Hayashi K
Gene. 1980 Oct;11(1-2):109-15. doi: 10.1016/0378-1119(80)90091-8.
A new plasmid has been constructed which contains a poly(A) : poly(dT) duplex segment of length approx. 100 base pairs (bp) inserted into the PvuII site of pBR322. This plasmid, pKH47, has all the other restriction sites of pBR322 available for insertion of foreign DNA, and has the same drug resistance genes as does the parental plasmid. The complementary strands of the linearized denatured plasmid DNA can be separated rapidly an efficiently by affinity chromatography with oligo(dA)- and oligo(dT)-cellulose columns in series. More than 90% of the input DNA is recovered as separated strands which can be annealed to form full length double-stranded molecules. One of the applications of the plasmid is to prepare separated complementary strands for sequencing by the chain-terminator technique using DNA primers. This application is illustrated by a sequencing example for a Drosophila DNA insert carrying a tRNA gene.
构建了一种新质粒,它含有一段长度约为100个碱基对(bp)的聚腺苷酸:聚脱氧胸苷酸双链片段,插入到pBR322的PvuII位点。该质粒pKH47具有pBR322的所有其他限制酶切位点,可用于插入外源DNA,并且具有与亲本质粒相同的耐药基因。线性化的变性质粒DNA的互补链可以通过串联的寡聚脱氧腺苷酸和寡聚脱氧胸苷酸纤维素柱进行亲和层析,快速有效地分离。超过90%的输入DNA以分离的单链形式回收,这些单链可以退火形成全长双链分子。该质粒的应用之一是通过使用DNA引物的链终止技术制备用于测序的分离互补链。通过对携带tRNA基因的果蝇DNA插入片段进行测序的例子来说明这种应用。