Sodeinde O A, Goguen J D
Department of Molecular Genetics and Microbiology, University of Massachusetts Medical School, Worcester 01655.
Infect Immun. 1989 May;57(5):1517-23. doi: 10.1128/iai.57.5.1517-1523.1989.
We have determined the nucleotide sequence of the 1.4-kilobase DNA fragment containing the plasminogen activator gene (pla) of Yersinia pestis, which determines both plasminogen activator and coagulase activities of the species. The sequence revealed the presence of a 936-base-pair open reading frame that constitutes the pla gene. This reading frame encodes a 312-amino-acid protein of 34.6 kilodaltons and containing a putative 20-amino-acid signal sequence. The presence of a single large open reading frame is consistent with our previous conclusion that the two Pla proteins which appear in the outer membrane of pla+ Y. pestis are derived from a common precursor. The deduced amino acid sequence of Pla revealed that it possesses a high degree of homology to the products of gene E of Salmonella typhimurium and ompT of Escherichia coli but does not possess significant homology to other plasminogen activators of known sequence. We also identified a transcription unit that resides on the complimentary strand and overlaps the pla gene.
我们已经确定了包含鼠疫耶尔森菌纤溶酶原激活剂基因(pla)的1.4千碱基DNA片段的核苷酸序列,该基因决定了该物种的纤溶酶原激活剂和凝固酶活性。该序列显示存在一个构成pla基因的936个碱基对的开放阅读框。这个阅读框编码一个34.6千道尔顿的312个氨基酸的蛋白质,并含有一个推定的20个氨基酸的信号序列。单个大的开放阅读框的存在与我们之前的结论一致,即出现在pla +鼠疫耶尔森菌外膜中的两种Pla蛋白来自一个共同的前体。Pla的推导氨基酸序列显示,它与鼠伤寒沙门氏菌的基因E产物和大肠杆菌的ompT具有高度同源性,但与已知序列的其他纤溶酶原激活剂没有显著同源性。我们还鉴定了一个位于互补链上并与pla基因重叠的转录单元。