Terawaki Y, Kobayashi Y
J Bacteriol. 1978 Aug;135(2):300-6. doi: 10.1128/jb.135.2.300-306.1978.
Incompatibility of the R plasmid Rts1 and its replication mutant pTW2 was studied in recA host cells of Escherichia coli. When the R plasmid R401, belonging to the same incompatibility group as Rts1, was used as a test plasmid, R401 was eliminated preferentially from (Rts-R401)+ cells irrespective of the direction of transfer. In contrast, pTW2 and R401 were mutually excluded. The decreased incompatibility of pTW2 was confirmed by a direct incompatibility test in which a derivative of Rts1 expelled pTW2 exclusively. Alkaline sucrose gradients of pTW2 and Rts1 DNA indicated that approximately one-fourth of the Rts1 genome was deleted in pTW2. In addition, both the various temperature-dependent properties of Rts1 and the inhibitory effect on phage T4 development were also lost in pTW2. A possible mechanism that regulates the stringent replication of Rts1 is discussed.
在大肠杆菌的recA宿主细胞中研究了R质粒Rts1及其复制突变体pTW2的不相容性。当与Rts1属于同一不相容群的R质粒R401用作测试质粒时,无论转移方向如何,R401都优先从(Rts-R401)+细胞中消除。相反,pTW2和R401相互排斥。通过直接不相容性测试证实了pTW2不相容性的降低,在该测试中,Rts1的衍生物专门排出了pTW2。pTW2和Rts1 DNA的碱性蔗糖梯度表明,pTW2中Rts1基因组约四分之一被删除。此外,pTW2中还丧失了Rts1的各种温度依赖性特性以及对噬菌体T4发育的抑制作用。讨论了调节Rts1严格复制的可能机制。