Nesvera J, Pátek M, Hochmannová J, Abrhámová Z, Becvárová V, Jelínkova M, Vohradský J
Institute of Microbiology, Academy of Sciences of the Czech Republic, Prague.
J Bacteriol. 1997 Mar;179(5):1525-32. doi: 10.1128/jb.179.5.1525-1532.1997.
The complete nucleotide sequence (4,826 bp) of the cryptic plasmid pGA1 from Corynebacterium glutamicum was determined. DNA sequence analysis revealed four putative coding regions (open reading frame A [ORFA], ORFA2, ORFB, and ORFC). ORFC was identified as a rep gene coding for an initiator of plasmid replication (Rep) according to the high level of homology of its deduced amino acid sequence with the Rep proteins of plasmids pSR1 (from C. glutamicum) and pNG2 (from Corynebacterium diphtheriae). This function was confirmed by deletion mapping of the minimal replicon of pGA1 (1.7 kb) which contains only ORFC. Deletion derivatives of pGA1 devoid of ORFA exhibited significant decreases in the copy number in C. glutamicum cells and displayed segregational instability. Introduction of ORFA in trans into the cells harboring these deletion plasmids dramatically increased their copy number and segregational stability. The ORFA gene product thus positively influences plasmid copy number. This is the first report on such activity associated with a nonintegrating bacterial plasmid. The related plasmids pGA1, pSR1, and pNG2 lacking significant homology with any other plasmid seem to be representatives of a new group of plasmids replicating in the rolling-circle mode.
测定了谷氨酸棒杆菌隐蔽质粒pGA1的完整核苷酸序列(4826 bp)。DNA序列分析揭示了四个推定的编码区(开放阅读框A [ORFA]、ORFA2、ORFB和ORFC)。根据其推导的氨基酸序列与质粒pSR1(来自谷氨酸棒杆菌)和pNG2(来自白喉棒杆菌)的Rep蛋白的高度同源性,ORFC被鉴定为一个编码质粒复制起始蛋白(Rep)的rep基因。通过对仅包含ORFC的pGA1最小复制子(1.7 kb)进行缺失图谱分析,证实了该功能。缺失ORFA的pGA1缺失衍生物在谷氨酸棒杆菌细胞中的拷贝数显著降低,并表现出分离不稳定性。将ORFA反式导入携带这些缺失质粒的细胞中,显著增加了它们的拷贝数和分离稳定性。因此,ORFA基因产物对质粒拷贝数有正向影响。这是关于与非整合型细菌质粒相关的此类活性的首次报道。与任何其他质粒缺乏显著同源性的相关质粒pGA1、pSR1和pNG2似乎是在滚环模式下复制的一组新质粒的代表。