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通过转座子诱变对广宿主范围质粒RK2的trfA区域进行分析并鉴定多肽产物。

Analysis of the trfA region of broad host-range plasmid RK2 by transposon mutagenesis and identification of polypeptide products.

作者信息

Shingler V, Thomas C M

出版信息

J Mol Biol. 1984 May 25;175(3):229-49. doi: 10.1016/0022-2836(84)90346-2.

Abstract

Broad host-range plasmid RK2 is a member of the Escherichia coli incompatibility group P. Unlike most other groups of plasmids, members of the P group are capable of efficient transfer between and maintenance in most gram-negative bacterial species. It is of interest whether this broad host-range results from differences between the mechanism of replication of broad and narrow host-range plasmids. The regions of RK2 required for replication in E. coli have previously been defined as an origin of vegetative replication, oriVRK2 , and a gene, trfA , specifying a positively required trans-acting product. In this study Tn1723 transposon insertions have been used to map the trfA gene and determine its functional gene product. The Tn1723 insertions define the outer limits of the gene, a promoter region, a "leader" region not essential for trfA activity and a coding region. Three polypeptides of 13 X 10(3), 43 X 10(3) and 32 X 10(3) molecular weight are produced from this region and the production of a 32 X 10(3) Mr polypeptide is shown to be correlated with trfA activity in E. coli. Analysis of polypeptides produced from transposon insertion derivatives in which all but 35 base-pairs of inserted DNA is deleted, along with the effect of these insertions on trfA activity, suggest that the 43 X 10(3) and 32 X 10(3) Mr polypeptide coding sequences overlap in the same reading frame and that all three polypeptides (13 X 10(3), 32 X 10(3) and 43 X 10(3) Mr) may be translated from the same initial transcript.

摘要

广宿主范围质粒RK2是大肠杆菌不相容群P的成员。与大多数其他质粒群不同,P群成员能够在大多数革兰氏阴性细菌物种之间高效转移并维持。这种广宿主范围是否源于广宿主范围和窄宿主范围质粒复制机制的差异,这一点很值得研究。此前已确定RK2在大肠杆菌中复制所需的区域为营养复制起点oriVRK2和一个基因trfA,该基因指定了一种正向所需的反式作用产物。在本研究中,Tn1723转座子插入已被用于绘制trfA基因图谱并确定其功能性基因产物。Tn1723插入确定了该基因的外部界限、一个启动子区域、一个对trfA活性非必需的“前导”区域和一个编码区域。从该区域产生了分子量分别为13×10³、43×10³和32×10³的三种多肽,并且已证明32×10³分子量多肽的产生与trfA在大肠杆菌中的活性相关。对转座子插入衍生物产生的多肽进行分析,其中除35个碱基对外的所有插入DNA均被删除,以及这些插入对trfA活性的影响,表明43×10³和32×10³分子量多肽的编码序列在同一阅读框中重叠,并且所有三种多肽(13×10³、32×10³和43×10³分子量)可能从同一初始转录本翻译而来。

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