Jagura-Burdzy G, Thomas C M
School of Biological Sciences, University of Birmingham, Edgbaston, UK.
J Mol Biol. 1995 Oct 13;253(1):39-50. doi: 10.1006/jmbi.1995.0534.
The KorA protein of promiscuous plasmid RK2 is encoded in the central control operon, which coordinates expression of genes for replication, transfer and partitioning. KorA is known to repress transcription from seven promoters on the plasmid genome but at the trfA promoter, for the vegetative replication genes, it also causes derepression of trbAp, the first promoter for the operon whose genes are required primarily for mating pair formation prior to conjugative transfer. We have overproduced and purified KorA (101 amino acid residues). Crosslinking indicates that it exists largely as a dimer in solution. Western blotting with specific antibodies suggests that there are approximately 4000 monomers per cell in exponential phase and about 600 in stationary phase. Footprinting confirmed the expected location of the KorA operator, and indicated that KorA and RNA polymerase can bind simultaneously in promoter regions. Gel retardation experiments with DNA fragments carrying each of the seven KorA operators revealed that there is a hierarchy of binding affinities. Highest affinity (Kapp = 12 to 20 nM) occurs with operators containing the 12 bp inverted repeat GTTTAGCTAAAC (klaAp, korAp and trfAp), while lower affinities (Kapp = 136 to 272 nM) occur with less perfect repeats (klcA, kleA, kleC, kfrA). In addition, specific DNA sequences flanking the 12 bp are necessary for the characteristic type I KorA binding affinity. This hierarchy may be important in providing a graded response in expression of the operons controlled by KorA as its concentration varies, as for example on transition from exponential to stationary phase.
多功能质粒RK2的KorA蛋白由中央控制操纵子编码,该操纵子协调复制、转移和分配相关基因的表达。已知KorA可抑制质粒基因组上7个启动子的转录,但对于营养复制基因的trfA启动子,它还会导致trbAp的去抑制,trbAp是该操纵子的第一个启动子,其基因主要在接合转移前的配对形成过程中发挥作用。我们过量表达并纯化了KorA(101个氨基酸残基)。交联实验表明它在溶液中主要以二聚体形式存在。用特异性抗体进行的蛋白质免疫印迹分析表明,在指数生长期每个细胞中约有4000个单体,而在稳定期约有600个。足迹实验证实了KorA操纵子的预期位置,并表明KorA和RNA聚合酶可在启动子区域同时结合。对携带7个KorA操纵子的DNA片段进行的凝胶阻滞实验表明,存在结合亲和力的等级差异。最高亲和力(Kapp = 12至20 nM)出现在含有12 bp反向重复序列GTTTAGCTAAAC的操纵子(klaAp、korAp和trfAp)中,而较低亲和力(Kapp = 136至272 nM)则出现在不太完美的重复序列(klcA、kleA、kleC、kfrA)中。此外,12 bp侧翼的特定DNA序列对于典型的I型KorA结合亲和力是必需的。随着KorA浓度的变化,例如从指数生长期过渡到稳定期,这种等级差异对于由KorA控制的操纵子表达提供分级反应可能很重要。