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Biology subjects

Niebel, B.

Publications and source records attributed to Niebel, B..

2 recordsLinked to original sources

Unbiased metabolic flux inference through combined thermodynamic and 13C flux analysis

ABSTRACTQuantification of cellular metabolic fluxes, for instance with 13C-metabolic flux analysis, is highly important for applied and fundamental metabolic research. A current challenge in 13C-flux analysis is that the available experimental data are usually insufficient to resolve metabolic fluxes in large metabolic networks without making assumptions on flux directions and reversibility. To infer metabolic fluxes in a more unbiased manner, we devised an approach that does not require such assumptions. The developed three-step approach integrates thermodynamics, metabolome, physiological data, and 13C labelling data, and involves a novel method to comprehensively sample the complex thermodynamically-constrained metabolic flux space. Applying our approach to budding yeast with its compartmentalised metabolism and parallel pathways, we could resolve metabolic fluxes in an unbiased manner, we obtained an uncertainty estimate for each flux, and we found novel flux patterns that until now had remained unknown, likely due to assumptions made in previous 13C flux analysis studies. We expect that our approach will be an important step forward to determine metabolic fluxes with improved accuracy in microorganisms and possibly also in more complex organisms.View Full Text

systems biology↗

Saccharomyces cerevisiae goes through distinct metabolic phases during its replicative lifespan

A comprehensive description of the phenotypic changes during cellular aging is key towards unraveling its causal forces. Using recently developed experimental tools, which previously had enabled us to map age related changes in proteome and transcriptome (Janssens et al., 2015), and model-based inference methods, here, we generated a comprehensive account of the metabolic changes during the entire replicative life of Saecharomyces cerevisiae. With age, we found decreasing metabolite levels, decreasing growth and substrate uptake rates accompanied by a switch from aerobic fermentation to a respiratory metabolism, with increased glycerol and acetate production. The identification of intracellular metabolic fluxes revealed an increase in redox cofactor turnover, likely to combat the increased production of reactive oxygen species. The identified metabolic changes possibly reflect a dynamic adaptation to the age-associated, non- homeostatic increase in volume. With metabolism being an important factor of the cellular phenotype, this work complements our recent mapping of the transcriptomic and proteomic changes towards a holistic description of the cellular processes during aging.

cell biology↗