From the Infection Biology Department, Interfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, 72076 Tübingen, Germany,
the German Center for Infection Research, Partner Site Tübingen, University of Tübingen, 72076 Tübingen, Germany, and.
J Biol Chem. 2018 Sep 21;293(38):14916-14924. doi: 10.1074/jbc.RA118.004584. Epub 2018 Aug 1.
is part of the human nasal and skin microbiomes along with other bacterial commensals and opportunistic pathogens. Nutrients are scarce in these habitats, demanding effective nutrient acquisition and competition strategies. How copes with phosphate limitation is still unknown. Wall teichoic acid (WTA), a polyol-phosphate polymer, could serve as a phosphate source, but whether can utilize it during phosphate starvation remains unknown. secretes a glycerophosphodiesterase, GlpQ, that cleaves a broad variety of glycerol-3-phosphate (GroP) headgroups of deacylated phospholipids, providing this bacterium with GroP as a carbon and phosphate source. Here we demonstrate that GlpQ can also use glycerophosphoglycerol derived from GroP WTA from coagulase-negative , , and , which share the nasal and skin habitats with Therefore, GlpQ is the first reported WTA-hydrolyzing enzyme, or teichoicase, from Activity assays revealed that unmodified WTA is the preferred GlpQ substrate, and the results from MS analysis suggested that GlpQ uses an exolytic cleavage mechanism. Importantly, GlpQ did not hydrolyze the ribitol-5-phosphate WTA polymers of , underscoring its role in interspecies competition rather than in cell wall homeostasis or WTA recycling. expression was strongly up-regulated under phosphate limitation, and GlpQ allowed to grow in the presence of GroP WTA as the sole phosphate source. Our study reveals a novel and unprecedented strategy of for acquiring phosphate from bacterial competitors under the phosphate-limiting conditions in the nasal or skin environments.
是人类鼻腔和皮肤微生物组的一部分,与其他细菌共生体和机会性病原体共存。这些栖息地的营养物质稀缺,需要有效的营养获取和竞争策略。目前尚不清楚 如何应对磷酸盐限制。细胞壁磷壁酸 (WTA) 是一种多元醇-磷酸盐聚合物,可用作磷酸盐源,但 是否能在磷酸盐饥饿期间利用它仍然未知。 分泌一种甘油磷酸二酯酶,GlpQ,它可以裂解各种去酰化磷脂的甘油-3-磷酸 (GroP) 头基,为该细菌提供 GroP 作为碳和磷酸盐源。在这里,我们证明 GlpQ 还可以利用来自凝固酶阴性 的 GroP WTA 衍生的甘油磷酸甘油, 和 与 共享鼻腔和皮肤栖息地。因此, GlpQ 是第一个被报道的 WTA 水解酶,或磷壁酸酶,来自 。活性测定表明,未修饰的 WTA 是 GlpQ 的首选底物,MS 分析结果表明 GlpQ 使用外切酶裂解机制。重要的是,GlpQ 不能水解 的核糖醇-5-磷酸 WTA 聚合物,这突出了它在种间竞争中的作用,而不是在 细胞壁内稳态或 WTA 回收中。 在磷酸盐限制下的表达被强烈上调,并且 GlpQ 允许 在 GroP WTA 作为唯一的磷酸盐源存在的情况下生长。我们的研究揭示了 在鼻腔或皮肤环境中磷酸盐限制条件下从细菌竞争中获取磷酸盐的一种新颖且前所未有的策略。