Sezonov G V, Isaeva L M, Lomovskaia N D
Antibiot Khimioter. 1990 Dec;35(12):7-11.
The chlortetracycline (CT) resistance gene ctr was cloned from S. aureofaciens 633, a strain producing the antibiotic. The 6.6-kb DNA Bam HI fragment containing the resistance gene was cloned with the plasmid vector pIJ699. Comparison of the restriction maps of the cloned gene and the oxytetracycline (OT) resistance gene otrA from S. rimosus revealed their similarity which enabled identification of the cloned resistance gene as otrA. Investigation of the resistance determinants in S. aureofaciens 633 made it possible to identify a mtr gene(s). It was demonstrated that introduction of a ctrA gene into S. lividance provided a simultaneous increase in the resistance of the recipient strain to CT and a number of macrolide antibiotics. The CT resistance determinants in S. lividans TK64 showed properties of exogenous induction by CT and the macrolide antibiotics similar to the properties of the mtr gene(s) of S. aureofaciens. Possible adaptation properties of mtr genes are discussed.
从生产抗生素的金色链霉菌633中克隆了金霉素(CT)抗性基因ctr。将含有抗性基因的6.6kb DNA Bam HI片段与质粒载体pIJ699进行克隆。对克隆基因的限制性图谱与龟裂链霉菌的土霉素(OT)抗性基因otrA进行比较,发现它们具有相似性,从而能够将克隆的抗性基因鉴定为otrA。对金色链霉菌633中的抗性决定因素进行研究,使得鉴定出一个mtr基因成为可能。结果表明,将ctrA基因导入变铅青链霉菌可使受体菌株对CT和多种大环内酯类抗生素的抗性同时增加。变铅青链霉菌TK64中的CT抗性决定因素表现出由CT和大环内酯类抗生素进行外源诱导的特性,类似于金色链霉菌的mtr基因的特性。讨论了mtr基因可能的适应特性。