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A Second Galacturonic Acid Transferase Is Required for Core Lipopolysaccharide Biosynthesis and Complete Capsule Association with the Cell Surface in Klebsiella pneumoniae

机译:核心脂多糖生物合成和与肺炎克雷伯菌的细胞表面完全胶囊缔合需要第二个半乳糖醛酸转移酶

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The core lipopolysaccharide (LPS) of Klebsiella pneumoniae contains two galacturonic acid (GalA) residues, but only one GalA transferase (WabG) has been identified. Data from chemical and structural analysis of LPS isolated from a wabO mutant show the absence of the inner core β-GalA residue linked to l-glycero-d-manno-heptose III (l,d-Hep III). An in vitro assay demonstrates that the purified WabO is able to catalyze the transfer of GalA from UDP-GalA to the acceptor LPS isolated from the wabO mutant, but not to LPS isolated from waaQ mutant (deficient in l,d-Hep III). The absence of this inner core β-GalA residue results in a decrease in virulence in a capsule-dependent experimental mouse pneumonia model. In addition, this mutation leads to a strong reduction in cell-bound capsule. Interestingly, a K66 Klebsiella strain (natural isolate) without a functional wabO gene shows reduced levels of cell-bound capsule in comparison to those of other K66 strains. Thus, the WabO enzyme plays an important role in core LPS biosynthesis and determines the level of cell-bound capsule in Klebsiella pneumoniae.
机译:肺炎克雷伯菌的核心脂多糖(LPS)包含两个半乳糖醛酸(GalA)残基,但仅鉴定出一个GalA转移酶(WabG)。从 wabO 突变体分离的LPS的化学和结构分析数据表明,不存在与l- 甘油 -d- 甘露糖有关的内在β-GalA残基-庚糖III(l,d-Hep III)。体外试验表明,纯化的WabO能够催化GalA从UDP-GalA转移到从 wabO 突变体分离的受体LPS,但不能转移到从 waaQ 分离的LPS。 em>突变体(缺乏1,d-Hep III)。在胶囊依赖性实验性小鼠肺炎模型中,缺少这种内在的β-GalA内在残基会导致毒力降低。另外,这种突变导致细胞结合的胶囊强烈减少。有趣的是,与其他K66菌株相比,没有功能性 wabO 基因的K66 克雷伯菌菌株(天然分离株)显示出降低的细胞结合胶囊水平。因此,WabO酶在核心脂多糖的生物合成中起着重要作用,并决定了肺炎克雷伯菌的细胞结合胶囊的水平。

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