Murray T, Popham D L, Setlow P
Department of Biochemistry, University of Connecticut Health Center, Farmington 06030, USA.
J Bacteriol. 1996 Oct;178(20):6001-5. doi: 10.1128/jb.178.20.6001-6005.1996.
Penicillin-binding proteins (PBPs) are enzymes involved in the synthesis of peptidoglycan structures in Bacillus subtilis such as the vegetative cell wall and the spore cortex. The B. subtilis sequencing project has identified a gene (orf16, EMBL accession number D38161) which exhibits significant sequence similarity to genes encoding class B high-molecular-weight PBPs. We have found that orf16 encodes PBP3 and have renamed this locus pbpC. Transcriptional fusions to lacZ were used to demonstrate that pbpC is transcribed primarily during log-phase growth, with lower amounts expressed during sporulation. During spore germination and outgrowth, pbpC expression resumes coincident with an increase in the optical density of the culture. The major promoter for pbpC is located just upstream of the gene; a low level of expression during sporulation appears to originate from much further upstream. Loss of PBP3 does not produce any detectable change in phenotype with respect to cell morphology, growth, sporulation, spore heat resistance, or spore germination and outgrowth. This was also true when the pbpC mutation was combined with mutations affecting other PBP-encoding genes to produce double mutants. These findings are consistent with previous evidence that many PBPs of B. subtilis have redundant functions within the cell.
青霉素结合蛋白(PBPs)是参与枯草芽孢杆菌肽聚糖结构合成的酶,如营养细胞壁和芽孢皮层。枯草芽孢杆菌测序项目鉴定出一个基因(orf16,EMBL登录号D38161),它与编码B类高分子量PBPs的基因具有显著的序列相似性。我们发现orf16编码PBP3,并将该基因座重新命名为pbpC。利用与lacZ的转录融合来证明pbpC主要在对数生长期转录,在芽孢形成过程中表达量较低。在芽孢萌发和生长过程中,pbpC的表达恢复,与培养物光密度的增加同时发生。pbpC的主要启动子位于该基因的上游;芽孢形成过程中的低水平表达似乎起源于更上游。PBP3的缺失在细胞形态、生长、芽孢形成、芽孢耐热性或芽孢萌发及生长方面未产生任何可检测到的表型变化。当pbpC突变与影响其他PBP编码基因的突变组合产生双突变体时,情况也是如此。这些发现与之前枯草芽孢杆菌许多PBPs在细胞内具有冗余功能的证据一致。