Tanaka M, Harafuji H, Yamamoto T
J Bacteriol. 1982 Aug;151(2):723-8. doi: 10.1128/jb.151.2.723-728.1982.
Tn2603 is a multiple-resistance transposon encoding resistance to ampicillin, streptomycin, sulfonamide, and mercury and having a molecular size of 20 kilobase pairs, with 200-base-pair inverted repeats at both ends. The essential sites and functions of Tn2603 which are required for its transposition were determined through construction and characterization of various deletion mutants affecting the efficiency of transposition. Deletions were introduced in plasmid pMK1::Tn2603 by partial digestion with restriction endonuclease EcoRI in vitro. Analysis of deletion mutants showed that the inverted repeat segments at both ends of the trans-acting diffusible product(s) encoded in the right-hand side of the central portion were required for the transposition of Tn2603. An essential gene product was revealed as a protein having a molecular weight of 110,000 by analysis of polypeptides synthesized in Escherichia coli minicells. This protein was assumed to be the so-called transposase.
Tn2603是一种多重耐药转座子,编码对氨苄青霉素、链霉素、磺胺类药物和汞的抗性,分子大小为20千碱基对,两端有200碱基对的反向重复序列。通过构建和表征影响转座效率的各种缺失突变体,确定了Tn2603转座所需的必需位点和功能。通过体外限制性内切酶EcoRI部分消化,在质粒pMK1::Tn2603中引入缺失。缺失突变体分析表明,Tn2603转座需要中央部分右侧编码的反式作用扩散产物两端的反向重复序列。通过分析在大肠杆菌微小细胞中合成的多肽,揭示了一种必需的基因产物是一种分子量为110,000的蛋白质。这种蛋白质被认为是所谓的转座酶。