FiatFlux – a software for metabolic flux analysis from <sup>13</sup>C-glucose experiments

<p>Abstract</p> <p>Background</p> <p>Quantitative knowledge of intracellular fluxes is important for a comprehensive characterization of metabolic networks and their functional operation. In contrast to direct assessment of metabolite concentrations, in vivo metabolite...

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Main Authors: Fischer Eliane, Zamboni Nicola, Sauer Uwe
Format: Article
Language:English
Published: BMC 2005-08-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/6/209
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spelling doaj-fc7b0cada99246788f06b183c50382ee2020-11-25T02:09:28ZengBMCBMC Bioinformatics1471-21052005-08-016120910.1186/1471-2105-6-209FiatFlux – a software for metabolic flux analysis from <sup>13</sup>C-glucose experimentsFischer ElianeZamboni NicolaSauer Uwe<p>Abstract</p> <p>Background</p> <p>Quantitative knowledge of intracellular fluxes is important for a comprehensive characterization of metabolic networks and their functional operation. In contrast to direct assessment of metabolite concentrations, in vivo metabolite fluxes must be inferred indirectly from measurable quantities in <sup>13</sup>C experiments. The required experience, the complicated network models, large and heterogeneous data sets, and the time-consuming set-up of highly controlled experimental conditions largely restricted metabolic flux analysis to few expert groups. A conceptual simplification of flux analysis is the analytical determination of metabolic flux ratios exclusively from MS data, which can then be used in a second step to estimate absolute in vivo fluxes.</p> <p>Results</p> <p>Here we describe the user-friendly software package FiatFlux that supports flux analysis for non-expert users. In the first module, ratios of converging fluxes are automatically calculated from GC-MS-detected <sup>13</sup>C-pattern in protein-bound amino acids. Predefined fragmentation patterns are automatically identified and appropriate statistical data treatment is based on the comparison of redundant information in the MS spectra. In the second module, absolute intracellular fluxes may be calculated by a <sup>13</sup>C-constrained flux balancing procedure that combines experimentally determined fluxes in and out of the cell and the above flux ratios. The software is preconfigured to derive flux ratios and absolute in vivo fluxes from [1-<sup>13</sup>C] and [U-<sup>13</sup>C]glucose experiments and GC-MS analysis of amino acids for a variety of microorganisms.</p> <p>Conclusion</p> <p>FiatFlux is an intuitive tool for quantitative investigations of intracellular metabolism by users that are not familiar with numerical methods or isotopic tracer experiments. The aim of this open source software is to enable non-specialists to adapt the software to their specific scientific interests, including other <sup>13</sup>C-substrates, labeling mixtures, and organisms.</p> http://www.biomedcentral.com/1471-2105/6/209
collection DOAJ
language English
format Article
sources DOAJ
author Fischer Eliane
Zamboni Nicola
Sauer Uwe
spellingShingle Fischer Eliane
Zamboni Nicola
Sauer Uwe
FiatFlux – a software for metabolic flux analysis from <sup>13</sup>C-glucose experiments
BMC Bioinformatics
author_facet Fischer Eliane
Zamboni Nicola
Sauer Uwe
author_sort Fischer Eliane
title FiatFlux – a software for metabolic flux analysis from <sup>13</sup>C-glucose experiments
title_short FiatFlux – a software for metabolic flux analysis from <sup>13</sup>C-glucose experiments
title_full FiatFlux – a software for metabolic flux analysis from <sup>13</sup>C-glucose experiments
title_fullStr FiatFlux – a software for metabolic flux analysis from <sup>13</sup>C-glucose experiments
title_full_unstemmed FiatFlux – a software for metabolic flux analysis from <sup>13</sup>C-glucose experiments
title_sort fiatflux – a software for metabolic flux analysis from <sup>13</sup>c-glucose experiments
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2005-08-01
description <p>Abstract</p> <p>Background</p> <p>Quantitative knowledge of intracellular fluxes is important for a comprehensive characterization of metabolic networks and their functional operation. In contrast to direct assessment of metabolite concentrations, in vivo metabolite fluxes must be inferred indirectly from measurable quantities in <sup>13</sup>C experiments. The required experience, the complicated network models, large and heterogeneous data sets, and the time-consuming set-up of highly controlled experimental conditions largely restricted metabolic flux analysis to few expert groups. A conceptual simplification of flux analysis is the analytical determination of metabolic flux ratios exclusively from MS data, which can then be used in a second step to estimate absolute in vivo fluxes.</p> <p>Results</p> <p>Here we describe the user-friendly software package FiatFlux that supports flux analysis for non-expert users. In the first module, ratios of converging fluxes are automatically calculated from GC-MS-detected <sup>13</sup>C-pattern in protein-bound amino acids. Predefined fragmentation patterns are automatically identified and appropriate statistical data treatment is based on the comparison of redundant information in the MS spectra. In the second module, absolute intracellular fluxes may be calculated by a <sup>13</sup>C-constrained flux balancing procedure that combines experimentally determined fluxes in and out of the cell and the above flux ratios. The software is preconfigured to derive flux ratios and absolute in vivo fluxes from [1-<sup>13</sup>C] and [U-<sup>13</sup>C]glucose experiments and GC-MS analysis of amino acids for a variety of microorganisms.</p> <p>Conclusion</p> <p>FiatFlux is an intuitive tool for quantitative investigations of intracellular metabolism by users that are not familiar with numerical methods or isotopic tracer experiments. The aim of this open source software is to enable non-specialists to adapt the software to their specific scientific interests, including other <sup>13</sup>C-substrates, labeling mixtures, and organisms.</p>
url http://www.biomedcentral.com/1471-2105/6/209
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