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Regions of broad-host-range plasmid RK2 which are essential for replication and maintenance.

机译:宿主范围广的质粒RK2的区域对复制和维持至关重要。

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摘要

The sites of cleavage on the map of the broad-host-range plasmid RK2 (56 kilobases) were determined for the BglII, PstI, and SmaI restriction enzymes, and the determinants for tetracycline and ampicillin resistance were localized. The cleavage sites were clustered at or near the drug resistance genes. To localize regions required for plasmid replication and maintenance in Escherichia coli, we deleted nonessential regions of RK2 by partial digestion with the restriction endonuclease HaeII to produce small derivatives. The smallest stable replicon obtained contained five HaeII fragments of RK2 which total 5.4 kilobases. These fragments were derived from three regions of RK2 that are separated from each other by antibiotic resistance genes. One of these HaeII fragments (0.75 kilobases) has the properties expected of the origin of replication. The outer four fragments, located in two separate regions of RK2, were found to provide, in trans, functions that permit the replication of the HaeII fragment carrying the origin of the replication. These results indicate that at least two plasmid-encoded genes, capable of acting in trans, and a replication origin are required for RK2 replication and maintenance.
机译:确定了在宽宿主范围的质粒RK2(56千碱基)的图谱上的切割位点,用于BglII,PstI和SmaI限制酶,并确定了四环素和氨苄青霉素抗性的决定因素。切割位点聚集在耐药基因处或附近。为了在大肠杆菌中定位质粒复制和维持所需的区域,我们通过用限制性内切酶HaeII部分消化以产生小衍生物来删除RK2的非必需区域。获得的最小的稳定复制子包含五个RK2的HaeII片段,总计5.4公里。这些片段来自RK2的三个区域,这些区域通过抗生素抗性基因相互分隔。这些HaeII片段之一(0.75千碱基)具有复制起点所期望的特性。发现位于RK2的两个单独区域中的外部四个片段反式提供允许复制带有复制起点的HaeII片段的功能。这些结果表明,至少两个能够反式起作用的质粒编码基因和复制起点是RK2复制和维持所必需的。

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