Rubens C E, McNeill W F, Farrar W E
J Bacteriol. 1979 Sep;139(3):877-82. doi: 10.1128/jb.139.3.877-882.1979.
A 9.1 x 10(6)-dalton transposable deoxyribonucleic acid sequence resides within Pseudomonas aeruginosa plasmid R1033 and mediates resistance to gentamicin, streptomycin, sulfamethoxazole, chloramphenicol, and mercuric chloride. Transposability was demonstrated in Escherichia coli when this sequence, designated Tn1696, excised from R1033 and integrated into plasmid pMB8. Excision and insertion of Tn1696 occurred independently of the host Rec phenotype and may involve the 140-base pair, inverted deoxyribonucleic acid repeated region that flanks this sequence. Occurrence of a multiresistance transposon on a transferrable plasmid that has a broad host range may have serious epidemiological and therapeutic consequences.
一个9.1×10⁶道尔顿的可转座脱氧核糖核酸序列存在于铜绿假单胞菌质粒R1033中,并介导对庆大霉素、链霉素、磺胺甲恶唑、氯霉素和氯化汞的抗性。当这个被命名为Tn1696的序列从R1033上切除并整合到质粒pMB8中时,在大肠杆菌中证明了其可转座性。Tn1696的切除和插入独立于宿主的Rec表型,可能涉及位于该序列两侧的140个碱基对的反向脱氧核糖核酸重复区域。在具有广泛宿主范围的可转移质粒上出现多抗性转座子可能会产生严重的流行病学和治疗后果。