Watabe K, Forough R
Biochem Biophys Res Commun. 1987 Jun 15;145(2):861-7. doi: 10.1016/0006-291x(87)91044-8.
In order to detect the product of dnaB gene in B. subtilis, a gene which is involved in the initiation of DNA replication and the formation of the DNA-membrane complex, we synthesized an origopeptide of 15 amino acids which corresponds to a region near the carboxyl-terminal of the gene product, and raised antibody against the synthetic peptide. We have also employed a filter binding assay to measure the predicted DNA binding activity of the product of the dnaB gene, using the plasmid pUB110. The binding activity was detected after fractionation of cell lysates of B. subtilis on sucrose-density gradients. When the active fraction was prepared from a mutant which was temperature-sensitive for the dnaB gene, the DNA binding activity in the fraction showed significant thermolability. Furthermore, the binding activity was inhibited by the purified antibody raised against the synthetic peptide. These results suggest that the product of the dnaB gene does indeed have DNA binding activity, and that the filter binding assay and the antibody can be used for the detection and characterization of the gene product.
为了检测枯草芽孢杆菌中参与DNA复制起始和DNA-膜复合物形成的dnaB基因的产物,我们合成了一段由15个氨基酸组成的原肽,该原肽对应于基因产物羧基末端附近的一个区域,并制备了针对该合成肽的抗体。我们还采用了滤膜结合试验,使用质粒pUB110来测量dnaB基因产物预测的DNA结合活性。在枯草芽孢杆菌细胞裂解物在蔗糖密度梯度上分级分离后检测到了结合活性。当从对dnaB基因温度敏感的突变体中制备活性组分时,该组分中的DNA结合活性表现出明显的热稳定性。此外,针对合成肽制备的纯化抗体抑制了结合活性。这些结果表明,dnaB基因的产物确实具有DNA结合活性,并且滤膜结合试验和抗体可用于该基因产物的检测和特性鉴定。