Abe Akiko, Koide Hidekatsu, Kohno Takeyuki, Watabe Kazuhito
Faculty of Pharmaceutical Sciences, Setsunan University, 45-1, Nagaotoge-cho, Hirakata, Osaka 573-01, Japan.
Meditopia Research Center, 43-6, Hongo 3-chome, Bunkyo-ku, Tokyo 113, Japan.
Microbiology (Reading). 1995 Jun;141 ( Pt 6):1433-1442. doi: 10.1099/13500872-141-6-1433.
A gene, cotS, encoding a spore coat polypeptide of Bacillus subtilis, was isolated from an EcoRI fragment (5.4 kb) of the chromosome by using synthetic oligonucleotide probes corresponding to the NH2-terminal amino acid sequence of Cot40-2 previously purified from the spore coat of B. subtilis. The nucleotide sequence (2603 bp) was determined and sequence analysis suggested the presence of two contiguous ORFs, ORF X and cotS, followed by the 5'-region of an additional ORF, ORF Y, downstream of cotS. The cotS gene is 1053 nucleotides long and encodes a polypeptide of 351 amino acids with a predicted molecular mass of 41083 Da. The predicted amino acid sequence was in complete agreement with the NH2-terminal amino acid sequence of Cot40-2. The orfX gene is 1131 nucleotides long and encodes a polypeptide of 377 amino acids with a predicted molecular mass of 42911 Da. The gene product of cotS was confirmed to be identical to Cot40-2 by SDS-PAGE and immunoblotting from Escherichia coli transformed with a plasmid containing the cotS region. Northern hybridization analysis indicated that a transcript of cotS and orfX appeared at about 5 h after the onset of sporulation. The transcriptional start point determined by primer extension analysis suggested that -10 and -35 regions are present upstream of orfX and are very similar to the consensus sequence for the sigma k-dependent promoter. Terminator-like sequences were not found in the DNA fragment (2603 bp) sequenced in this paper, which suggested that the cotS locus may be part of a multicistronic operon. The cotS gene is located between dnaB and degQ at about 270-275 degrees on the genetic map. Insertional mutagenesis of the cotS gene by introducing an integrative plasmid resulted in no alteration of growth or sporulation, and had no effect on germination or resistance to chloroform.
通过使用与先前从枯草芽孢杆菌芽孢衣中纯化的Cot40 - 2的NH2末端氨基酸序列相对应的合成寡核苷酸探针,从染色体的EcoRI片段(5.4 kb)中分离出了一个编码枯草芽孢杆菌芽孢衣多肽的基因cotS。测定了核苷酸序列(2603 bp),序列分析表明存在两个相邻的开放阅读框,即ORF X和cotS,在cotS下游紧接着另一个开放阅读框ORF Y的5'区域。cotS基因长1053个核苷酸,编码一个由351个氨基酸组成的多肽,预测分子量为41083 Da。预测的氨基酸序列与Cot40 - 2的NH2末端氨基酸序列完全一致。orfX基因长1131个核苷酸,编码一个由377个氨基酸组成的多肽,预测分子量为42911 Da。通过SDS - PAGE和免疫印迹法,从用含有cotS区域的质粒转化的大肠杆菌中证实了cotS的基因产物与Cot40 - 2相同。Northern杂交分析表明,cotS和orfX的转录本在芽孢形成开始后约5小时出现。通过引物延伸分析确定的转录起始点表明,- 10和- 35区域存在于orfX上游,并且与依赖于σk的启动子的共有序列非常相似。在本文测序的DNA片段(2603 bp)中未发现类似终止子的序列,这表明cotS基因座可能是一个多顺反子操纵子的一部分。cotS基因在遗传图谱上位于dnaB和degQ之间,大约在270 - 275度处。通过引入整合质粒对cotS基因进行插入诱变,未导致生长或芽孢形成的改变,对萌发或对氯仿的抗性也没有影响。