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IncI1质粒R64的trbABC区域的核苷酸序列及特征:转移区域内存在用于质粒维持的pnd基因。

Nucleotide sequence and characterization of the trbABC region of the IncI1 Plasmid R64: existence of the pnd gene for plasmid maintenance within the transfer region.

作者信息

Furuya N, Komano T

机构信息

Department of Biology, Tokyo Metropolitan University, Minamiohsawa, Hachioji, Japan.

出版信息

J Bacteriol. 1996 Mar;178(6):1491-7. doi: 10.1128/jb.178.6.1491-1497.1996.

Abstract

A 6.72-kb DNA sequence between the exc gene and the oriT operon within the transfer region of IncI1 plasmid R64 was sequenced and characterized. Three novel transfer genes, trbA, trbB, and trbC, were found in this region, along with the pnd gene responsible for plasmid maintenance. The trbABC genes appear to be organized into an operon located adjacent to the oriT operon in the opposite orientation. The trbA and trbC genes were shown to be indispensable for R64 plasmid transfer, while residual transfer activity was detected in the case of R64 derivatives carrying the trbB++ deletion mutation. The T7 RNA polymerase-promoter system revealed that the trbB gene produced a 43-kDa protein and the trbC gene produced an 85-kDa protein. The nucleotide sequence of the pnd gene is nearly identical to that of plasmid R483, indicating a function in plasmid maintenance. The plasmid stability test indicated that the mini-R64 derivatives with the pnd gene are more stably maintained in Escherichia coli cells under nonselective conditions than the mini-R64 derivatives without the pnd gene. It was also shown that the R64 transfer system itself is involved in plasmid stability to a certain degree. Deletion of the pnd gene from the tra+ mini-R64 derivative did not affect transfer frequency. DNA segments between the exc and trbA genes for IncI1 plasmids R64, Colb-P9, and R144 were compared in terms of their physical and genetic organization.

摘要

对 IncI1 质粒 R64 转移区域内 exc 基因与 oriT 操纵子之间的一段 6.72 kb 的 DNA 序列进行了测序和特征分析。在该区域发现了三个新的转移基因 trbA、trbB 和 trbC,以及负责质粒维持的 pnd 基因。trbABC 基因似乎被组织成一个与 oriT 操纵子相邻但方向相反的操纵子。trbA 和 trbC 基因被证明对 R64 质粒转移是不可或缺的,而在携带 trbB++缺失突变的 R64 衍生物中检测到了残余的转移活性。T7 RNA 聚合酶 - 启动子系统显示 trbB 基因产生一种 43 kDa 的蛋白质,trbC 基因产生一种 85 kDa 的蛋白质。pnd 基因的核苷酸序列与质粒 R483 的几乎相同,表明其在质粒维持中的功能。质粒稳定性测试表明,带有 pnd 基因的 mini - R64 衍生物在非选择性条件下比没有 pnd 基因的 mini - R64 衍生物在大肠杆菌细胞中更稳定地维持。还表明 R64 转移系统本身在一定程度上参与了质粒稳定性。从 tra + mini - R64 衍生物中缺失 pnd 基因不影响转移频率。对 IncI1 质粒 R64、Colb - P9 和 R144 的 exc 与 trbA 基因之间的 DNA 片段在物理和遗传组织方面进行了比较。

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