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薄层层析法分析分枝杆菌的脂类组成。

Analysis of the Lipid Composition of Mycobacteria by Thin Layer Chromatography.

机构信息

Departament de Genètica i de Microbiologia, Facultat de Biociències, Universitat Autònoma de Barcelona.

Departament de Genètica i de Microbiologia, Facultat de Biociències, Universitat Autònoma de Barcelona;

出版信息

J Vis Exp. 2021 Apr 16(170). doi: 10.3791/62368.

Abstract

Mycobacteria species can differ from one another in the rate of growth, presence of pigmentation, the colony morphology displayed on solid media, as well as other phenotypic characteristics. However, they all have in common the most relevant character of mycobacteria: its unique and highly hydrophobic cell wall. Mycobacteria species contain a membrane-covalent linked complex that includes arabinogalactan, peptidoglycan, and long-chains of mycolic acids with types that differ between mycobacteria species. Additionally, mycobacteria can also produce lipids that are located, non-covalently linked, on their cell surfaces, such as phthiocerol dimycocerosates (PDIM), phenolic glycolipids (PGL), glycopeptidolipids (GPL), acyltrehaloses (AT), or phosphatidil-inositol mannosides (PIM), among others. Some of them are considered virulence factors in pathogenic mycobacteria, or critical antigenic lipids in host-mycobacteria interaction. For these reasons, there is a significant interest in the study of mycobacterial lipids due to their application in several fields, from understanding their role in the pathogenicity of mycobacteria infections, to a possible implication as immunomodulatory agents for the treatment of infectious diseases and other pathologies such as cancer. Here, a simple approach to extract and analyze the total lipid content and the mycolic acid composition of mycobacteria cells grown in a solid medium using mixtures of organic solvents is presented. Once the lipid extracts are obtained, thin-layer chromatography (TLC) is performed to monitor the extracted compounds. The example experiment is performed with four different mycobacteria: the environmental fast-growing Mycolicibacterium brumae and Mycolicibacterium fortuitum, the attenuated slow-growing Mycobacterium bovis bacillus Calmette-Guérin (BCG), and the opportunistic pathogen fast-growing Mycobacterium abscessus, demonstrating that methods shown in the present protocol can be used to a wide range of mycobacteria.

摘要

分枝杆菌物种在生长速度、色素沉着、固体培养基上显示的菌落形态以及其他表型特征上可能存在差异。然而,它们都有一个分枝杆菌的共同特征:其独特的高度疏水性细胞壁。分枝杆菌物种含有一种膜共价连接的复合物,其中包括阿拉伯半乳聚糖、肽聚糖和长链分枝菌酸,这些酸的类型在分枝杆菌物种之间有所不同。此外,分枝杆菌还可以产生位于其细胞表面的非共价连接的脂质,例如 phthiocerol dimycocerosates (PDIM)、酚类糖脂 (PGL)、糖肽脂 (GPL)、酰基海藻糖 (AT) 或磷脂酰肌醇甘露糖苷 (PIM) 等。其中一些被认为是致病性分枝杆菌的毒力因子,或宿主分枝杆菌相互作用中的关键抗原性脂质。由于它们在几个领域的应用,如了解它们在分枝杆菌感染的致病性中的作用,以及作为治疗感染性疾病和其他疾病(如癌症)的免疫调节剂的可能性,因此对分枝杆菌脂质的研究具有重要意义。在这里,介绍了一种使用有机溶剂混合物从固体培养基中生长的分枝杆菌细胞中提取和分析总脂质含量和分枝菌酸组成的简单方法。一旦获得脂质提取物,就可以通过薄层层析 (TLC) 来监测提取的化合物。该示例实验使用了四种不同的分枝杆菌:环境中快速生长的分枝杆菌 Mycolicibacterium brumae 和分枝杆菌 Mycolicibacterium fortuitum、减毒缓慢生长的分枝杆菌 Mycobacterium bovis bacillus Calmette-Guérin (BCG) 和机会性致病菌快速生长的分枝杆菌 Mycobacterium abscessus,证明了本方案中所示的方法可用于广泛的分枝杆菌。

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