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花椒窄吉丁气味结合蛋白AzanOBP5的克隆与表达
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引用本文:郭莉,陈迪,贾任航,高晓进,张泽腾,谢寿安,吕淑杰.花椒窄吉丁气味结合蛋白AzanOBP5的克隆与表达.植物保护学报,2023,50(1):81-90
DOI:10.13802/j.cnki.zwbhxb.2023.2021078
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作者单位E-mail
郭莉 西北农林科技大学林学院, 陕西 杨凌 712100  
陈迪 西北农林科技大学林学院, 陕西 杨凌 712100  
贾任航 西北农林科技大学林学院, 陕西 杨凌 712100  
高晓进 西北农林科技大学林学院, 陕西 杨凌 712100  
张泽腾 西北农林科技大学林学院, 陕西 杨凌 712100  
谢寿安 西北农林科技大学林学院, 陕西 杨凌 712100 shouanxie@163.com 
吕淑杰 西北农林科技大学林学院, 陕西 杨凌 712100  
中文摘要:为进一步明确花椒窄吉丁Agrilus zanthoxylumi气味结合蛋白AzanOBP5在昆虫嗅觉识别过程中的功能,基于花椒窄吉丁转录组数据(SUB6796283)利用cDNA末端快速扩增技术对花椒窄吉丁气味结合蛋白基因AzanOBP5进行全长克隆并进行生物信息学分析;通过实时荧光定量检测技术测定基因AzanOBP5在成虫不同组织中的表达情况。结果显示,克隆获得基因AzanOBP5全长740bp(GenBank登录号为MT318834),5'端非编码区为172bp,3'端非编码区114bp,开放阅读框453bp,编码150个氨基酸。序列分析表明,AzanOBP5氨基酸序列与苹果小吉丁Agrilus mali AmalOBP5的氨基酸序列一致性最高。成功构建pET-21a-AzanOBP5重组质粒并在大肠杆菌Escherichia coli中表达,经过诱导和纯化条件的优化及Western blot鉴定,得到的融合蛋白His-AzanOBP5大小符合预期。基因AzanOBP5在雌雄成虫的不同组织中均有表达,其中在成虫腹部的表达量最高。表明花椒窄吉丁气味结合蛋白基因AzanOBP5除参与嗅觉识别过程外,还可能具有其他生理功能。
中文关键词:花椒窄吉丁  气味结合蛋白  基因克隆  组织表达  原核表达
 
Cloning and expression of the odorant binding protein AzanOBP5 in pepper buprestid beetle Agrilus zanthoxylumi
Author NameAffiliationE-mail
GUO Li College of Forestry, Northwest A&F University, Yangling 712100, Shaanxi Province, China  
CHEN Di College of Forestry, Northwest A&F University, Yangling 712100, Shaanxi Province, China  
JIA Ren-hang College of Forestry, Northwest A&F University, Yangling 712100, Shaanxi Province, China  
GAO Xiao-jin College of Forestry, Northwest A&F University, Yangling 712100, Shaanxi Province, China  
ZHANG Ze-teng College of Forestry, Northwest A&F University, Yangling 712100, Shaanxi Province, China  
XIE Shou-an College of Forestry, Northwest A&F University, Yangling 712100, Shaanxi Province, China shouanxie@163.com 
Lü Shu-jie College of Forestry, Northwest A&F University, Yangling 712100, Shaanxi Province, China  
Abstract:To clarify the function of AzanOBP5, an odorant binding protein in pepper buprestid beetle Agrilus zanthoxylumi, in insect olfactory recognition. RACE technology was used to clone the fulllength cDNA of AzanOBP5 based on the transcriptome data of A. zanthoxylumi(SUB6796283). The nucleotide and deduced amino acid sequences were analyzed by bioinformatics software. The expression levels of AzanOBP5 in different tissues of adult were determined by real time quantitative PCR. The full-length cDNA of AzanOBP5 was 740 bp(GenBank accession no.: MT318834), with a non-coding region of 172 bp and 114 bp at the 5' and 3' ends, respectively. The open reading frame was 453 bp, encoding 150 amino acids. Homologous sequence alignment analyses showed that AzanOBP5 had the highest amino acid sequence identity with AmalOBP5 from A. mali. The recombinant plasmid pET-21a-AzanOBP5 was successfully constructed and expressed in E. coli. After optimization of the induction and purification conditions, it was identified by Western blot. The obtained fusion protein His-AzanOBP5 was in line with expectations. The gene AzanOBP5 was expressed in various tissues of both male and female adults, and the highest expression level was detected in abdomen. The study showed that AzanOBP5 not only played a role in olfactory recognition, but also had other physiological functions in A. zanthoxylumi.
keywords:Agrilus zanthoxylumi  odorant binding protein  gene clone  tissue expression  prokaryotic expression
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