Grinter N J
Gene. 1983 Jan-Feb;21(1-2):133-43. doi: 10.1016/0378-1119(83)90155-5.
A system is described for the stable insertion of cloned DNA sequences into the chromosomes of Gram-negative bacteria. Two broad-host-range plasmids form the basis of the system: one (the "carrier") contains a transposable DNA sequence into which foreign DNA can be cloned; the second (the "helper") provides transposition functions in trans. Both plasmids can be readily transferred between Gram-negative bacteria by conjugation. Instability of the carrier allows enrichment for the products of transposition to the chromosome of the new host, following which the insertion can be stabilised by elimination of the helper. The system was successfully tested in Escherichia coli, Methylophilus methylotrophus and Pseudomonas aeruginosa, and the insertions were stable in each case (less than 0.02% loss per generation).
描述了一种用于将克隆的DNA序列稳定插入革兰氏阴性细菌染色体的系统。该系统基于两种广宿主范围的质粒:一种(“载体”)含有可克隆外源DNA的转座DNA序列;另一种(“辅助质粒”)提供反式转座功能。两种质粒都可以通过接合作用在革兰氏阴性细菌之间轻松转移。载体的不稳定性使得转座到新宿主染色体上的产物得以富集,之后通过去除辅助质粒可使插入稳定下来。该系统在大肠杆菌、嗜甲基甲基ophilus和铜绿假单胞菌中成功进行了测试,并且在每种情况下插入都是稳定的(每代损失小于0.02%)。