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多平台代谢组学特征分析揭示了 Rd KW20 的新型代谢产物和磷脂组成规律。

Multiplatform Metabolomics Characterization Reveals Novel Metabolites and Phospholipid Compositional Rules of Rd KW20.

机构信息

Centro de Metabolómica y Bioanálisis (CEMBIO), Facultad de Farmacia, Universidad San Pablo-CEU, CEU Universities, Urbanización Montepríncipe, 28660 Boadilla del Monte, Spain.

Departamento de Ciencias Médicas Básicas, Facultad de Medicina, Universidad San Pablo-CEU, CEU Universities, Urbanización Montepríncipe, 28660 Boadilla del Monte, Spain.

出版信息

Int J Mol Sci. 2023 Jul 6;24(13):11150. doi: 10.3390/ijms241311150.

Abstract

is a gram-negative bacterium of relevant clinical interest. Rd KW20 was the first organism to be sequenced and for which a genome-scale metabolic model (GEM) was developed. However, current GEMs are unable to capture several aspects of metabolome nature related to metabolite pools. To directly and comprehensively characterize the endometabolome of Rd KW20, we performed a multiplatform MS-based metabolomics approach combining LC-MS, GC-MS and CE-MS. We obtained direct evidence of 15-20% of the endometabolome present in current GEMs and showed that polar metabolite pools are interconnected through correlating metabolite islands. Notably, we obtained high-quality evidence of 18 metabolites not previously included in GEMs, including the antimicrobial metabolite cyclo(Leu-Pro). Additionally, we comprehensively characterized and evaluated the quantitative composition of the phospholipidome of , revealing that the fatty acyl chain composition is largely independent of the lipid class, as well as that the probability distribution of phospholipids is mostly related to the conditional probability distribution of individual acyl chains. This finding enabled us to provide a rationale for the observed phospholipid profiles and estimate the abundance of low-level species, permitting the expansion of the phospholipidome characterization through predictive probabilistic modelling.

摘要

是一种具有相关临床意义的革兰氏阴性菌。Rd KW20 是第一个被测序的生物体,并且为其开发了基因组规模的代谢模型 (GEM)。然而,当前的 GEM 无法捕捉到与代谢物库相关的代谢组学性质的几个方面。为了直接和全面地表征 Rd KW20 的内代谢组,我们采用了一种基于 MS 的多平台代谢组学方法,结合了 LC-MS、GC-MS 和 CE-MS。我们获得了当前 GEM 中存在的内代谢组的 15-20%的直接证据,并表明通过关联代谢物岛,极性代谢物库相互连接。值得注意的是,我们获得了 18 种以前未包含在 GEM 中的代谢物的高质量证据,包括抗菌代谢物环(亮氨酸-脯氨酸)。此外,我们全面地表征和评估了 Rd 的磷脂组的定量组成,揭示了脂肪酸酰基链组成在很大程度上独立于脂质类别,以及磷脂的概率分布主要与单个酰基链的条件概率分布有关。这一发现使我们能够为观察到的磷脂谱提供合理的解释,并估计低丰度物种的丰度,从而通过预测概率建模扩展磷脂组的特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1700/10342370/48de622c7090/ijms-24-11150-g001.jpg

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