Fetherston J D, Perry R D
Department of Microbiology and Immunology, University of Kentucky, Lexington 40536-0084.
Mol Microbiol. 1994 Aug;13(4):697-708. doi: 10.1111/j.1365-2958.1994.tb00463.x.
The pigmentation (Pgm+) phenotype of Yersinia pestis includes a number of different characteristics which appear to be associated with a 102 kb segment of chromosomal DNA known as the pgm locus. In Y. pestis KIM6+, the pgm locus is flanked by direct copies of a repeated element that probably plays a role in the spontaneous deletion of this region. We have sequenced the ends of these elements and shown that they have features in common with bacterial insertion sequences. In addition we show that a clone, pSDR498, from the pgm locus of KIM6+ restores pesticin sensitivity and the iron-regulated expression of three polypeptides, 240 kDa, 190 kDa, and 68 kDa in size, to Pgm- cells. In vitro transcription/translation assays and Escherichia coli minicells were used to analyse the products encoded by various subclones of pSDR498. Pesticin sensitivity mapped to a 5.9 kb fragment that encodes a 68 kDa protein derived from a 72 kDa precursor. Synthesis of the 190 kDa protein was restored by a 19.2 kb clone, indicating that the structural gene for this protein also resides within the pgm locus of Y. pestis KIM6+. Finally, a survey of our Pgm- strains indicates that 97% have also deleted the sequences encoding the 190 kDa protein and pesticin sensitivity.
鼠疫耶尔森菌的色素沉着(Pgm+)表型包括许多不同特征,这些特征似乎与一段102 kb的染色体DNA片段有关,该片段被称为pgm基因座。在鼠疫耶尔森菌KIM6+中,pgm基因座两侧是一个重复元件的直接拷贝,该重复元件可能在该区域的自发缺失中起作用。我们对这些元件的末端进行了测序,结果表明它们具有与细菌插入序列相同的特征。此外,我们还表明,来自KIM6+的pgm基因座的一个克隆pSDR498可恢复Pgm-细胞对杀鼠疫菌素的敏感性以及三种大小分别为240 kDa、190 kDa和68 kDa的多肽的铁调节表达。体外转录/翻译分析和大肠杆菌微小细胞被用于分析pSDR498的各种亚克隆所编码的产物。杀鼠疫菌素敏感性定位于一个5.9 kb的片段,该片段编码一种由72 kDa前体衍生而来的68 kDa蛋白质。一个19.2 kb的克隆恢复了190 kDa蛋白质的合成,这表明该蛋白质的结构基因也位于鼠疫耶尔森菌KIM6+的pgm基因座内。最后,对我们的Pgm-菌株的一项调查表明,97%的菌株也缺失了编码190 kDa蛋白质和杀鼠疫菌素敏感性的序列。