Saparbaev M K, Mazin A V, Ovchinnikova L P, Dianov G L, Salganik R I
Mol Gen Mikrobiol Virusol. 1988 Feb(2):12-6.
A new method for obtaining the recombinant DNA based on heteroduplex-initiated site-directed insertion of alien nucleotide sequences is proposed. To generate a single-stranded region, plasmid DNA was nicked with restriction endonuclease in the presence of ethidium bromide with subsequent exonuclease III controlled digestion. The inserted DNA sequences flanked by nucleotide sequences complementary to single-stranded region were annealed with plasmid DNA and E. coli cells were transformed by the resulting heteroduplex molecules. The presented data show the possibility to insert as many as 200 nucleotides. The yield of recombinant DNA varied from 16 to 0.7% as the number of nucleotides inserted correspondingly varied from 15 to 200. The site of insertion does not depend crucially on the localization of the restriction site used.
提出了一种基于异源双链引发的外源核苷酸序列定点插入来获得重组DNA的新方法。为了产生单链区域,在溴化乙锭存在的情况下用限制性内切酶切割质粒DNA,随后进行核酸外切酶III控制的消化。将两侧带有与单链区域互补的核苷酸序列的插入DNA序列与质粒DNA退火,并通过所得的异源双链分子转化大肠杆菌细胞。给出的数据表明插入多达200个核苷酸是可能的。随着插入的核苷酸数量相应地从15个变化到200个,重组DNA的产量从16%变化到0.7%。插入位点并不关键地取决于所使用的限制位点的定位。