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2025年8月14日 星期四
农业生物技术学报  2022, Vol. 30 Issue (11): 2246-2254    DOI: 10.3969/j.issn.1674-7968.2022.11.017
  研究资源与技术改进 本期目录 | 过刊浏览 | 高级检索 |
FpgMBV1-P4基因的原核表达及多克隆抗体制备
刘东伟1, 宋嘉庆1, 潘鑫1, 闫书味1, 李轲1, 范沛3, 高飞1, 张晓婷1,*, 代君丽1,*, 李洪连1,2
1 河南农业大学 植物保护学院,郑州450002;
2 小麦玉米作物学国家重点实验室,郑州 450046;
3 河南工业大学 生物工程学院,郑州 450001
Prokaryotic Expression of FpgMBV1-P4 Gene and Preparation of Its Polyclonal Antibodies
LIU Dong-Wei1, SONG Jia-Qing1, PAN Xin1, YAN Shu-Wei1, LI Ke1, FAN Pei3, GAO Fei1, ZHANG Xiao-Ting1,*, DAI Jun-Li1,*, LI Hong-Lian1,2
1 College of Plant Protection, Henan Agricultural University, Zhengzhou 450002, China;
2 State Key Laboratory of Wheat and Maize Crop Science, Zhengzhou 450046, China;
3 Colledge of Biology Engineering, Henan University of Technology, Zhengzhou 450001, China
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摘要 假禾谷镰孢巨型双链RNA病毒1 (Fusarium pseudograminearum megabirnavirus 1, FpgMBV1)是从假禾谷镰孢(Fusarium pseudograminearum)弱毒菌株FC136-2A中发现的一种真菌病毒。FpgMBV1共编码4个蛋白质,其中FpgMBV1-P4由268个氨基酸残基组成,功能未知。本研究设计特异性引物,采用反转录PCR (reverse transcription PCR, RT-PCR)方法从菌株FC136-2A的菌丝中扩增FpgMBV1-P4基因,构建原核表达载体pGEX4T-FpgMBV1-P4并转化大肠杆菌(Escherichia coli) BL21(DE3)菌株,在25 ℃以0.5 mmol/L异丙基硫代半乳糖苷(isopropyl β-D-thiogalactoside, IPTG)诱导表达重组蛋白。结果表明,FpgMBV1-P4基因长为807 bp,重组表达的融合蛋白分子量约为60 kD,与预期大小相符。将该重组蛋白作为抗原免疫新西兰大白兔(Lepus sinensis),获得抗血清,采用间接ELISA测定其效价达1∶160 000,能够特异性检测到假禾谷镰孢菌丝中约36 kD的FpgMBV1-P4蛋白。研究结果为深入分析FpgMBV1-P4的结构和功能及进一步探讨FpgMBV1与假禾谷镰孢菌的相互作用提供了基础。
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刘东伟
宋嘉庆
潘鑫
闫书味
李轲
范沛
高飞
张晓婷
代君丽
李洪连
关键词 真菌病毒假禾谷镰孢巨型双链RNA病毒1 (FpgMBV1)P4蛋白原核表达多克隆抗体    
AbstractFusarium pseudograminearum megabirnavirus 1 (FpgMBV1) is a mycovirus found in the hypovirulence Fusarium pseudograminearum strain FC136-2A. Four proteins were encoded in FpgMBV1. Among them, FpgMBV1-P4 composed of 268 amino acids with unknown function. Specific primers were designed and used in reverse transcription PCR (RT-PCR) to amplify the FpgMBV1-P4 gene from the hyphae of the strain FC136-2A in this study. Then a prokaryotic expression vector pGEX4T-FpgMBV1-P4 was constructed and transformed into Escherichia coli BL21(DE3) strain, and the recombinant protein was induced at 25 ℃ with 0.5 mmol/L isopropyl β-D-thiogalactoside (IPTG). Results showed that FpgMBV1-P4 in length of 807 bp was successfully amplified and the fusion protein with a molecular weight of about 60 kD was highly expressed . The purified fusion protein was used to immunize Zealand white rabbit (Lepus sinensis) to obtain antiserum. Indirect ELISA results showed the titer of this antiserum reached 1∶160 000. And the antiserum was used to specifically detect the FpgMBV1-P4 protein at about 36 kD from samples of the hyphae of FC136-2A. These results laid a foundation for the structural and functional analysis of FpgMBV1-P4, which would be meaningful in deciphering the hypovirulent mechanism of FpgMBV1.
Key wordsMycovirus    Fusarium pseudograminearum megabirnavirus 1 (FpgMBV1)    P4 protein    Prokaryotic expression    Polyclonal antibody
收稿日期: 2021-11-24     
ZTFLH:  S432.1  
基金资助:国家自然科学基金国际(地区)合作与交流项目(31961143018); 河南省科技攻关计划(农业领域)项目(212102110138); 2018年度河南省高等学校青年骨干教师培养计划(2018GGJS032); 河南农业大学科技创新基金(KJCX2020A14)
通讯作者: * zhangxiaoting921@163.com;daij666@126.com   
引用本文:   
刘东伟, 宋嘉庆, 潘鑫, 闫书味, 李轲, 范沛, 高飞, 张晓婷, 代君丽, 李洪连. FpgMBV1-P4基因的原核表达及多克隆抗体制备[J]. 农业生物技术学报, 2022, 30(11): 2246-2254.
LIU Dong-Wei, SONG Jia-Qing, PAN Xin, YAN Shu-Wei, LI Ke, FAN Pei, GAO Fei, ZHANG Xiao-Ting, DAI Jun-Li, LI Hong-Lian. Prokaryotic Expression of FpgMBV1-P4 Gene and Preparation of Its Polyclonal Antibodies. 农业生物技术学报, 2022, 30(11): 2246-2254.
链接本文:  
http://journal05.magtech.org.cn/Jwk_ny/CN/10.3969/j.issn.1674-7968.2022.11.017     或     http://journal05.magtech.org.cn/Jwk_ny/CN/Y2022/V30/I11/2246
 
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