in this study, laying a foundation for its pathogenicity study.
引用
收藏
页码:783 / 787
页数:5
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