Domenico P, Gotschlich E C, Cunha B A
Infectious Disease Division, Winthrop-University Hospital, Mineola, New York 11501.
Infection. 1990 May-Jun;18(3):181-5. doi: 10.1007/BF01642111.
Transfer of plasmid DNA from penicillinase-producing Neisseria gonorrhoeae to Escherichia coli produced relatively small colonies that became pigmented in the presence of the dye, congo red. Mutations to large, non-pigmented colonies were frequent, and were the result of a variety of alterations in these plasmids. Miniplasmid formation was the major alteration that led to non-pigmented colonies. However, deletions in any of three putative replication regions resulted in non-pigmented colonies. These altered plasmids mediated significantly less beta-lactamase production than that of the parent plasmid. A new origin of replication was discovered and mapped within the miniplasmid. This origin was responsible for: 1) high plasmid copy number, 2) stability of inheritance, and 3) the majority of beta-lactamase produced in culture. The evolution of gonococcal plasmids may be followed in E. coli, since less defective plasmids produce nonpigmented colonies on congo red agar medium.
将产青霉素酶的淋病奈瑟菌的质粒DNA转移至大肠杆菌后,会产生相对较小的菌落,这些菌落在染料刚果红存在的情况下会变色。向大的、无色素菌落的突变很常见,并且是这些质粒中多种改变的结果。微小质粒的形成是导致无色素菌落的主要改变。然而,三个假定的复制区域中任何一个的缺失都会导致无色素菌落。这些改变后的质粒介导产生的β-内酰胺酶明显少于亲本质粒。在微小质粒内发现并定位了一个新的复制起点。这个起点负责:1)高质粒拷贝数;2)遗传稳定性;3)培养物中产生的大部分β-内酰胺酶。由于缺陷较少的质粒在刚果红琼脂培养基上产生无色素菌落,因此可以在大肠杆菌中追踪淋球菌质粒的进化。