Miki T, Easton A M, Rownd R H
Mol Gen Genet. 1978 Jan 17;158(3):217-24. doi: 10.1007/BF00267192.
The drug resistance genes on the r-determinants component of the composite R plasmid NR1 were mapped on the EcoRI restriction endonuclease fragments of the R plasmid by cloning the fragments using the plasmid RSF2124 as a vector. The sulfonamide (Su) and streptomycin/spectinomycin (Sm/Sp) resistance genes are located on EcoRI fragment G of NR1. The expression of resistance to mercuric ions (Mer) requires both EcoRI fragment H and I of NR1. The expression of chloramphenicol (Cm) and fusidic acid (Fus) resistance requires EcoRI fragments A and J of NR1. The kan fragment of the related R plasmid R6-5 can substitute for Eco RI fragment J of NR1 in the expression of Cm and Fus resistance. The structural genes for Cm and Fus resistance appear to be a part of an operon whose expression is controlled by the same promoter.
通过使用质粒RSF2124作为载体克隆复合R质粒NR1的片段,将复合R质粒NR1的r-决定簇成分上的耐药基因定位在R质粒的EcoRI限制性内切酶片段上。磺胺(Su)和链霉素/壮观霉素(Sm/Sp)耐药基因位于NR1的EcoRI片段G上。对汞离子(Mer)耐药性的表达需要NR1的EcoRI片段H和I。氯霉素(Cm)和夫西地酸(Fus)耐药性的表达需要NR1的EcoRI片段A和J。相关R质粒R6-5的kan片段在Cm和Fus耐药性的表达中可替代NR1的EcoRI片段J。Cm和Fus耐药性的结构基因似乎是一个操纵子的一部分,其表达由同一个启动子控制。