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首页> 外文期刊>Plasmid: An International Journal Devoted to Extrachromosomal Gene Systems >The central lysine in the P-loop motif of the Escherichia coli DnaA protein is essential for initiating DNA replication from the chromosomal origin, oriC, and the F factor origin, oriS, but is dispensable for initiation from the P1 plasmid origin, or
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The central lysine in the P-loop motif of the Escherichia coli DnaA protein is essential for initiating DNA replication from the chromosomal origin, oriC, and the F factor origin, oriS, but is dispensable for initiation from the P1 plasmid origin, or

机译:大肠杆菌DnaA蛋白P环基序中的中央赖氨酸对于启动从染色体来源oriC和F因子来源oriS的DNA复制是必不可少的,但对于从P1质粒来源的起始是必需的,或者

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The Escherichia coli DnaA protein is essential for initiation of DNA replication from the chromosomal origin, oriC, and from certain plasmid origins such as oriR of P1, oriS of F, and ori of pSCS101. The DnaA protein binds ATP with high affinity and contains a P-loop motif assumed to be the binding site. Three mutations in the E. coli dnaA gene were constructed by oligonucleotide-directed mutagenesis that changed amino acids in the P-loop. A DnaA protein, K178T, in which the central lysine was changed to the smaller amino acid threonine, was able to initiate DNA replication from P1 oriR, but was unable to initiate replication from E. coli oriC or F oriS in vivo. Mutant and wild-type DnaA proteins were overexpressed, partially purified, and tested for replication activity in vitro. The K178T DnaA protein could initiate replication from oriR, although with a decreased activity compared to the wild-type DnaA protein. No replication activity was detected for this mutant protein from oriC. The different responses of the oriR and oriC replicons to the K178T DnaA protein indicate that the role of DnaA is different in the two systems.
机译:大肠杆菌DnaA蛋白对于从染色体来源oriC和某些质粒来源(例如P1的oriR,F的oriS和pSCS101的ori)启动DNA复制至关重要。 DnaA蛋白以高亲和力结合ATP,并包含一个P环基序(假定为结合位点)。大肠杆菌dnaA基因的三个突变是通过寡核苷酸定向诱变构建的,该突变改变了P环中的氨基酸。 DnaA蛋白K178T(其中的中央赖氨酸变为较小的氨基酸苏氨酸)能够从P1 oriR启动DNA复制,但无法在体内从大肠杆菌oriC或F oriS启动复制。突变和野生型DnaA蛋白被过表达,部分纯化并在体外测试其复制活性。 K178T DnaA蛋白可以从oriR启动复制,尽管与野生型DnaA蛋白相比活性降低。没有检测到来自oriC的该突变蛋白的复制活性。 oriR和oriC复制子对K178T DnaA蛋白的不同反应表明,DnaA在两个系统中的作用不同。

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