Stalker D M, Helinski D R
Plasmid. 1985 Nov;14(3):245-54. doi: 10.1016/0147-619x(85)90008-3.
The expression of incompatibility properties between the IncX plasmids R6K and R485 of Escherichia coli was examined. For small autonomously replicating derivatives of both plasmid elements, the requirements for incompatibility expression include a functional R485 replicon and an active R6K beta-origin region. Functional R6K alpha and gamma origins are not directly involved in incompatibility expression between R6K and R485. A trans-acting replication system was constructed for plasmid R485. It consists of a 3.2-(kb) DNA fragment of R485 that specifies a product(s) in trans which supports replication from an R485 origin plasmid. A minimal R485 origin region of 591 bp was derived utilizing this trans-acting replication system and the nucleotide sequence of this origin region determined. The most striking feature of the sequence is the presence of six tandem 22-bp nucleotide sequence direct repeats.
对大肠杆菌IncX质粒R6K和R485之间不相容性特性的表达进行了研究。对于这两种质粒元件的小型自主复制衍生物,不相容性表达的要求包括一个功能性的R485复制子和一个活性的R6Kβ-起源区域。功能性的R6Kα和γ起源并不直接参与R6K和R485之间的不相容性表达。构建了一个用于质粒R485的反式作用复制系统。它由R485的一个3.2(kb)DNA片段组成,该片段在反式中指定一种产物,支持从R485起源质粒进行复制。利用这个反式作用复制系统获得了一个591 bp的最小R485起源区域,并确定了该起源区域的核苷酸序列。该序列最显著的特征是存在六个串联的22 bp核苷酸序列直接重复。