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An Inhibitor of Exported Mycobacterium tuberculosis Glutamine Synthetase Selectively Blocks the Growth of Pathogenic Mycobacteria in Axenic Culture and in Human Monocytes: Extracellular Proteins as Potential Novel Drug Targets

机译:出口的结核分枝杆菌谷氨酰胺合成酶的抑制剂选择性地阻止病原性分枝杆菌在轴突培养和人单核细胞中的生长:细胞外蛋白作为潜在的新型药物靶标

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摘要

Mycobacterium tuberculosis and other pathogenic mycobacteria export abundant quantities of proteins into their extracellular milieu when growing either axenically or within phagosomes of host cells. One major extracellular protein, the enzyme glutamine synthetase, is of particular interest because of its link to pathogenicity. Pathogenic mycobacteria, but not nonpathogenic mycobacteria, export large amounts of this protein. Interestingly, export of the enzyme is associated with the presence of a poly-l-glutamate/glutamine structure in the mycobacterial cell wall. In this study, we investigated the influence of glutamine synthetase inhibitors on the growth of pathogenic and nonpathogenic mycobacteria and on the poly-l-glutamate/glutamine cell wall structure.
机译:结核分枝杆菌和其他致病性分枝杆菌在轴突生长或在宿主细胞吞噬体内生长时,会将大量蛋白质输出到其细胞外环境中。谷氨酰胺合成酶是一种主要的细胞外蛋白,因为它与致病性有关,因此特别受到关注。致病性分枝杆菌,而非非致病性分枝杆菌,输出大量这种蛋白质。有趣的是,酶的输出与分枝杆菌细胞壁中聚-1-谷氨酸/谷氨酰胺结构的存在有关。在这项研究中,我们研究了谷氨酰胺合成酶抑制剂对致病性和非致病性分枝杆菌的生长以及对聚-1-谷氨酸/谷氨酰胺细胞壁结构的影响。

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  • 年度 1999
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  • 正文语种 {"code":"en","name":"English","id":9}
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