Hanafusa T, Kinashi H
Mitsubishi Kasei Institute of Life Sciences, Tokyo, Japan.
Mol Gen Genet. 1992 Feb;231(3):363-8. doi: 10.1007/BF00292704.
In NF strain 2612 of Streptomyces coelicolor, a giant linear plasmid SCP1 is integrated into the chromosome at the 9 o'clock position. To characterize the integrated structure of SCP1, cloning and sequence analysis of the two junctions between the SCP1 DNA and the chromosomal DNA was carried out. The left junction was revealed to retain an almost intact left terminus of SCP1. On the other hand, the right junction was composed of IS466, deleting completely the right terminal inverted repeat of SCP1. This junction might have been formed by recombination of two IS466 elements, one present at the end of the right terminal inverted repeat of SCP1 and one on the chromosome. Based on these results, we have proposed a model for the integration of SCP1 into the chromosome. The unique conjugal transfer of NF strains and the origin of the chromosomal antibiotic biosynthetic genes in Streptomyces species are also discussed in relation to this model.
在天蓝色链霉菌的NF菌株2612中,一个巨大的线性质粒SCP1整合到染色体的9点钟位置。为了表征SCP1的整合结构,对SCP1 DNA与染色体DNA之间的两个连接点进行了克隆和序列分析。结果显示,左连接点保留了几乎完整的SCP1左末端。另一方面,右连接点由IS466组成,完全删除了SCP1的右末端反向重复序列。这个连接点可能是由两个IS466元件重组形成的,一个位于SCP1右末端反向重复序列的末端,另一个位于染色体上。基于这些结果,我们提出了一个SCP1整合到染色体中的模型。还结合这个模型讨论了NF菌株独特的接合转移以及链霉菌属中染色体抗生素生物合成基因的起源。