Schuster C, Dobrinski B, Hakenbeck R
Max-Planck Institut für Molekulare Genetik, Berlin, Federal Republic of Germany.
J Bacteriol. 1990 Nov;172(11):6499-505. doi: 10.1128/jb.172.11.6499-6505.1990.
An internal 630-bp DNA fragment of the gene encoding penicillin-binding protein 3 (PBP 3) (dacA) of Streptococcus pneumoniae was identified in a lambda gt11 gene bank screened with anti-PBP 3 antiserum. The deduced 210-amino-acid sequence showed a high degree of homology to the low-molecular-weight PBPs 5 and 6 of Escherichia coli and Bacillus subtilis PBP 5. Viable mutants lacking a C-terminal part of PBP 3 were obtained after a plasmid containing the dacA fragment was integrated into the PBP 3 gene by homologous recombination. The truncated PBP 3* was still active in terms of beta-lactam binding. Most PBP 3 was found in the growth medium, indicating that membrane anchoring of PBP 3 is provided by the C terminus, as has been shown for other D,D-carboxypeptidases. The mutant cells grew with a slower generation time than the wild type in the shape of irregular enlarged spheres. In addition, as revealed by electron microscopy, cell separation was severely affected, septa were found unevenly distributed at multiple sites within the cells, and the murein layer appeared variable in thickness.
在用抗青霉素结合蛋白3(PBP 3)抗血清筛选的λgt11基因文库中,鉴定出肺炎链球菌编码青霉素结合蛋白3(PBP 3)(dacA)基因的一段630 bp的内部DNA片段。推导的210个氨基酸序列与大肠杆菌的低分子量PBPs 5和6以及枯草芽孢杆菌PBP 5具有高度同源性。通过同源重组将含有dacA片段的质粒整合到PBP 3基因中后,获得了缺乏PBP 3 C末端部分的活突变体。截短的PBP 3*在β-内酰胺结合方面仍具有活性。大多数PBP 3存在于生长培养基中,这表明PBP 3的膜锚定是由C末端提供的,其他D,D-羧肽酶也是如此。突变细胞的生长代时比野生型慢,呈不规则扩大球体形状。此外,电子显微镜显示,细胞分裂受到严重影响,隔膜在细胞内多个部位分布不均匀,胞壁质层厚度不一。