Fukushima Tatsuya, Yamamoto Hiroki, Atrih Abdelmadjid, Foster Simon J, Sekiguchi Junichi
Department of Applied Biology, Faculty of Textile Science and Technology, Shinshu University, Ueda-shi, Nagano 386, Japan.
J Bacteriol. 2002 Nov;184(21):6007-15. doi: 10.1128/JB.184.21.6007-6015.2002.
The predicted amino acid sequence of Bacillus subtilis yfjS (renamed pdaA) exhibits high similarity to those of several polysaccharide deacetylases. Beta-galactosidase fusion experiments and results of Northern hybridization with sporulation sigma mutants indicated that the pdaA gene is transcribed by E(sigma)(G) RNA polymerase. pdaA-deficient spores were bright by phase-contrast microscopy, and the spores were induced to germination on the addition of L-alanine. Germination-associated spore darkening, a slow and partial decrease in absorbance, and slightly lower dipicolinic acid release compared with that by the wild-type strain were observed. In particular, the release of hexosamine-containing materials was lacking in the pdaA mutant. Muropeptide analysis indicated that the pdaA-deficient spores completely lacked muramic delta-lactam. A pdaA-gfp fusion protein constructed in strain 168 and pdaA-deficient strains indicated that the protein is localized in B. subtilis spores. The biosynthetic pathway of muramic delta-lactam is discussed.
枯草芽孢杆菌yfjS(重新命名为pdaA)的预测氨基酸序列与几种多糖脱乙酰酶的序列高度相似。β-半乳糖苷酶融合实验以及与芽孢形成σ突变体的Northern杂交结果表明,pdaA基因由E(σ)(G) RNA聚合酶转录。通过相差显微镜观察,pdaA缺陷型芽孢颜色较亮,添加L-丙氨酸后芽孢被诱导萌发。与野生型菌株相比,观察到萌发相关的芽孢变暗、吸光度缓慢且部分降低以及吡啶二羧酸释放量略低。特别是,pdaA突变体中缺乏含己糖胺物质的释放。胞壁肽分析表明,pdaA缺陷型芽孢完全缺乏胞壁酸δ-内酰胺。在168菌株和pdaA缺陷型菌株中构建的pdaA-gfp融合蛋白表明该蛋白定位于枯草芽孢杆菌芽孢中。文中讨论了胞壁酸δ-内酰胺的生物合成途径。