首页> 外文期刊>Applied and Environmental Microbiology >Characterization, distribution, and localization of ISRl2, and insertion sequence element isolated from Rhizobium leguminosarum bv. viciae.
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Characterization, distribution, and localization of ISRl2, and insertion sequence element isolated from Rhizobium leguminosarum bv. viciae.

机译:ISR12的鉴定,分布和定位,以及从豆科根瘤菌中分离的插入序列元件。蚕豆

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An insertion sequence (IS) element, ISR12, from Rhizobium leguminosarum bv. viciae strain MSDJ4184 was isolated by insertional inactivation of the sacRB gene of pSUP104-sac, which allows positive selection. ISRl2 is 932 bp long, is flanked by 17-bp imperfect terminal inverted repeats, and generated a 3-bp target site duplication. ISRl2 was found to be 63 to 77% homologous to insertion elements of the IS5 group of the IS4 superfamily. A probe incorporating a full-length copy of ISRl2 was used to screen genomic DNAs from a collection of strains and from two field populations of R. leguminosarum to detect and estimate the copy numbers of homologous sequences. Among the collection of 63 strains representing the different species and genera of members of the family Rhizobiaceae, homology to ISRl2 was found within strains belonging to Sinorhizobium meliloti and S. fredii; within four of the six recognized Rhizobium species. R. leguminosarum, R. tropici, R. etli, and R. galegae; and within Rhizobium sp. (Phaseolus) genomic species 2. The apparent copy numbers of ISRl2 varied from one to eight. Among 139 isolates of R. leguminosarum from two field populations, homology to ISRl2 was detected in 91% of the isolates from one site and in 17% from the other. Analysis of the 95 isolates that hybridize to ISRl2 revealed a total of 20 distinct hybridization patterns composed of one to three bands. Probing blots of Eckhardt gels showed that sequences with homology to ISRl2 may be found on plasmids or the chromosome. Analysis of their genomic distribution demonstrated relationships and diversity among the R. leguminosarum isolates tested.
机译:来自豆根瘤菌bv的插入序列(IS)元件ISR12。通过插入失活pSUP104-sac的sacRB基因分离了蚕豆菌株MSDJ4184,从而可以进行阳性选择。 ISR12长932 bp,侧翼是17 bp不完美的末端反向重复序列,并产生了3 bp的目标位点重复。发现ISR12与IS4超家族的IS5基团的插入元件同源63-77%。使用掺入有ISRl2全长拷贝的探针,从一系列菌株和两个豆科植物豆科实地种群中筛选基因组DNA,以检测和估计同源序列的拷贝数。在代表根瘤菌科成员的不同物种和属的63个菌株的集合中,与ISRl2的同源性被发现于苜蓿中华根瘤菌和弗氏链球菌的菌株中。六个公认的根瘤菌物种中的四个。 R. leguminosarum,R。tropici,R。etli和R. galegae;并且在根瘤菌属内。 (菜豆)基因组物种2. ISR12的表观拷贝数从1到8不等。在来自两个田间种群的139个豆科菌的分离物中,与ISRl2的同源性在一个站点的91%的分离株中和在另一站点的17%的分离株中被检测到。对与ISR12杂交的95个分离株的分析显示,共有20种不同的杂交模式,由一到三个条带组成。 Eckhardt凝胶的探测印迹表明,与ISR12同源的序列可能在质粒或染色体上发现。对它们的基因组分布进行分析,证明了所测试的豆科菌分离株之间的关系和多样性。

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