Khater Letícia, Alegria Marcos C, Borin Paula F L, Santos Túlio M, Docena Cássia, Tasic Ljubica, Farah Chuck S, Ramos Carlos H I
Laboratório Nacional de Luz Síncrotron, CEP 13084-971 Campinas, SP, Brazil.
Arch Microbiol. 2007 Sep;188(3):243-50. doi: 10.1007/s00203-007-0240-y. Epub 2007 May 10.
Genome annotation of the plant pathogen Xanthomonas axonopodis pv. citri (Xac), identified flagellar genes in a 15.7 kb gene cluster. However, FlgN, a secretion chaperone for hook-associated proteins FlgK and FlgL, was not identified. We performed extensive screening of the X. axonopodis pv. citri genome with the yeast two-hybrid system to identify a protein with the characteristics of the flagellar chaperone FlgN. We found a candidate (XAC1990) encoded by an operon for components of the flagellum apparatus that interacted with FlgK. In order to further support this finding, Xac FlgK and XAC1990 were cloned, expressed, and purified. The recombinant proteins were characterized by spectroscopic methods and their interaction in vitro confirmed by pull-down assays. We, therefore, conclude that XAC1990 and its homologs in other Xanthomonas species are, in fact, FlgN proteins. These observations extend the sequence diversity covered by this family of proteins.
植物病原菌柑桔溃疡病菌(Xanthomonas axonopodis pv. citri,Xac)的基因组注释在一个15.7 kb的基因簇中鉴定出了鞭毛基因。然而,未鉴定出与钩相关蛋白FlgK和FlgL的分泌分子伴侣FlgN。我们利用酵母双杂交系统对柑桔溃疡病菌基因组进行了广泛筛选,以鉴定具有鞭毛分子伴侣FlgN特征的蛋白。我们发现了一个由鞭毛装置组件操纵子编码的候选蛋白(XAC1990),它与FlgK相互作用。为了进一步支持这一发现,克隆、表达并纯化了Xac FlgK和XAC1990。通过光谱方法对重组蛋白进行了表征,并通过下拉试验证实了它们在体外的相互作用。因此,我们得出结论,XAC1990及其在其他黄单胞菌属物种中的同源物实际上是FlgN蛋白。这些观察结果扩展了该蛋白家族所涵盖的序列多样性。