Sosio M, Madoń J, Hütter R
Institute of Microbiology, Swiss Federal Institute of Technology, Zürich.
Mol Gen Genet. 1989 Jul;218(1):169-76. doi: 10.1007/BF00330580.
Streptomyces glaucescens GLA000 contains the integrated 15 kb DNA element pIJ408 which, during mating of the parent strain with S. lividans, can be transferred into recipient cells. In S. lividans cells, pIJ408 was found in an autonomously replicating form and in a chromosomally integrated state. In the majority of the S. lividans transconjugants studied, a deletion derivative pIJ408.1 (12.4 kb) occurred. The deletion form was found in some strains only as a free plasmid, in others it was also chromosomally integrated. The integration region of pIJ408 was subcloned and precisely mapped by hybridization, restriction and sequencing analyses. The DNA junction fragments of the integrated plasmid in S. glaucescens, as well as the DNA fragment containing the attachment site of the S. lividans chromosome, were also cloned, submitted to detailed restriction analysis and sequenced. The attachment site of pIJ408 (attP) and the junctions of its integrated form with the chromosomal DNA in S. glaucescens (attL and attR) contain an identical 43 bp sequence. The chromosomal attachment site in S. lividans (attB) differs from the S. glaucescens att sequence by a single base substitution. The similarities between attachment sites of SLP1, pMEA100, pSAM2 and pIJ408 are discussed.
淡青链霉菌GLA000含有整合的15 kb DNA元件pIJ408,在亲本菌株与变铅青链霉菌的接合过程中,该元件可转移至受体细胞。在变铅青链霉菌细胞中,发现pIJ408呈自主复制形式和染色体整合状态。在所研究的大多数变铅青链霉菌接合子中,出现了一种缺失衍生物pIJ408.1(12.4 kb)。这种缺失形式在一些菌株中仅作为游离质粒存在,在另一些菌株中也整合到了染色体上。通过杂交、限制性内切酶分析和测序分析,对pIJ408的整合区域进行了亚克隆并精确绘制图谱。还克隆了淡青链霉菌中整合质粒的DNA连接片段以及包含变铅青链霉菌染色体附着位点的DNA片段,对其进行了详细的限制性内切酶分析并测序。pIJ408的附着位点(attP)及其在淡青链霉菌中与染色体DNA的整合形式的连接位点(attL和attR)包含相同的43 bp序列。变铅青链霉菌中的染色体附着位点(attB)与淡青链霉菌的附着序列相差一个单碱基替换。文中讨论了SLP1、pMEA100、pSAM2和pIJ408附着位点之间的相似性。