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对在pQF系列广宿主质粒中发现的pRO1600 OriR区域进行缺失、转座子诱变及序列分析。

Deletion and transposon mutagenesis and sequence analysis of the pRO1600 OriR region found in the broad-host-range plasmids of the pQF series.

作者信息

Jansons I, Touchie G, Sharp R, Almquist K, Farinha M A, Lam J S, Kropinski A M

机构信息

Department of Microbiology and Immunology, Queen's University, Kingston, Ontario, Canada.

出版信息

Plasmid. 1994 May;31(3):265-74. doi: 10.1006/plas.1994.1028.

Abstract

The nucleotide sequence of the replicative origin (OriR) region of the small cryptic broad-host-range plasmid, pRO1600, which forms the basis of a number of useful cloning vectors has been determined. In addition it has been subjected to Tn5 mutagenesis, deletion analysis, and subcloning in order to define the regions essential for replication in Pseudomonas aeruginosa. The sequence (1894 bp) contains a fragment derived from transposon Tn1. The OriR region is structurally related to other replication (Rep) protein-dependent origins in that it has an A-T-rich region upstream of four 17-bp direct repeats (iterons) which presumably function in initiator protein binding. The sequence also contains a DNA-A-binding site and an open reading frame which could encode a basic (pI 10.6) 25,343-Da Rep protein with homology to RepA from the Neisseria gonorrhoeae beta-lactamase plasmid pFA3. The possible evolutionary origin of this plasmid in P. aeruginosa (RP1) is discussed.

摘要

小型隐蔽型广宿主范围质粒pRO1600的复制起点(OriR)区域的核苷酸序列已被确定,该质粒是许多有用的克隆载体的基础。此外,为了确定在铜绿假单胞菌中复制所必需的区域,它还进行了Tn5诱变、缺失分析和亚克隆。该序列(1894 bp)包含一个来自转座子Tn1的片段。OriR区域在结构上与其他依赖复制(Rep)蛋白的起点相关,因为它在四个17 bp直接重复序列(迭代子)上游有一个富含A-T的区域,推测该区域在起始蛋白结合中起作用。该序列还包含一个DNA-A结合位点和一个开放阅读框,该开放阅读框可以编码一个碱性(pI 10.6)、25343 Da的Rep蛋白,与淋病奈瑟菌β-内酰胺酶质粒pFA3的RepA具有同源性。讨论了该质粒在铜绿假单胞菌(RP1)中可能的进化起源。

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