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The kil-kor regulon of broad-host-range plasmid RK2: nucleotide sequence, polypeptide product, and expression of regulatory gene korC.

机译:宽宿主范围质粒RK2的kil-kor调节子:核苷酸序列,多肽产物和调控基因korC的表达。

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摘要

Broad-host-range plasmid RK2 encodes several kil operons (kilA, kilB, kilC, kilE) whose expression is potentially lethal to Escherichia coli host cells. The kil operons and the RK2 replication initiator gene (trfA) are coregulated by various combinations of kor genes (korA, korB, korC, korE). This regulatory network is called the kil-kor regulon. Presented here are studies on the structure, product, and expression of korC. Genetic mapping revealed the precise location of korC in a region near transposon Tn1. We determined the nucleotide sequence of this region and identified the korC structural gene by analysis of korC mutants. Sequence analysis predicts the korC product to be a polypeptide of 85 amino acids with a molecular mass of 9,150 daltons. The KorC polypeptide was identified in vivo by expressing wild-type and mutant korC alleles from a bacteriophage T7 RNA polymerase-dependent promoter. The predicted structure of KorC polypeptide has a net positive charge and a helix-turn-helix region similar to those of known DNA-binding proteins. These properties are consistent with the repressorlike function of KorC protein, and we discuss the evidence that KorA and KorC proteins act as corepressors in the control of the kilC and kilE operons. Finally, we show that korC is expressed from the bla promoters within the upstream transposon Tn1, suggesting that insertion of Tn1 interrupted a plasmid operon that may have originally included korC and kilC.
机译:宽宿主范围的质粒RK2编码了几种表达操纵子(kilA,kilB,kilC,kilE),其表达可能会对大肠杆菌宿主细胞致死。 Kil操纵子和RK2复制起始基因(trfA)由kor基因(korA,korB,korC,korE)的各种组合共调节。该监管网络称为“ kil-kor regulon”。这里介绍的是有关korC的结构,产物和表达的研究。遗传作图揭示了korC在转座子Tn1附近区域的精确位置。我们确定了该区域的核苷酸序列,并通过分析korC突变体鉴定了korC结构基因。序列分析预测korC产物是具有85个氨基酸的多肽,分子量为9,150道尔顿。通过表达来自噬菌体T7 RNA聚合酶依赖性启动子的野生型和突变korC等位基因,在体内鉴定了KorC多肽。 KorC多肽的预测结构具有净正电荷和与已知DNA结合蛋白相似的螺旋-转-螺旋区。这些特性与KorC蛋白的阻遏物功能一致,我们讨论了证据,证明KorA和KorC蛋白在控制kilC和kilE操纵子中充当共抑制因子。最后,我们显示korC是从上游转座子Tn1中的bla启动子表达的,这表明Tn1的插入打断了可能最初包含korC和kilC的质粒操纵子。

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