@ARTICLE{Bahrmand, author = {Faezi, Sobhan and Bahrmand, Ahmad Reza and Mahdavi, Mehdi and Siadat, Seyed Davar and Nikokar, Iraj and Sardari, Soroush and Holder, Ian Alan and }, title = {High Yield Overexpression, Refolding, Purification and Characterization of Pseudomonas aeruginosa Type B-Flagellin: An Improved Method Without Sonication}, volume = {5}, number = {1}, abstract ={Pseudomonas aeruginosa as an opportunistic pathogen is a significant cause of acute and chronic infections in patients with compromised defenses. This bacterium is motile via a single polar flagellum made of polymerized flagellin subunits differentiated into two major serotypes: A and B. flagellin plays an important role as a virulence factor in the adhesion, colonization and invasion of P. aeruginosa into host epithelial cells. To develop a functional vaccine that can be used in practical application to prevent and treat infection, type B-flagellin was produced as recombinant protein. In this work, the fliC gene was introduced into a pET28a vector and expressed in Escherichia coli BL21 (DE3). The expressed recombinant protein was purified by a modified method without sonication using a HisTrap affinity column. The functional activities of produced flagellin were confirmed by ELISA, western blot analysis, motility inhibition assay and opsonophagocytosis test. The purification process of the type B-flagellin was lead to a high yield. The produced recombinant type B-flagellin showed high biological activity in all of these standard assays. In conclusions, this report provides the new protocol to efficiently obtain the type B-flagellin with high biological activity and immunogenicity. This immunogen can be introduced as an adjuvant or vaccine in the future study. }, URL = {http://ijmcmed.org/article-1-437-en.html}, eprint = {http://ijmcmed.org/article-1-437-en.pdf}, journal = {International Journal of Molecular and Cellular Medicine}, doi = {10.22088/acadpub.BUMS.5.1.37}, year = {2016} }