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丁香假单胞菌丁香致病变种中密切相关的抗铜和抗链霉素质粒的分子分析

Molecular analysis of closely related copper- and streptomycin-resistance plasmids in Pseudomonas syringae pv. syringae.

作者信息

Sundin G W, Bender C L

机构信息

Department of Plant Pathology, Oklahoma State University, Stillwater 74078, USA.

出版信息

Plasmid. 1996 Mar;35(2):98-107. doi: 10.1006/plas.1996.0012.

Abstract

The genetic relationship of a group of copper (Cur) and streptomycin (Smr) resistance plasmids and their Pseudomonas syringae pv. syringae hosts was examined. Each of these plasmids contained sequences homologous to the oriV and par sequences from pOSU900, a cryptic P. syringae pv. syringae plasmid. Analysis of restriction digest patterns of plasmid DNA indicated that the plasmids could be clustered into four groups; two of the groups contained multiple members which differed by only a few fragments. An analysis of the host P. syringae genotypes using the arbitrarily primed PCR technique and genomic DNA indicated that the host strains could be placed in groups similar to those resulting from analysis of plasmid DNA. Southern hybridization analyses of plasmid DNA indicated that each Smr plasmid contained sequences homologous to probes specific for the strA-strB Smr genes and the transposase and resolvase genes from Tn5393. All plasmids hybridized to two additional probes derived from P. syringae plasmid DNA, but none of the plasmids contained IS51 or IS801 sequences. Furthermore, Tn5393 was mobilized, presumably by transposition, between the incompatible plasmids pPSR5 and pPSR4 in P. syringae pv. syringae FF5. The variation in molecular structure of the closely related plasmids in this study is similar to that observed with antibiotic-resistance plasmids from clinical bacteria.

摘要

研究了一组抗铜(Cur)和抗链霉素(Smr)质粒与其丁香假单胞菌丁香致病变种宿主之间的遗传关系。这些质粒中的每一个都含有与来自隐匿性丁香假单胞菌丁香致病变种质粒pOSU900的oriV和par序列同源的序列。质粒DNA的限制性消化图谱分析表明,这些质粒可分为四组;其中两组包含多个成员,它们之间仅相差几个片段。使用任意引物PCR技术和基因组DNA对宿主丁香假单胞菌基因型进行分析表明,宿主菌株可分为与质粒DNA分析结果相似的组。质粒DNA的Southern杂交分析表明,每个Smr质粒都含有与针对strA-strB Smr基因以及来自Tn5393的转座酶和解离酶基因的特异性探针同源的序列。所有质粒都与源自丁香假单胞菌质粒DNA的另外两个探针杂交,但没有一个质粒含有IS51或IS801序列。此外,Tn5393可能通过转座在丁香假单胞菌丁香致病变种FF5的不相容质粒pPSR5和pPSR4之间移动。本研究中密切相关质粒的分子结构变化与临床细菌的抗生素抗性质粒所观察到的变化相似。

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