Choi K Y, Benisek W F
Department of Biological Chemistry, School of Medicine, University of California, Davis 95616.
Gene. 1987;58(2-3):257-64. doi: 10.1016/0378-1119(87)90380-5.
We have cloned an approx. 5-kb fragment of Pseudomonas testosteroni DNA containing the structural gene of delta 5-3-ketosteroid isomerase into the EcoRI site of the lambda gt11 genome. Escherichia coli infected with these recombinant phages produce a polypeptide which is recognized by antiserum raised against the purified isomerase. Four of the recombinant lambda gt11 clones contain significant levels of isomerase activity and produce an immunopositive polypeptide of the same apparent Mr as the native isomerase obtained from P. testosteroni. The approx. 5-kb fragment hybridizes to synthetic 21-mer and 17-mer oligodeoxynucleotide mixtures corresponding to the 5' and 3' regions, respectively, of the expected nucleotide sequence of the gene.
我们已将含有δ5 - 3 - 酮类固醇异构酶结构基因的约5kb睾丸酮假单胞菌DNA片段克隆到λgt11基因组的EcoRI位点。用这些重组噬菌体感染的大肠杆菌产生一种多肽,该多肽可被针对纯化异构酶产生的抗血清识别。四个重组λgt11克隆含有显著水平的异构酶活性,并产生一种免疫阳性多肽,其表观分子量与从睾丸酮假单胞菌获得的天然异构酶相同。这个约5kb的片段分别与对应于该基因预期核苷酸序列5'和3'区域的合成21聚体和17聚体寡脱氧核苷酸混合物杂交。