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Isolation and characterization of insertion sequence elements from gram-negative bacteria by using new broad-host-range positive selection vectors.

机译:通过使用新型的广泛宿主阳性选择载体从革兰氏阴性细菌中分离和鉴定插入序列元件。

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摘要

On the basis of an RSF1010-derived broad-host-range vector, three different systems which enable positive detection and isolation of insertion sequence (IS) elements from gram-negative bacteria were constructed. Vectors pSUP104-pheS, pSUP104-rpsL, and pSUP104-sac were used successfully in a number of Rhizobium strains and in Xanthomonas campestris. More than 20 different IS elements were isolated and characterized. The 16 IS elements from Rhizobium meliloti were further used to characterize various R. meliloti strains by hybridization. The resulting hybridization patterns were different for every strain and gave a clear and definite IS fingerprint of each strain. These IS fingerprints can be used to identify and characterize R. meliloti strains rapidly and unequivocally, as they proved to be relatively stable. Some of the IS elements were found to be identical when the IS fingerprints from a given strain were compared. This method of IS fingerprinting can also establish whether IS elements are the same, related, or different.
机译:在源自RSF1010的广泛宿主载体的基础上,构建了三个不同的系统,这些系统可以对革兰氏阴性细菌进行插入序列(IS)元素的阳性检测和分离。载体pSUP104-pheS,pSUP104-rpsL和pSUP104-sac已成功用于许多根瘤菌菌株和油菜黄单胞菌中。分离和表征了20多种不同的IS元素。来自苜蓿根瘤菌的16个IS元素通过杂交进一步用于表征多种苜蓿根瘤菌菌株。每种菌株产生的杂交模式是不同的,并且给出了每种菌株清晰明确的IS指纹。这些IS指纹可以证明是相对稳定的,因此可用于快速,明确地鉴定和鉴定苜蓿根瘤菌菌株。当比较来自给定菌株的IS指纹时,发现某些IS元素是相同的。 IS指纹识别的这种方法还可以确定IS元素是相同,相关还是不同。

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