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2025年7月29日 星期二
农业生物技术学报  2019, Vol. 27 Issue (2): 315-322    DOI: 10.3969/j.issn.1674-7968.2019.02.014
  研究论文与报告 本期目录 | 过刊浏览 | 高级检索 |
苹果树腐烂病菌木聚糖酶VmXyl1基因的原核表达及多克隆抗体制备
孟璐璐*, 于春蕾*, 练森, 李保华, 梁文星, 王彩霞*
青岛农业大学 植物医学学院/山东省植物病虫害综合防控重点实验室/山东省应用真菌重点实验室,青岛 266109
Prokaryotic Expression of Xylanase VmXyl1 Gene in Valsa mali and Preparation of Polyclonal Antibody
MENG Lu-Lu*, YU Chun-Lei*, LIAN Sen, LI Bao-Hua, LIANG Wen-Xing, WANG Cai-Xia**
College of Plant Health and Medicine, Key Laboratory of Integrated Crop Pest Management of Shandong, Shandong Province Key Laboratory of Applied Mycology, Qingdao Agricultural University, Qingdao 266109, China
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摘要 木聚糖酶(xylanase)基因VmXyl1在苹果树腐烂病菌—黑腐皮壳菌(Valsa mali)致病过程中发挥重要作用。为了揭示VmXyl1在腐烂病菌与寄主互作过程中的作用机制,本研究构建了原核表达载体pET-32a-VmXyl1,利用异丙基-β-D-硫代半乳糖苷(isopropyl β-D-1-thiogalactopyranoside, IPTG)进行诱导,在大肠杆菌(Escherichia coli)表达菌株Rosetta (DE3)中成功表达了VmXyl1融合蛋白;利用十二烷基硫酸钠聚丙烯酰胺凝胶电泳(sodium dodecyl sulfate polyacrylamide gel electrophoresis, SDS-PAGE)检测融合蛋白的可溶性和纯化效果,免疫新西兰白兔(Oryctolagus cuniculus)制备多克隆抗体,并对其效价和特异性进行分析。结果显示,该蛋白主要以包涵体形式存在,且0.5 mmol/L IPTG、30 ℃诱导8 h融合蛋白高效表达;经Ni-NTA柱亲和层析纯化后,获得了预期大小的融合蛋白。酶联免疫吸附测定(enzyme-linked immunosorbent assay, ELISA)和Western blot分析表明,所制备抗体效价达1∶102 400,且抗体能特异性识别VmXyl1融合蛋白及发病苹果(Malus pumila)树皮组织中的木聚糖酶蛋白,说明所制备的抗体具有高效性和特异性。研究结果为深入探究腐烂病菌木聚糖酶的致病机理及其与寄主的互作机制提供了基础资料。
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孟璐璐
于春蕾
练森
李保华
梁文星
王彩霞
关键词 苹果树腐烂病菌木聚糖酶基因原核表达多克隆抗体    
Abstract:Xylanase VmXyl1 plays an important role in the pathogenesis of Valsa mali. In order to reveal the action mechanism of VmXyl1 in the interaction of V. mali and host, a recombinant plasmid pET-32a-VmXyl1 was constructed in this study. The fusion protein VmXyl1 was expressed successfully in Escherichia coli Rosetta (DE3) strain when induced by isopropyl β-D-1-thiogalactopyranoside (IPTG). The solubility and purification effects of the fusion protein were detected by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). Then, New Zealand white rabbits (Oryctolagus cuniculus) were immunized with purified VmXyl1 protein and polyclonal antibody was prepared. The titer and specificity of the antibody were analyzed by enzyme-linked immunosorbent assay (ELISA) and Western blot. The sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) results showed that the fusion protein VmXyl1 mainly existed in the form of inclusion body, and the protein was expressed abundantly under induction by 0.5 mmol/L IPTG for 8 h at 30 ℃. The target protein with high purity was obtained by the Ni-NTA affinity chromatography. ELISA showed that the titer of prepared antibody was up to 1∶102 400. Western blot analysis demonstrated the polyclonal antibody could specifically recognize both the fusion protein VmXyl1 and xylanase protein in the apple (Malus pumila) bark tissue infected by V. mali, which indicated that the prepared antibody had high efficiency and specificity. The results in this study provide basic data for further exploring the pathogenesis of V. mali xylanase and its interaction mechanism with the host.
Key wordsValsa mali    Xylanase gene    Prokaryotic expression    Polyclonal antibody
收稿日期: 2018-08-03     
ZTFLH:  S436.611.11  
基金资助:山东省自然科学基金(No.ZR2018MC020)、国家自然科学基金(No.31272001和No.31371883)、青岛农业大学研究生创新立项(No.QYC201716)和山东省“泰山学者”建设工程专项
通讯作者: **,cxwang@qau.edu.cn。   
作者简介: *同等贡献作者。
引用本文:   
孟璐璐, 于春蕾, 练森, 李保华, 梁文星, 王彩霞. 苹果树腐烂病菌木聚糖酶VmXyl1基因的原核表达及多克隆抗体制备[J]. 农业生物技术学报, 2019, 27(2): 315-322.
MENG Lu-Lu, YU Chun-Lei, LIAN Sen, LI Bao-Hua, LIANG Wen-Xing, WANG Cai-Xia. Prokaryotic Expression of Xylanase VmXyl1 Gene in Valsa mali and Preparation of Polyclonal Antibody. 农业生物技术学报, 2019, 27(2): 315-322.
链接本文:  
http://journal05.magtech.org.cn/Jwk_ny/CN/10.3969/j.issn.1674-7968.2019.02.014     或     http://journal05.magtech.org.cn/Jwk_ny/CN/Y2019/V27/I2/315
 
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