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Effect of Different Concentrations of H-NS Protein on Chromosome Replication and the Cell Cycle in Escherichia coli

机译:不同浓度的H-NS蛋白对大肠杆菌中染色体复制和细胞周期的影响

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Flow cytometric analysis showed that the hns205 and hns206 mutants, lacking the abundant nucleoid-associated protein H-NS, have decreased origin concentration, as well as a low number of origins per cell (ploidy). The most striking observation was that the low ploidy was due to a very short replication time, e.g., at 30°C it was halved compared to that of the hns+ strain. The decreased origin concentration was not caused by a decreased dnaA gene expression, and the hns206 mutant had normal DnaA protein concentrations. The replication phenotypes of the hns206 mutant were independent of RpoS. Cells overproducing H-NS from a LacI-controlled plasmid had a normal origin concentration, indicating that H-NS is not controlling initiation. A wild-type H-NS concentration is, however, required to obtain a wild-type origin concentration, since cells with an intermediate H-NS concentration had an intermediate origin concentration. Two lines of evidence point to an indirect effect of H-NS on initiation. First, H-NS did not show high-affinity binding to any part of oriC, and H-NS had no effect on transcription entering oriC from the mioC promoter. Second, in a shift experiment with the hns206 mutant, when H-NS protein was induced to wild-type levels within 10 min, it took more than one generation before the origin concentration started to increase.
机译:流式细胞仪分析表明,缺少大量与核苷酸相关的蛋白H-NS的 hns205 hns206 突变体,其起源浓度降低,且每细胞(倍性)。最惊人的观察结果是低倍性是由于很短的复制时间所致,例如,在30°C下,与 hns + 菌株相比,复制倍数降低了一半。降低的起源浓度不是由 dnaA 基因表达降低引起的,并且 hns206 突变体具有正常的DnaA蛋白浓度。 hns206 突变体的复制表型独立于RpoS。从LacI控制的质粒中过量产生H-NS的细胞具有正常的起始浓度,表明H-NS不控制起始。然而,由于具有中等H-NS浓度的细胞具有中等起源浓度,因此需要野生型H-NS浓度以获得野生型起源浓度。有两条证据表明H-NS对引发有间接影响。首先,H-NS没有显示与 oriC 的任何部分的高亲和力结合,H-NS对从 mioC oriC 进入的转录没有影响。 / em>启动子。其次,在使用 hns206 突变体的转移实验中,当H-NS蛋白在10分钟内被诱导为野生型水平时,花了不止一个世代才开始增加起始浓度。

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