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IncI1 质粒 R64 的 traABCD 区域的核苷酸序列及特征

Nucleotide sequence and characterization of the traABCD region of IncI1 plasmid R64.

作者信息

Kim S R, Funayama N, Komano T

机构信息

Department of Biology, Tokyo Metropolitan University, Japan.

出版信息

J Bacteriol. 1993 Aug;175(16):5035-42. doi: 10.1128/jb.175.16.5035-5042.1993.

Abstract

A 3.6-kb BglII-SmaI segment of the transfer region of IncI1 plasmid R64drd-11 was sequenced and characterized. Analysis of the DNA sequence indicated the presence of four genes, traA, traB, traC, and traD, in this region. The expression of the traB, traC, and traD genes was examined by maxicell experiments and that of the traA gene was examined by constructing the traA-lacZ fusion gene. The introduction of frameshift mutations into the four genes indicated that the traB and traC genes are essential for conjugal transfer in liquid medium and on a solid surface. Both were also required for the formation of the thin pilus, which is the receptor for phages I alpha and PR64FS. Upstream of the traA gene, a promoter sequence for sigma 70 of E. coli RNA polymerase was identified by S1 nuclease mapping and primer extension experiments.

摘要

对IncI1质粒R64drd - 11转移区域的一段3.6 kb BglII - SmaI片段进行了测序和特征分析。DNA序列分析表明该区域存在四个基因,即traA、traB、traC和traD。通过大细胞实验检测了traB、traC和traD基因的表达,并通过构建traA - lacZ融合基因检测了traA基因的表达。在这四个基因中引入移码突变表明,traB和traC基因对于在液体培养基和固体表面的接合转移至关重要。它们也是形成细菌毛所必需的,细菌毛是噬菌体Iα和PR64FS的受体。在traA基因上游,通过S1核酸酶作图和引物延伸实验鉴定出大肠杆菌RNA聚合酶σ70的启动子序列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a6/204969/6c67262e466e/jbacter00058-0105-a.jpg

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