Guiard B, Buhler J M
Biochimie. 1984 Feb;66(2):151-8. doi: 10.1016/0300-9084(84)90204-9.
An efficient technique was used to clone the gene for yeast cytochrome b2, (a nuclear encoded mitochondrial protein) using the expression vector, lambda gt11 (lac 5 nin 5 c1857 S100). This enables the insertion of yeast DNA into the beta-galactosidase structural gene (lacZ) and promotes synthesis of hybrid proteins. Screening of antigen producing clones in the lambda gt11 recombinant genomic library was achieved using antiserum against cytochrome b2 according to Young and Davis (1983) Two recombinants containing part of the gene coding for cytochrome b2 were isolated and characterized as follows: by their expression in Escherichia coli cells, examined by immuno-blotting with antibodies to pure cytochrome b2. by DNA sequence analysis. One recombinant carries a 3 Kb yeast DNA insert which contains the whole nucleotide sequence encoding cytochrome b2 and a few amino acids of the amino terminal presequence.
采用一种高效技术,利用表达载体λgt11(lac5 nin5 c1857 S100)克隆酵母细胞色素b2基因(一种核编码的线粒体蛋白)。这使得酵母DNA能够插入β-半乳糖苷酶结构基因(lacZ)并促进杂交蛋白的合成。根据扬和戴维斯(1983年)的方法,使用抗细胞色素b2抗血清对λgt11重组基因组文库中产生抗原的克隆进行筛选。分离出两个含有细胞色素b2编码基因部分片段的重组体,并进行如下鉴定:通过它们在大肠杆菌细胞中的表达,用抗纯细胞色素b2的抗体进行免疫印迹检测;通过DNA序列分析。一个重组体携带一个3kb的酵母DNA插入片段,其中包含编码细胞色素b2的完整核苷酸序列以及氨基末端前序列的几个氨基酸。