Umeno M, Sasaki M, Anai M, Takagi Y
Biochem Biophys Res Commun. 1983 Nov 15;116(3):1144-50. doi: 10.1016/s0006-291x(83)80262-9.
The properties of the recB and recC gene products of Escherichia coli were studied using recB and recC gene-inserted plasmids. recB mutants and recC mutants lacked ATP-dependent DNase (recBC enzyme) but showed apparent recovery of enzyme activity on introduction of plasmids carrying the recB and recC gene, respectively. The ATP-dependent DNase was also constructed in vitro by mixing the recB and recC gene products encoded by the plasmids with the corresponding gene. Specific labeling of plasmid-encoded proteins by the maxicell method showed that the recB and recC gene products were 135,000 and 125,000 dalton proteins, respectively. These results suggest that the recB and recC genes are the structural genes of the beta and alpha subunits, respectively, of the recBC enzyme. A gene that encodes a protein of about 100,000 daltons was found to be located between the recB and recC genes. But the product of this gene was shown not to be included in the recBC enzyme.
利用携带recB和recC基因的插入质粒研究了大肠杆菌recB和recC基因产物的特性。recB突变体和recC突变体缺乏ATP依赖性脱氧核糖核酸酶(recBC酶),但分别在导入携带recB和recC基因的质粒后,酶活性出现明显恢复。通过将质粒编码的recB和recC基因产物与相应基因混合,还在体外构建了ATP依赖性脱氧核糖核酸酶。用大细胞法对质粒编码蛋白进行特异性标记表明,recB和recC基因产物分别是135,000道尔顿和125,000道尔顿的蛋白质。这些结果表明,recB和recC基因分别是recBC酶的β亚基和α亚基的结构基因。发现一个编码约100,000道尔顿蛋白质的基因位于recB和recC基因之间。但该基因的产物未包含在recBC酶中。