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Cloning of soybean leghemoglobin structural gene sequences synthesized in vitro

机译:体外合成大豆豆血红蛋白结构基因序列的克隆

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Double-stranded soybean leghemoglobin DNA was synthesized from leghemoglobin mRNA isolated from soybean nodules. The dsDNA was inserted into the Bam Hl site of plasmid pBR322 using the poly-dAT-joiner method. A cloned DNA fragment of one recombinant plasmid was isolated and characterized by restriction endonuclease digestion. The restriction cleavage map and the DNA sequence of a selected part of the inserted DNA are in complete accordance with the amino-acid sequence of soybean leghemoglobin.
机译:从大豆结节中分离的豆血红蛋白mRNA合成了双链大豆豆血红蛋白DNA。使用poly-dAT-接头方法将dsDNA插入质粒pBR322的Bam H1位点。分离了一个重组质粒的克隆DNA片段,并通过限制性核酸内切酶消化进行了表征。限制性切割图和插入的DNA的选定部分的DNA序列与大豆豆血红蛋白的氨基酸序列完全一致。

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