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孔石莼凝集素蛋白基因的克隆与表达

Cloning and Expression of Lectin Gene of Ulva pertusa

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【作者】 郑璐平谢荔岩姚锦爱钟伏弟林奇英吴祖建谢联辉

【Author】 ZHENG Lu-pinga,b,XIE Li-yana,YAO Jin-aia,ZHONG Fu-dia,LIN Qi-yinga,WU Zu-jiana,b,XIE Lian-huia,b(Fujian Agriculture and Forestry University a.Institute of Plant Virology;b.Key Laboratory of Biopesticide and Chemical Biology,Ministry of Education,Fuzhou 350002,Fujian,China)

【机构】 福建农林大学病毒研究所福建农林大学生物农药与化学生物学教育部重点实验室

【摘要】 根据孔石莼(Ulva pertusa)凝集素(Lectin)蛋白cDNA全长序列(GenBank登录号:AY433960)设计引物,以其总DNA为模板,采用PCR技术扩增蛋白DNA序列,经克隆、测序获得基因序列。结果表明,孔石莼凝集素蛋白(UPL)基因序列长约为670 bp,含有一个大小为56 bp的内含子。此外,设计带酶切位点的引物,以UPL-cDNA为模板,扩增其开放阅读框,并与表达载体pGEX-2T连接,构建原核表达载体pG2T-UPL,并在大肠杆菌BL21(DE3)中成功表达大小约为47 kD的目的蛋白。

【Abstract】 Based on the known cDNA sequence of lectin protein gene of U.pertusa(GenBank accession number: AY433960),a pair of primers were designed and used to clone,and sequence the lectin protein gene with PCR technique by using the genomic DNA of U.pertusa as the template.The results showed that the lectin protein gene consisted of 670 bp,with a 56 bp intron.A pair of primers with restriction enzyme sites were designed to amplify the ORF using the genomic cDNA of U.pertusa as the template.The ORF was inserted into the expression vector pGEX-2T and a protein with molecular weight of 47 kD was successfully expressed in Escherichia coli BL21(DE3).

【关键词】 孔石莼凝集素cDNA基因克隆原核表达
【Key words】 Ulva pertusaLectincDNAgene cloningprokaryotic expression
【基金】 福建省科技厅重大项目(2000H004,2001Z127)
  • 【文献出处】 激光生物学报 ,Acta Laser Biology Sinica , 编辑部邮箱 ,2008年06期
  • 【分类号】Q943.2
  • 【被引频次】2
  • 【下载频次】91
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