Lichens-Park A, Smith C L, Syvanen M
Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts 02115.
J Bacteriol. 1990 May;172(5):2201-8. doi: 10.1128/jb.172.5.2201-2208.1990.
Bacteriophage lambda missing its chromosomal attachment site will integrate into recA+ Escherichia coli K-12 and C at the sites of cryptic prophages. The specific regions in which these recombination events occur were identified in both lambda and the bacterial chromosomes. A NotI restriction site on the prophage allowed its physical mapping. This allowed us to identify the locations of Rac, Qin, and Qsr' cryptic prophages on the NotI map of E. coli K-12 and, by analogy, to identify the cryptic prophage in E. coli C as Qin. No new cryptic prophages were detected in E. coli K-12.
缺失染色体附着位点的噬菌体λ将整合到recA⁺大肠杆菌K - 12和C的隐蔽原噬菌体位点。在λ和细菌染色体中都鉴定出了这些重组事件发生的特定区域。原噬菌体上的一个NotI限制位点使其能够进行物理图谱绘制。这使我们能够在大肠杆菌K - 12的NotI图谱上确定Rac、Qin和Qsr'隐蔽原噬菌体的位置,并通过类推,将大肠杆菌C中的隐蔽原噬菌体鉴定为Qin。在大肠杆菌K - 12中未检测到新的隐蔽原噬菌体。