Truelsen E, Gausing K, Jochimsen B, Jørgensen P, Marcker K A
Nucleic Acids Res. 1979 Jul 11;6(9):3061-72. doi: 10.1093/nar/6.9.3061.
Double-stranded soybean leghemoglobin DNA was synthesized from leghemoglobin mRNA isolated from soybean nodules. The dsDNA was inserted into the Bam H1 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.
从大豆根瘤中分离出豆血红蛋白mRNA,以此合成了双链大豆豆血红蛋白DNA。采用聚-dAT连接法将双链DNA插入质粒pBR322的Bam H1位点。分离出一个重组质粒的克隆DNA片段,并通过限制性内切酶消化进行表征。插入DNA选定部分的限制性酶切图谱和DNA序列与大豆豆血红蛋白的氨基酸序列完全一致。