Klier A F, Kunst F, Rapoport G
Nucleic Acids Res. 1979 Oct 25;7(4):997-1010. doi: 10.1093/nar/7.4.997.
A library of B. thuringiensis DNA has been prepared by using the plasmid pBR322 as a cloning vehicle and E. coli as a host cell. By screening this collection with specific probes, 17 clones were identified whose hybrid plasmids contain rRNA genes of B. thuringiensis. Several of these plasmids have been mapped with restriction endonucleases and by DNA-RNA hybridization. By using maps of overlapping fragments, we have been able to establish an overall map of the ribosomal gene cluster.
通过使用质粒pBR322作为克隆载体以及大肠杆菌作为宿主细胞,构建了苏云金芽孢杆菌DNA文库。通过用特异性探针筛选该文库,鉴定出了17个克隆,其杂交质粒含有苏云金芽孢杆菌的rRNA基因。其中几个质粒已用限制性内切酶进行了图谱绘制,并通过DNA-RNA杂交进行了分析。通过使用重叠片段的图谱,我们得以构建核糖体基因簇的总图。