Casey J, Daly C, Fitzgerald G F
Food Microbiology Department, University College, Cork, Ireland.
Appl Environ Microbiol. 1991 Sep;57(9):2677-82. doi: 10.1128/aem.57.9.2677-2682.1991.
Integration of pCI192, a pBR322-derived vector plasmid containing homology to the chromosomally located conjugative transposon Tn919 was observed in two strains that harbor Tn919, namely, Enterococcus faecalis GF590 and Lactococcus lactis subsp. lactis CH919. Hybridization analysis indicated that single-copy integration of the plasmid had occurred at low frequency. The Tn919::plasmid structure was conjugated from an E. faecalis donor to a L. lactis recipient, although at lower frequencies than was Tn919. Segregation of the tetracycline and chloramphenicol resistance markers during conjugation was observed. The integration strategy described allows for DNA manipulations to be performed in an easily manipulated model host strain with the subsequent transfer of integrated structures by conjugation to any strain capable of receiving Tn919. The results indicate that homologous recombination events may be used to introduce plasmid-encoded genes to the lactococcal chromosome.
在两株携带Tn919的菌株中观察到了pCI192的整合,pCI192是一种源自pBR322的载体质粒,与染色体定位的接合转座子Tn919具有同源性,这两株菌分别是粪肠球菌GF590和乳酸乳球菌乳酸亚种CH919。杂交分析表明,质粒的单拷贝整合以低频率发生。尽管Tn919::质粒结构从粪肠球菌供体接合到乳酸乳球菌受体的频率低于Tn919,但仍能发生。在接合过程中观察到了四环素和氯霉素抗性标记的分离。所述的整合策略允许在易于操作的模式宿主菌株中进行DNA操作,随后通过接合将整合结构转移到任何能够接收Tn919的菌株中。结果表明,同源重组事件可用于将质粒编码的基因引入乳球菌染色体。