Kanaya S, Crouch R J
Proc Natl Acad Sci U S A. 1984 Jun;81(11):3447-51. doi: 10.1073/pnas.81.11.3447.
We have determined that a functional gene coding for ribonuclease H seems to be essential for cell growth in Escherichia coli. A strain was made with two copies of the rnh gene by lysogenizing an E. coli strain with a lambda phage bearing a copy of the rnh gene. Inactivation of one of the two copies of the rnh gene was accomplished by transformation with a linear DNA molecule that had the gene for chloramphenicol acetyltransferase inserted near the middle of the rnh gene. In recombinants that had an inactive gene replacing the normal chromosomal rnh gene, the lambda rnh prophage supplies an intact functional copy of the rnh gene. Curing the cells of the lambda rnh prophage left the cell with an inactive rnh gene and resulted in cell death. An intact functional rnh gene provided on a plasmid permits normal curing, and cured survivors were readily obtained. The technique described is probably generally applicable for assessing the requirement for other E. coli genes.
我们已经确定,编码核糖核酸酶H的功能基因似乎对大肠杆菌的细胞生长至关重要。通过用携带rnh基因拷贝的λ噬菌体对大肠杆菌菌株进行溶原化,构建了一个含有两个rnh基因拷贝的菌株。通过用线性DNA分子转化来使两个rnh基因拷贝中的一个失活,该线性DNA分子在rnh基因中间附近插入了氯霉素乙酰转移酶基因。在具有失活基因取代正常染色体rnh基因的重组体中,λrnh原噬菌体提供rnh基因的完整功能拷贝。去除细胞中的λrnh原噬菌体后,细胞只剩下一个失活的rnh基因,并导致细胞死亡。在质粒上提供完整的功能性rnh基因可实现正常的去除,并且很容易获得去除后的存活菌株。所描述的技术可能普遍适用于评估对其他大肠杆菌基因的需求。