Simon R, Hötte B, Klauke B, Kosier B
Lehrstuhl für Genetik, Fakultät für Biologie, Universität Bielefeld, Federal Republic of Germany.
J Bacteriol. 1991 Feb;173(4):1502-8. doi: 10.1128/jb.173.4.1502-1508.1991.
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.
基于一种源自RSF1010的广宿主范围载体,构建了三种不同的系统,可从革兰氏阴性细菌中阳性检测和分离插入序列(IS)元件。载体pSUP104-pheS、pSUP104-rpsL和pSUP104-sac已成功应用于多种根瘤菌菌株和野油菜黄单胞菌。分离并鉴定了20多种不同的IS元件。来自苜蓿根瘤菌的16种IS元件进一步用于通过杂交鉴定各种苜蓿根瘤菌菌株。每个菌株的杂交结果模式都不同,给出了每个菌株清晰明确的IS指纹图谱。这些IS指纹图谱可用于快速、明确地鉴定和表征苜蓿根瘤菌菌株,因为它们被证明相对稳定。当比较给定菌株的IS指纹图谱时,发现一些IS元件是相同的。这种IS指纹图谱方法还可以确定IS元件是否相同、相关或不同。