Moore R J, Krishnapillai V
J Bacteriol. 1982 Jan;149(1):284-93. doi: 10.1128/jb.149.1.284-293.1982.
We isolated deletion mutants of Pseudomonas aeruginosa plasmid R91-5 by both in vitro and in vivo means. Many of the deletion mutants selected on the basis of resistance to donor-specific phages fell into a few groups of apparently identical mutants, although the mutants were nonsibs. By analyzing plasmids with large deletions, we found that the essential replication genes of R91-5 were within a 3.85-kilobase region between coordinates 45.5 and 48.9. The origin of plasmid transfer (oriT) was mapped to a 4.5-kilobase region between coordinates 1.7 and 6.2. We indirectly determined the direction of plasmid transfer from oriT. By combining the data from our analysis of the deletions with data from complementation tests between cloned R91-5 fragments and known reference mutants, we ordered and mapped the 10 known transfer (tra) cistrons of R91-5. All of the tra cistrons mapped within the Tra2 region, and their order was as follows: traX, -Y, -T, -Q, -(V, R), -U, -(S, Z), -W (the cistrons in parentheses could not be ordered with respect to each other).
我们通过体外和体内方法分离出了铜绿假单胞菌质粒R91 - 5的缺失突变体。许多基于对供体特异性噬菌体的抗性而选择的缺失突变体虽不是同胞突变体,但却分成了几组明显相同的突变体。通过分析具有大段缺失的质粒,我们发现R91 - 5的必需复制基因位于坐标45.5和48.9之间的一个3.85千碱基区域内。质粒转移起始点(oriT)被定位到坐标1.7和6.2之间的一个4.5千碱基区域。我们间接确定了从oriT开始的质粒转移方向。通过将缺失分析数据与克隆的R91 - 5片段和已知参考突变体之间的互补试验数据相结合,我们对R91 - 5的10个已知转移(tra)顺反子进行了排序和定位。所有tra顺反子都定位在Tra2区域内,其顺序如下:traX、-Y、-T、-Q、-(V, R)、-U、-(S, Z)、-W(括号中的顺反子彼此之间无法排序)。