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首页> 外文期刊>Proteome science >In silico biosynthesis of virenose, a methylated deoxy-sugar unique to Coxiella burnetii lipopolysaccharide
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In silico biosynthesis of virenose, a methylated deoxy-sugar unique to Coxiella burnetii lipopolysaccharide

机译:硅酮的计算机化生物合成,这是伯氏柯氏杆菌脂多糖特有的甲基化脱氧糖

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Background Coxiella burnetii is Gram-negative bacterium responsible for the zoonosis Q-fever. While it has an obligate intracellular growth habit, it is able to persist for extended periods outside of a host cell and can resist environmental conditions that would be lethal to most prokaryotes. It is these extracellular bacteria that are the infectious stage encountered by eukaryotic hosts. The intracellular form has evolved to grow and replicate within acidified parasitophorous vacuoles. The outer coat of C. burnetii comprises a complex lipopolysaccharide (LPS) component that includes the unique methylated-6-deoxyhexose, virenose. Although potentially important as a biomarker for C. burnetii, the pathway for its biosynthesis remains obscure. Results The 6-deoxyhexoses constitute a large family integral to the LPS of many eubacteria. It is believed that precursors of the methylated-deoxyhexoses traverse common early biosynthetic steps as nucleotide-monosaccharides. As a prelude to a full biosynthetic characterization, we present herein the results from bioinformatics-based, proteomics-supported predictions of the pathway for virenose synthesis. Alternative possibilities are considered which include both GDP-mannose and TDP-glucose as precursors. Conclusion We propose that biosynthesis of the unique C. burnetii biomarker, virenose, involves an early pathway similar to that of other C-3’-methylated deoxysugars which then diverges depending upon the nucleotide-carrier involved. The alternatives yield either the D- or L-enantiomers of virenose. Both pathways require five enzymatic steps, beginning with either glucose-6-phosphate or mannose-6-phosphate. Our in silico results comprise a model for virenose biosynthesis that can be directly tested. Definition of this pathway should facilitate the development of therapeutic agents useful for treatment of Q fever, as well as allowing improvements in the methods for diagnosing this highly infectious disease.
机译:背景伯氏柯氏杆菌是革兰氏阴性细菌,可引起人畜共患的Q型热。尽管它具有专一的细胞内生长习性,但它能够在宿主细胞外持续较长时间,并且可以抵抗大多数原核生物可能致命的环境条件。这些细胞外细菌是真核宿主遇到的感染阶段。细胞内形式已经进化为在酸化的亚寄生液泡中生长和复制。伯氏梭菌的外层包含复杂的脂多糖(LPS)组分,该组分包括独特的甲基化的6-脱氧己糖,肾上腺素。尽管作为伯氏梭菌的生物标志物可能很重要,但其生物合成途径仍然不清楚。结果6-脱氧己糖构成许多真细菌的LPS不可或缺的大家族。据信,甲基化的脱氧己糖的前体作为核苷酸单糖经过常见的早期生物合成步骤。作为全面生物合成表征的前奏,我们在此介绍来自基于蛋白质组学的蛋白质组学支持的生物信息学预测的结果。考虑了替代可能性,包括GDP-甘露糖和TDP-葡萄糖均作为前体。结论我们建议,独特的伯氏梭菌生物标志物,病毒糖的生物合成涉及一个早期途径,该途径与其他C-3′-甲基化脱氧糖相似,然后根据所涉及的核苷酸载体而发生分歧。替代方案产生了维尼糖的D-或L-对映体。两种途径都需要五个酶促步骤,从6-磷酸葡萄糖或6-磷酸甘露糖开始。我们的计算机模拟结果包括可以直接测试的病毒糖生物合成模型。该途径的定义应促进开发可用于治疗Q热的治疗剂,并允许改进诊断这种高度传染性疾病的方法。

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