Heath J D, Perkins J D, Sharma B, Weinstock G M
Department of Biochemistry and Molecular Biology, University of Texas Medical School, Houston 77225.
J Bacteriol. 1992 Jan;174(2):558-67. doi: 10.1128/jb.174.2.558-567.1992.
Several approaches were used to construct a complete NotI restriction enzyme cleavage map of the genome of Escherichia coli MG1655. The approaches included use of transposable element insertions that created auxotrophic mutations and introduced a NotI site into the genome, hybridization of NotI fragments to the ordered lambda library constructed by Kohara et al. (BioTechniques 10:474-477, 1991), Southern blotting of NotI digests with cloned genes as probes, and analysis of the known E. coli DNA sequence for NotI sites. In all, 22 NotI cleavage sites were mapped along with 26 transposon insertions. These sites were localized to clones in the lambda library and, when possible, sequenced genes. The map was compared with that of strain EMG2, a wild-type E. coli K-12 strain, and several differences were found, including a region of about 600 kb with an altered restriction pattern and an additional fragment in MG1655. Comparison of MG1655 with other strains revealed minor differences but indicated that this map was representative of that for many commonly used E. coli K-12 strains.
采用了几种方法来构建大肠杆菌MG1655基因组的完整NotI限制性内切酶切割图谱。这些方法包括利用产生营养缺陷型突变并将NotI位点引入基因组的转座子插入、将NotI片段与Kohara等人构建的有序λ文库(《生物技术》10:474 - 477, 1991)进行杂交、以克隆基因为探针进行NotI酶切产物的Southern印迹分析以及分析大肠杆菌已知DNA序列中的NotI位点。总共确定了22个NotI切割位点以及26个转座子插入位点。这些位点定位到了λ文库中的克隆上,并在可能的情况下对相关基因进行了测序。将该图谱与野生型大肠杆菌K - 12菌株EMG2的图谱进行比较,发现了一些差异,包括约600 kb区域的限制性图谱改变以及MG1655中有一个额外的片段。将MG1655与其他菌株进行比较揭示了一些细微差异,但表明该图谱代表了许多常用大肠杆菌K - 12菌株的图谱。