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作 者:何菱[1] 胡福泉[2] 逯好英[2] 沈定霞[2] 俞树荣[2] 马贤凯[2]
机构地区:[1]第三军医大学微生物学教研室,重庆630038 [2]军事医学科学院基础所分子遗传室
出 处:《中华微生物学和免疫学杂志》1996年第2期139-142,共4页Chinese Journal of Microbiology and Immunology
摘 要:绿脓杆菌外表素A是由613个氨基酸残基组成的单链杀细胞毒素;利用PCR技术直接从绿脓杆菌染色体DNA中扩增了外毒素A的Ⅰ+Ⅱ区的结构基因,通过酶切鉴定、DNA序列分析,证实了克隆的基因片段为外毒素A的结构基因;重组表达质粒经诱导表达后SDS-pAGE及Western blot证实了表达的产物为外毒素A分子。对外毒素A的Ⅰ+Ⅱ区结构基因的克隆表达为疫苗研制、毒素类似物的制备以及导向药物的构建打下了基础。Pseudomonas exotoxin A (ETA ) is a 6 13-residue cytocidal protein. In this report , a 1 . 25kb fragment of exotoxin A Domain Ⅰ+Ⅱ structural gene of Pseudomonas aeruginosa was amplified form chromosomal DNA of Pseudomonas aeruginosa by using PCR technology. The amplified fragment was cloned into expression vector pET-3a directly. The recombinant plasmids were screened and were determined with restriction enzymes digestion. The cloned fragment was also sequenced with dideoxynucleotide termination method and automated DNA sequencing by using PCR primer to guide the sequencing. The result of the sequencing identified that the cloned gene was a fragment of ETA. SDS-PAGE assay and western blot confirmed that the expression products are ETA-related polypeptides.
分 类 号:R378.991[医药卫生—病原生物学]
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