Pedersen L B, Angert E R, Setlow P
Department of Biochemistry, University of Connecticut Health Center, Farmington, Connecticut 06032, USA.
J Bacteriol. 1999 May;181(10):3201-11. doi: 10.1128/JB.181.10.3201-3211.1999.
Previous studies have shown that Bacillus subtilis cells lacking penicillin-binding protein 1 (PBP1), encoded by ponA, have a reduced growth rate in a variety of growth media and are longer, thinner, and more bent than wild-type cells. It was also recently shown that cells lacking PBP1 require increased levels of divalent cations for growth and are either unable to grow or grow as filaments in media low in Mg2+, suggesting a possible involvement of PBP1 in septum formation under these conditions. Using epitope-tagging and immunofluorescence microscopy, we have now shown that PBP1 is localized at division sites in vegetative cells of B. subtilis. In addition, we have used fluorescence and electron microscopy to show that growing ponA mutant cells display a significant septation defect, and finally by immunofluorescence microscopy we have found that while FtsZ localizes normally in most ponA mutant cells, a significant proportion of ponA mutant cells display FtsZ rings with aberrant structure or improper localization, suggesting that lack of PBP1 affects FtsZ ring stability or assembly. These results provide strong evidence that PBP1 is localized to and has an important function in the division septum in B. subtilis. This is the first example of a high-molecular-weight class A PBP that is localized to the bacterial division septum.
先前的研究表明,缺乏由ponA编码的青霉素结合蛋白1(PBP1)的枯草芽孢杆菌细胞,在多种生长培养基中的生长速率降低,并且比野生型细胞更长、更细且更弯曲。最近还表明,缺乏PBP1的细胞生长需要更高水平的二价阳离子,并且在Mg2+含量低的培养基中要么无法生长,要么以丝状生长,这表明在这些条件下PBP1可能参与隔膜形成。通过表位标记和免疫荧光显微镜技术,我们现在已经表明PBP1定位于枯草芽孢杆菌营养细胞的分裂位点。此外,我们使用荧光和电子显微镜表明,生长中的ponA突变体细胞表现出明显的隔膜缺陷,最后通过免疫荧光显微镜我们发现,虽然FtsZ在大多数ponA突变体细胞中正常定位,但相当一部分ponA突变体细胞显示出结构异常或定位不当的FtsZ环,这表明缺乏PBP1会影响FtsZ环的稳定性或组装。这些结果提供了强有力的证据,证明PBP1定位于枯草芽孢杆菌的分裂隔膜并在其中发挥重要功能。这是高分子量A类PBP定位于细菌分裂隔膜的首个例子。