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恶臭假单胞菌R-prime质粒的分离与鉴定

Isolation and characterization of Pseudomonas putida R-prime plasmids.

作者信息

Bray R, Strom D, Barton J, Dean H F, Morgan A F

机构信息

Department of Genetics, Monash University, Clayton, Victoria, Australia.

出版信息

J Gen Microbiol. 1987 Mar;133(3):683-90. doi: 10.1099/00221287-133-3-683.

Abstract

A number of enhanced chromosome mobilizing (ECM) plasmids derived from the wide host range plasmid R68 have been used to construct R-prime plasmids carrying a maximum of two map minutes of the Pseudomonas putida PPN chromosome, using Pseudomonas aeruginosa PAO as the recipient. For one ECM plasmid, pMO61, the ability to form R-primes did not correlate with the ability to mobilize chromosomes in intrastrain crosses, suggesting that different mechanisms are involved. Physical analysis of one R-prime showed that 3.5 kb of chromosomal DNA had been inserted between the tandem IS21 sequences carried by the parent ECM plasmid.

摘要

一些源自广宿主范围质粒R68的增强型染色体动员(ECM)质粒已被用于构建携带恶臭假单胞菌PPN染色体最多两分钟图谱的R-prime质粒,使用铜绿假单胞菌PAO作为受体。对于一种ECM质粒pMO61,形成R-prime的能力与在菌株内杂交中动员染色体的能力不相关,这表明涉及不同的机制。对一种R-prime的物理分析表明,3.5 kb的染色体DNA已插入到亲本ECM质粒携带的串联IS21序列之间。

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