Castric P A, Sidberry H F, Sadoff J C
Department of Biological Sciences, Duquesne University, Pittsburgh, PA 15282.
Mol Gen Genet. 1989 Mar;216(1):75-80. doi: 10.1007/BF00332233.
The pilin structural gene of Pseudomonas aeruginosa 1244 was cloned in both cosmids and lambda. Expression of the cloned gene was detected in P. aeruginosa strains PAO2003, PA103, and 653A by an immunoblot reaction utilizing monoclonal antibodies. Western blot analysis showed that pilin expressed from the cloned gene was slightly larger than native 1244 pilin when produced in strains PAO2003 and 653A, but distinctly smaller in PA103. Bacteriophages specific for the 1244 pilus did not lyse strain PAO2003 containing the cloned 1244 pilin gene, indicating that functional 1244 pili were not assembled in this recombinant strain. Nucleotide sequencing revealed a coding region which when translated would produce a 15,615 dalton peptide. The amino-terminal region of this peptide is identical with published pilin sequences. While the rest of the peptides are generally dissimilar, common residues are seen within potentially antigenic regions.
铜绿假单胞菌1244的菌毛蛋白结构基因被克隆到黏粒和λ噬菌体中。利用单克隆抗体通过免疫印迹反应在铜绿假单胞菌菌株PAO2003、PA103和653A中检测到克隆基因的表达。蛋白质印迹分析表明,当在PAO2003和653A菌株中产生时,从克隆基因表达的菌毛蛋白比天然1244菌毛蛋白略大,但在PA103中明显较小。针对1244菌毛的噬菌体不能裂解含有克隆的1244菌毛蛋白基因的PAO2003菌株,这表明在该重组菌株中没有组装功能性的1244菌毛。核苷酸测序揭示了一个编码区,该编码区翻译后会产生一个15,615道尔顿的肽。该肽的氨基末端区域与已发表的菌毛蛋白序列相同。虽然其余的肽通常不同,但在潜在的抗原区域内可以看到共同的残基。