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广宿主范围质粒RK2的trfA基因转录方向的遗传证据。

Genetic evidence for the direction of transcription of the trfA gene of broad host range plasmid RK2.

作者信息

Thomas C M

出版信息

J Gen Microbiol. 1984 Jul;130(7):1641-50. doi: 10.1099/00221287-130-7-1641.

Abstract

For replication of broad host range plasmid RK2 in Escherichia coli two regions of the plasmid genome are essential, oriV RK2 between 12.0 and 12.7 kb on the genome (defined clockwise from the unique EcoRI site) and trfA, located between 16.0 and 17.4 kb, which provides a trans-acting product necessary for oriV RK2 function. The properties of an insertion mutant of a mini-RK2/ColE1 hybrid plasmid suggest that the trfA promoter lies clockwise from the 17.4 kb RK2 coordinate. Fusion of the trfA gene lacking its normal promoter to the E. coli trpE gene in a hybrid plasmid confirmed that trfA is transcribed anticlockwise, towards the Tcr gene of RK2. Repression of trpE promoter activity in these fusions showed that replication of an RK2 replicon can be regulated by varying the level of trfA gene expression. The results also indicate the presence of a transcription unit running anticlockwise through the trfB region located between 54.0 and 56.0 kb on the RK2 genome.

摘要

对于广宿主范围质粒RK2在大肠杆菌中的复制,质粒基因组的两个区域至关重要,即基因组上12.0至12.7 kb之间的oriV RK2(从唯一的EcoRI位点顺时针定义)和位于16.0至17.4 kb之间的trfA,它提供oriV RK2功能所需的反式作用产物。一个mini-RK2/ColE1杂种质粒插入突变体的特性表明,trfA启动子位于17.4 kb RK2坐标的顺时针方向。在杂种质粒中将缺乏正常启动子的trfA基因与大肠杆菌trpE基因融合,证实trfA是逆时针转录的,朝向RK2的Tcr基因。这些融合体中trpE启动子活性的抑制表明,RK2复制子的复制可通过改变trfA基因表达水平来调控。结果还表明,存在一个逆时针穿过RK2基因组上54.0至56.0 kb之间trfB区域的转录单元。

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