ArticleBMC systems biology2015
Impact of kinetic isotope effects in isotopic studies of metabolic systems.
Article in BMC systems biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
What it found
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
13 citing papers in PubMed, 34 citations in OpenAlex.
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- Autotrophic and mixotrophic metabolism of an anammox bacterium revealed by in vivoThe ISME journal · 2021Article
- ScalaFlux: A scalable approach to quantify fluxes in metabolic subnetworks.PLoS computational biology · 2020Article
- DeltaMS: a tool to track isotopologues in GC- and LC-MS data.Metabolomics : Official journal of the Metabolomic Society · 2018Article
- The rate of lactate production from glucose in hearts is not altered by per-deuteration of glucose.Journal of magnetic resonance (San Diego, Calif. : 1997) · 2017Article
- Modeling the dynamics of mouse iron body distribution: hepcidin is necessary but not sufficient.BMC systems biology · 2017Article
- KineticScientific reports · 2017Article
- Shifts in rotifer life history in response to stable isotope enrichment: testing theories of isotope effects on organismal growth.Royal Society open science · 2017Article
- Acetate fluxes in Escherichia coli are determined by the thermodynamic control of the Pta-AckA pathway.Scientific reports · 2017Article
- Quantification of Microbial Phenotypes.Metabolites · 2016Review
- Evolution of E. coli on [U-13C]Glucose Reveals a Negligible Isotopic Influence on Metabolism and Physiology.PloS one · 2016Article
Corrections and comments
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Authors and funding
3 authors at 2 institutions in 2 countries.
Funding
Abstract
backgroundIsotope labeling experiments (ILEs) are increasingly used to investigate the functioning of metabolic systems. Some enzymes are subject to kinetic isotope effects (KIEs) which modulate reaction rates depending on the isotopic composition of their substrate(s). KIEs may therefore affect both the propagation of isotopes through metabolic networks and their operation, and ultimately jeopardize the biological value of ILEs. However, the actual impact of KIEs on metabolism has never been investigated at the system level.
resultsFirst, we developed a framework which integrates KIEs into kinetic and isotopic models of metabolism, thereby accounting for their system-wide effects on metabolite concentrations, metabolic fluxes, and isotopic patterns. Then, we applied this framework to assess the impact of KIEs on the central carbon metabolism of Escherichia coli in the context of (13)C-ILEs, under different situations commonly encountered in laboratories. Results showed that the impact of KIEs strongly depends on the label input and on the variable considered but is significantly lower than expected intuitively from measurements on isolated enzymes. The global robustness of both the metabolic operation and isotopic patterns largely emerge from intrinsic properties of metabolic networks, such as the distribution of control across the network and bidirectional isotope exchange.
conclusionsThese results demonstrate the necessity of investigating the impact of KIEs at the level of the entire system, contradict previous hypotheses that KIEs would have a strong effect on isotopic distributions and on flux determination, and strengthen the biological value of (13)C-ILEs. The proposed modeling framework is generic and can be used to investigate the impact of all the isotopic tracers ((2)H, (13)C, (15)N, (18)O, etc.) on different isotopic datasets and metabolic systems. By allowing the integration of isotopic and metabolomics data collected under stationary and/or non-stationary conditions, it may also assist interpretations of ILEs and facilitate the development of more accurate kinetic models with improved explicative and predictive capabilities.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.