Mozola M A, Wilson R B, Jordan E M, Draper R K, Clowes R C
J Bacteriol. 1984 Aug;159(2):683-7. doi: 10.1128/jb.159.2.683-687.1984.
Using the broad-host-range plasmid vector pRO1614, we cloned a segment of the gene from Pseudomonas aeruginosa PA103 encoding the enzymatically active part of the exotoxin A protein. Expression of the cloned gene segment has been achieved both in Escherichia coli and in a nontoxigenic P. aeruginosa host, as assayed by the production of exotoxin A-related antigen and by the ability of the gene product to ADP-ribosylate elongation factor 2. Western blot hybridization analysis revealed a series of polypeptides antigenically related to exotoxin A, the largest of which had a molecular weight of ca. 50,000.
利用广宿主范围质粒载体pRO1614,我们从铜绿假单胞菌PA103中克隆了一段基因,该基因编码外毒素A蛋白的酶活性部分。通过外毒素A相关抗原的产生以及基因产物对延伸因子2进行ADP核糖基化的能力检测发现,克隆的基因片段在大肠杆菌和无毒铜绿假单胞菌宿主中均已实现表达。蛋白质印迹杂交分析揭示了一系列与外毒素A抗原相关的多肽,其中最大的一种分子量约为50,000。