Abo T, Inamoto S, Ohtsubo E
Institute of Applied Microbiology, University of Tokyo, Japan.
J Bacteriol. 1991 Oct;173(20):6347-54. doi: 10.1128/jb.173.20.6347-6354.1991.
The product of the traM gene of plasmid R100 was purified as the TraM-collagen-beta-galactosidase fusion protein (TraM*) by using a beta-galactosidase-specific affinity column, and the TraM portion of TraM* (TraM') was separated by collagenolysis. Both the TraM* and TraM' proteins were found to bind specifically to a broad region preceding the traM gene. This region (designated sbm) was located within the nonconserved region in oriT among conjugative plasmids related to R100. The region seems to contain four core binding sites (designated sbmA, sbmB, sbmC, and sbmD), each consisting of a similar number of nucleotides and including a homologous 15-bp sequence. This result, together with the observation that the TraM* protein was located in the membrane fraction, indicates the possibility that the TraM protein has a function in anchoring the oriT region of R100 at the sbm sites to the membrane pore, through which the single-stranded DNA is transferred to the recipient. sbmC and sbmD, each of which contained a characteristic inverted repeat sequence, overlapped with the promoter region for the traM gene. This suggests that the expression of the traM gene may be regulated by its own product.
通过使用β-半乳糖苷酶特异性亲和柱,将质粒R100的traM基因产物纯化为TraM-胶原蛋白-β-半乳糖苷酶融合蛋白(TraM*),并通过胶原酶解分离TraM的TraM部分(TraM')。发现TraM和TraM'蛋白都能特异性结合traM基因之前的一个广泛区域。该区域(命名为sbm)位于与R100相关的接合质粒oriT中的非保守区域内。该区域似乎包含四个核心结合位点(命名为sbmA、sbmB、sbmC和sbmD),每个位点由相似数量的核苷酸组成,并包含一个同源的15个碱基对的序列。这一结果,连同观察到TraM*蛋白位于膜组分中,表明TraM蛋白可能具有将R100的oriT区域在sbm位点锚定到膜孔的功能,单链DNA通过该膜孔转移到受体中。sbmC和sbmD各自包含一个特征性的反向重复序列,与traM基因的启动子区域重叠。这表明traM基因的表达可能受其自身产物的调控。