Ounissi H, Courvalin P
Gene. 1985;35(3):271-8. doi: 10.1016/0378-1119(85)90005-8.
We have cloned and determined the nucleotide sequence of the gene ereA of plasmid pIP1100 which confers high-level resistance to erythromycin (Em) in Escherichia coli. The gene was defined by initiation and termination codons and by in vitro insertion-inactivation into an open reading frame (ORF) of 1032 bp corresponding to a product with an Mr of 37 765. However, the enzyme, an Em esterase, displayed an apparent Mr of 43 000 upon electrophoresis of a minicell extract on the SDS-polyacrylamide gels. The G + C content (50.5%) of the gene ereA and the preferential codon usage in its ORF suggest that this resistance determinant should be indigenous to E. coli.
我们已经克隆并测定了质粒pIP1100的ereA基因的核苷酸序列,该基因赋予大肠杆菌对红霉素(Em)的高水平抗性。该基因由起始密码子和终止密码子以及通过体外插入失活确定为一个1032 bp的开放阅读框(ORF),其对应的产物分子量为37765。然而,该酶(一种Em酯酶)在SDS-聚丙烯酰胺凝胶上对小细胞提取物进行电泳时,表观分子量为43000。ereA基因的G + C含量(50.5%)及其ORF中的优先密码子使用情况表明,这种抗性决定簇应该是大肠杆菌所固有的。