Włodarczyk M, Bednarska M
Acta Microbiol Pol. 1978;27(4):321-9.
The plasmid R6K has been introduced into a number of Escherichia coli polymerase deficient (pol) mutants. In polCts mutants transferred to the nonpermissive temperature to inactivate polymerase III, R6K replicates but the replication products have a density in dye-CsCl gradients intermediate between supercoiled and linear forms. This aberrant replication requires normal cellular levels of polymerase I since it does not occur in polA polCts mutants. Normal R6K replication and maintenance occur in a polA polB polC+ host, however, we cannot tell from our experiments wheather polymerase I or III replicates R6K in polA+ polC+ host. Polymerase II, the polB gene product, has no detectable role in R6K replication.
质粒R6K已被导入多种大肠杆菌聚合酶缺陷(pol)突变体中。在转移到非允许温度以灭活聚合酶III的polCts突变体中,R6K能够复制,但复制产物在染料-氯化铯梯度中的密度介于超螺旋形式和线性形式之间。这种异常复制需要正常细胞水平的聚合酶I,因为它在polA polCts突变体中不会发生。正常的R6K复制和维持发生在polA polB polC+宿主中,然而,从我们的实验中我们无法判断在polA+ polC+宿主中是聚合酶I还是III复制R6K。聚合酶II,即polB基因产物,在R6K复制中没有可检测到的作用。