Sadaie Y, Takamatsu H, Nakamura K, Yamane K
Radioisotope Center, National Institute of Genetics, Mishima, Japan.
Gene. 1991 Feb 1;98(1):101-5. doi: 10.1016/0378-1119(91)90110-w.
We have determined the nucleotide (nt) sequence of the wild-type div+ gene of Bacillus subtilis which complements the temperature-sensitive div-341 mutation and is involved in cell septation, sporulation, secretion of extracellular enzymes, development of competence, autolysis and spore outgrowth. It has an open reading frame encoding 841 amino acids (aa) with homology to the Escherichia coli secA gene, which is involved in protein secretion and cell separation. The deduced aa sequence of the B. subtilis div+ gene shares 50% identity with that of the E. coli secA gene, and highly homologous regions were observed in the N-terminal portions. DNA-DNA hybridization with the E. coli secA gene as the probe showed that the div+ gene could be easily detected by homology and that a single copy of the homologous gene was present in B. subtilis. Since both genes are similar in their functions and deduced aa sequences, we propose that the div+ gene is the counterpart of the secA gene of E. coli.
我们已经确定了枯草芽孢杆菌野生型div+基因的核苷酸(nt)序列,该基因可弥补温度敏感型div-341突变,并参与细胞分裂、孢子形成、细胞外酶的分泌、感受态的发育、自溶和孢子萌发。它有一个开放阅读框,编码841个氨基酸(aa),与大肠杆菌secA基因具有同源性,后者参与蛋白质分泌和细胞分离。枯草芽孢杆菌div+基因推导的氨基酸序列与大肠杆菌secA基因的氨基酸序列有50%的同一性,并且在N端部分观察到高度同源区域。以大肠杆菌secA基因为探针进行DNA-DNA杂交表明,通过同源性很容易检测到div+基因,并且在枯草芽孢杆菌中存在单拷贝的同源基因。由于这两个基因在功能和推导的氨基酸序列上相似,我们认为div+基因是大肠杆菌secA基因的对应物。