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Structural investigation of the antagonist LPS from the cyanobacterium Oscillatoria planktothrix FP1

机译:蓝藻颤藻FP1拮抗LPS的结构研究

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Cyanobacteria are aquatic and photosynthetic microorganisms, which contribute up to 30% of the yearly oxygen production on the earth. They have the distinction of being the oldest known fossils, more than 3.5 billion years old, and are one of the largest and most important groups of bacteria on earth. Cyanobacteria are an emerging source of potentially pharmacologically active products and, among these, there are the lipopolysaccharides. Despite their significant and well documented activity, very little is known about the cyanobacteria lipopolysaccharides (LPS) structure. The aim of this work is to investigate the structure of the highly TLR4-antagonist lipopolysaccharide from the cyanobacterium Oscillatoria plankthotrix FP1. The LPS was purified and analysed by means of chemical analysis and ~1H and ~(13)C NMR spectroscopy. The LPS was then degraded by Smith degradation, HF and acetic acid hydrolyses. All the obtained products were investigated in detail by chemical analysis, NMR spectroscopy and by mass spectrometry. The LPS consists of a high molecular mass and very complex molecule lacking Kdo and heptose residues, where the polysaccharide chain is mainly constituted by a backbone of 3-substituted a-L-rhamnose units. The core region is rich in galacturonic acid and mannose residues. Moreover a glycolipid portion, similar to Gram-negative lipid A, was identified. This was built up of a non phosphorylated (10?6) linked glucosamine disaccharide, acylated with 3-hydroxylated fatty acids. In particular 3-hydroxypentadecanoic and 3-hydroxyesadecanoic acids were found, together with esadecanoic and tetradecanoic ones. Finally the presence of a galacturonic acid residue at 6-position of the distal glucosamine in place of the Kdo residue is suggested.
机译:蓝细菌是水生和光合微生物,它们占地球每年氧气产量的30%。它们的区别是已知的最古老的化石,已有超过35亿年的历史,并且是地球上最大,最重要的细菌群之一。蓝细菌是潜在药理活性产品的新兴来源,其中包括脂多糖。尽管它们的活性显着并有据可查,但对蓝细菌脂多糖(LPS)结构的了解却很少。这项工作的目的是研究来自蓝藻颤藻FP1的高度TLR4拮抗剂脂多糖的结构。通过化学分析,〜1H和〜(13)C NMR光谱对LPS进行纯化和分析。然后通过Smith降解,HF和乙酸水解来降解LPS。通过化学分析,NMR光谱和质谱对所有获得的产物进行了详细研究。 LPS由缺乏Kdo和庚糖残基的高分子量和非常复杂的分子组成,其中多糖链主要由3-取代的α-L-鼠李糖单元的主链构成。核心区域富含半乳糖醛酸和甘露糖残基。此外,鉴定出类似于革兰氏阴性脂质A的糖脂部分。这是由一个非磷酸化的(10→6)连接的葡糖胺二糖构成的,该糖被3-羟基化的脂肪酸酰化。特别是发现了3-羟基十五烷酸和3-羟基十八烷酸,以及十八烷酸和十四烷酸。最后,建议在远端葡糖胺的6-位存在半乳糖醛酸残基代替Kdo残基。

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