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泛宿主性质粒RK2的kilA操纵子:利用转导噬菌体(λpklaA-1)确定致死性klaA基因对大肠杆菌细胞的影响。

The kilA operon of promiscuous plasmid RK2: the use of a transducing phage (lambda pklaA-1) to determine the effects of the lethal klaA gene on Escherichia coli cells.

作者信息

Saltman L H, Kim K S, Figurski D H

机构信息

Department of Microbiology, College of Physicians and Surgeons, Columbia University, New York, New York 10032.

出版信息

Mol Microbiol. 1991 Nov;5(11):2673-83. doi: 10.1111/j.1365-2958.1991.tb01976.x.

Abstract

The kil-kor regulon of promiscuous plasmid RK2 includes the replication initiator gene trfA and several potentially host-lethal kil loci (kilA, kilB, kilC, kilE), whose functions may be involved in plasmid maintenance or broad host range. The kilA locus consists of a single operon of three genes (klaA, klaB, klaC), each of which is lethal when expressed from the klaA promoter in the absence of repressors encoded by korA and korB. In this study, we examined the effects of the unregulated klaA gene on the host cell. Bacteriophage lambda was used to construct a transducing phage (lambda pklaA-1) that allows efficient introduction of the klaA gene into Escherichia coli. Cells lacking korA and korB (to allow uncontrolled expression of klaA) and expressing lambda repressor (to prevent phage lytic growth) are killed by lambda pklaA-1. Cell death is dependent on the klaA structural gene, independent of the SOS system of the host, and is prevented by the presence of korA and korB. lambda pklaA-1 was used to synchronously infect cells lacking korA and korB to determine the effects of klaA on the cells over time. The earliest effects, visible at two hours post-infection, are inhibition of growth of the culture, formation of elongated cells, and striking changes in the appearance of the outer membrane. After four to five hours, the viability of the culture declined sharply and macromolecular synthesis ceased. The distinct class of early events is consistent with the hypothesis that the KlaA polypeptide interacts with a specific target in the host cell.

摘要

杂乱质粒RK2的kil - kor调节子包括复制起始基因trfA和几个潜在的宿主致死性kil位点(kilA、kilB、kilC、kilE),其功能可能与质粒维持或广泛宿主范围有关。kilA位点由一个包含三个基因的单一操纵子(klaA、klaB、klaC)组成,在没有由korA和korB编码的阻遏物的情况下,从klaA启动子表达时,每个基因都是致死性的。在本研究中,我们研究了不受调控的klaA基因对宿主细胞的影响。噬菌体λ被用于构建一种转导噬菌体(λpklaA - 1),该噬菌体能够有效地将klaA基因导入大肠杆菌。缺乏korA和korB(以允许klaA不受控制地表达)并表达λ阻遏物(以防止噬菌体裂解生长)的细胞会被λpklaA - 1杀死。细胞死亡依赖于klaA结构基因,独立于宿主的SOS系统,并且korA和korB的存在可阻止细胞死亡。λpklaA - 1被用于同步感染缺乏korA和korB的细胞,以确定随着时间推移klaA对细胞的影响。最早在感染后两小时可见的影响是培养物生长受到抑制、细胞伸长以及外膜外观发生显著变化。四到五小时后,培养物的活力急剧下降,大分子合成停止。这一独特的早期事件类别与KlaA多肽与宿主细胞中的特定靶标相互作用的假设一致。

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