Wang C Y, Bond V C, Genco C A
Department of Biochemistry, Morehouse School of Medicine, Atlanta, Georgia 30310, USA.
J Bacteriol. 1997 Jun;179(11):3808-12. doi: 10.1128/jb.179.11.3808-3812.1997.
In this study a second endogenous Porphyromonas gingivalis insertion element (IS element) that is capable of transposition within P. gingivalis was identified. Nucleotide sequence analysis of the Tn4351 insertion site in a P. gingivalis Tn4351-generated transconjugant showed that a complete copy of the previously unidentified IS element, designated PGIS2, had inserted into IS4351R in Tn4351. PGIS2 is 1,207 bp in length with 19-bp imperfect terminal inverted repeats, and insertion resulted in a duplicated 10-bp target sequence. Results of Southern hybridization of chromosomal DNA isolated from several P. gingivalis strains with a PGIS2-specific probe demonstrated that the number of copies of PGIS2 per genome varies among different P. gingivalis strains. Computer analysis of the putative polypeptide encoded by PGIS2 revealed strong homologies to the products encoded by IS1358 from Vibrio cholerae, ISAS1 from Aeromonas salmonicida, and H-rpt in Escherichia coli K-12.
在本研究中,鉴定出了第二种能够在牙龈卟啉单胞菌内转座的内源性牙龈卟啉单胞菌插入元件(IS元件)。对一株牙龈卟啉单胞菌Tn4351产生的接合子中Tn4351插入位点的核苷酸序列分析表明,一个先前未鉴定的IS元件(命名为PGIS2)的完整拷贝已插入Tn4351中的IS4351R。PGIS2长度为1207 bp,具有19 bp的不完全末端反向重复序列,插入导致一个重复的10 bp靶序列。用PGIS2特异性探针与从几种牙龈卟啉单胞菌菌株中分离的染色体DNA进行Southern杂交的结果表明,不同牙龈卟啉单胞菌菌株中每个基因组的PGIS2拷贝数各不相同。对PGIS2编码的假定多肽进行计算机分析发现,它与霍乱弧菌的IS1358、杀鲑气单胞菌的ISAS1以及大肠杆菌K-12中的H-rpt编码的产物具有很强的同源性。