Charpentier E, Gerbaud G, Courvalin P
Unité des Agents Antibactériens, Institut Pasteur, Paris, France.
Gene. 1993 Sep 6;131(1):27-34. doi: 10.1016/0378-1119(93)90665-p.
The nucleotide sequence of the tetracycline (Tc)-minocycline (Mc)-resistance determinant of plasmid pIP811 from Listeria monocytogenes BM4210 has been determined. The gene, designated tet(S), was identified by analysis of the start and stop codons as a coding sequence of 1923 bp, corresponding to a protein with a calculated M(r) of 72,912. The apparent 68-kDa size estimated by sodium dodecyl sulfate-polyacrylamide-gel electrophoresis of the protein characterized in a cell-free coupled transcription-translation system was in good agreement with the calculated value. The tet(S) gene product exhibits 79 and 72% amino acid identity with Tet(M) from Streptococcus pneumoniae and Tet(O) from Campylobacter coli, respectively. The distribution of tet(S) in strains of Gram+ and Gram- genera resistant to Tc (TcR) and Mc (McR) was studied by hybridization under high stringency using a 590-bp intragenic probe. Homology with tet(S) was detected in two clinical isolates of L. monocytogenes isolated in different geographical areas.
已测定了来自单核细胞增生李斯特菌BM4210的质粒pIP811的四环素(Tc)-米诺环素(Mc)抗性决定簇的核苷酸序列。通过对起始密码子和终止密码子的分析鉴定出该基因,命名为tet(S),其编码序列为1923 bp,对应一种计算分子量(M(r))为72,912的蛋白质。在无细胞偶联转录-翻译系统中对该蛋白质进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳估计的表观大小为68 kDa,与计算值高度一致。tet(S)基因产物与肺炎链球菌的Tet(M)和大肠弯曲菌的Tet(O)的氨基酸同一性分别为79%和72%。使用590 bp的基因内探针在高严谨度下通过杂交研究了tet(S)在对Tc(TcR)和Mc(McR)耐药的革兰氏阳性和革兰氏阴性菌属菌株中的分布。在不同地理区域分离的两株单核细胞增生李斯特菌临床分离株中检测到与tet(S)的同源性。