## Abstract Metabolic flux analysis (MFA) is widely used to quantify metabolic pathway activity. Typical applications involve isotopically labeled substrates, which require both metabolic and isotopic steady states for simplified data analysis. For bacterial systems, these steady states are readily
Identification of optimal measurement sets for complete flux elucidation in metabolic flux analysis experiments
✍ Scribed by YoungJung Chang; Patrick F. Suthers; Costas D. Maranas
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 521 KB
- Volume
- 100
- Category
- Article
- ISSN
- 0006-3592
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Metabolic flux analysis (MFA) methods use external flux and isotopic measurements to quantify the magnitude of metabolic flows in metabolic networks. A key question in this analysis is choosing a set of measurements that is capable of yielding a unique flux distribution (identifiability). In this article, we introduce an optimization‐based framework that uses incidence structure analysis to determine the smallest (or most cost‐effective) set of measurements leading to complete flux elucidation. This approach relies on an integer linear programming formulation OptMeas that allows for the measurement of external fluxes and the complete (or partial) enumeration of the isotope forms of metabolites without requiring any of these to be chosen in advance. We subsequently query and refine the measurement sets suggested by OptMeas for identifiability and optimality. OptMeas is first tested on small to medium‐size demonstration examples. It is subsequently applied to a large‐scale E. coli isotopomer mapping model with more than 17,000 isotopomers. A number of additional measurements are identified leading to maximum flux elucidation in an amorphadiene producing E. coli strain. Biotechnol. Biotechnol. Bioeng. 2008;100: 1039–1049. © 2008 Wiley Periodicals, Inc.
📜 SIMILAR VOLUMES
A detailed stoichiometric model was developed for growth and penicillin-G production in Penicillium chrysogenum. From an a priori metabolic flux analysis using this model it appeared that penicillin production requires significant changes in fluxes through the primary metabolic pathways. This is bro
The measurement of uptake and secretion rates is often not sufficient to allow the calculation of all internal metabolic fluxes. Measurements of internal fluxes are needed and these additional measurements are used in conjunction with mass-balance equations to calculate the complete metabolic flux m