Roggenkamp A, Schubert S, Jacobi C A, Heesemann J
Institut für Hygiene und Mikrobiologie, Universität Würzburg, Germany.
FEMS Microbiol Lett. 1995 Dec 1;134(1):69-73. doi: 10.1111/j.1574-6968.1995.tb07916.x.
The structural genes encoding the Yop proteins of Yersinia enterocolitica are scattered around on the virulence plasmid (pYV). The genes which are required for transactivation, secretion and translocation of the Yopos are encoded in one cluster known as the lcr-region of pYV. After the introduction of an additional SalI restriction site into pYV of Y. enterocolitica serotype O8, we were able to clone and isolate the whole lcr-region on the mobilizable low copy vector pSUP102. Analysis of this construct in a plasmidless WA-strain showed that all Yops being encoded inside the lcr-region (YopN, YopB, YopD and the V-antigen) were secreted into the culture supernatant. Moreover, this lcr-fragment was able to promote secretion of other Yops encoded by a second recombinant plasmid. Thus the translocation and function of single Yops can be studied.
编码小肠结肠炎耶尔森菌Yop蛋白的结构基因分散在毒力质粒(pYV)上。Yop蛋白的反式激活、分泌和转运所需的基因编码在一个称为pYV的lcr区域的簇中。在小肠结肠炎耶尔森菌O8血清型的pYV中引入一个额外的SalI限制性酶切位点后,我们能够在可移动的低拷贝载体pSUP102上克隆并分离出整个lcr区域。在无质粒的WA菌株中对该构建体进行分析表明,lcr区域内编码的所有Yop蛋白(YopN、YopB、YopD和V抗原)都分泌到了培养上清液中。此外,这个lcr片段能够促进由第二个重组质粒编码的其他Yop蛋白的分泌。因此,可以研究单个Yop蛋白的转运和功能。