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Integration of biomass functions of genome-scale metabolic models with experimental data reveals universally essential cofactors in prokaryotes

机译:基因组规模代谢模型的生物量功能与实验数据的整合揭示了原核生物中普遍必需的辅因子

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摘要

Knowledge of the core biochemical composition of the cell is critical for genome-scale metabolic modelling. In order to identify the universal core organic cofactors for prokaryotes, we performed a detailed analysis of biomass objective functions (BOFs) of 71 manually curated genome-scale prokaryotic models. These were then compared and integrated with the ModelSEED framework for biomass composition, experimental data on gene essentiality, curated enzyme-cofactor association data and a comprehensive survey of the literature. Surprisingly, no cofactor was present in all the BOFs analysed, including the important redox cofactor nicotinamide adenine dinucleotide (NAD) or its derivatives. Our results indicate not only the redox cofactors but also others such as coenzyme A, flavins and thiamin as universally essential for prokaryotes and therefore as important to include in the BOFs of future genome-scale models of prokaryotic organisms.
机译:了解细胞的核心生化组成对于基因组规模的代谢建模至关重要。为了鉴定原核生物的通用核心有机辅因子,我们对71种手动选择的基因组规模原核生物模型的生物量目标函数(BOF)进行了详细分析。然后将这些进行比较,并与ModelSEED框架的生物量组成,基因必要性的实验数据,精选的酶-辅因子关联数据和文献综合调查相集成。出乎意料的是,在所有分析的BOF中都不存在辅助因子,包括重要的氧化还原辅助因子烟酰胺腺嘌呤二核苷酸(NAD)或其衍生物。我们的结果表明,不仅氧化还原辅助因子,而且其他辅酶A,黄素和硫胺素对于原核生物也是普遍必需的,因此对于将其包含在未来原核生物基因组规模模型的BOF中同样重要。

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