绿脓杆菌ATCC9027外毒素PE40基因克隆与系统发育分析  

Cloning and phylogenetic analysis of PE40 gene of pseudomonas aeruginosa ATCC9027 exotoxin

作　　者：刘红彬[1] 顾小龙[1] 

机构地区：[1]河北北方学院,河北张家口075000

出　　处：《中国老年学杂志》2013年第19期4769-4771,共3页Chinese Journal of Gerontology

基　　金：河北省中医药管理局课题(No.2011100);河北省教育厅课题(No.Z2010117);张家口市科技局课题(1112013C-3)

摘　　要：目的为获得用于构建免疫毒素弹头的毒素蛋白基因,克隆绿脓杆菌外毒素PE40基因。方法 PCR扩增ATCC9027外毒素PE40基因,纯化PCR产物与T载体连接后转染感受态大肠杆菌JM109,蓝白斑筛选阳性克隆,HindⅢ酶切和测序鉴定阳性克隆。将ATCC9027的PE40基因进行blast搜索,以Genbank中所有的绿脓杆菌外毒素PE40基因为内群,以白喉毒素基因为外群进行系统发育分析。结果 PCR产物为1 098 bp。与PA103相比,ATCC9027外毒素PE40基因有14个碱基的突变,导致外毒素蛋白8个氨基酸的突变。系统发育树显示绿脓杆菌外毒素PE40基因形成单系群,ATCC9027和ATCC927853的亲缘关系最近。结论 ATCC9027外毒素关键位点的氨基酸未发生突变,获得了用于构建免疫毒素弹头的毒素蛋白基因PE40。Objective To obtain the toxin gene PE40,which acts as the warhead of ＂biological missites＂.Methods Primers was designed according to the exotoxin gene of pseudomonas aeruginosa strain 103,and a HindⅢ site was introduced for development of expressing vector.PE40 gene was amplified from genome DNA of pseudomonas aeruginosa ATCC9027 by PCR,then the purified PCR product was cloned into the pMD18-T simple vector.The recombinant was identified by simple digestion （HindⅢ） and sequencing.Results The PCR product was 1 098 bp.Compared with Pseudomonas aeruginosa 103,PE40 gene of ATCC9027 produced 14 bp mutations.The mutations of 14 bp resulted in the mutations of eight amino acids,but the eight amino acids were not critical situs,and the mutations didn＇t affect enzymatic activity and cytotoxicity of the exotoxin.The phylogenetic tree indicated that PE40 gene matrix of pseudomonas aeruginosa exotoxin formed a monophyletic group.Pseudomonas aeruginosa ATCC9027 and ATCC27853 formed a branch,and had closest relationship.Conclusions PE40 gene to construct immunotoxin was obstained.

关 键 词：绿脓杆菌外毒素（PE） 除去细胞识别部分Ia的绿脓杆菌外毒素（PE40） 克隆 

分 类 号：Q933[生物学—微生物学]