• DOI:10.1002/BIT.21632
• Corpus ID: 8240039

An elementary metabolite unit (EMU) based method of isotopically nonstationary flux analysis

@article{Young2008AnEM,
  title={An elementary metabolite unit (EMU) based method of isotopically nonstationary flux analysis},
  author={Jamey D. Young and Jason Walther and Maciek R. Antoniewicz and Hyuntae Yoo and Gregory Stephanopoulos},
  journal={Biotechnology and Bioengineering},
  year={2008},
  volume={99}
}

• Jamey D. Young, Jason Walther, +2 authors G. Stephanopoulos
• Published 15 February 2008
• Engineering, Biology
• Biotechnology and Bioengineering

Nonstationary metabolic flux analysis (NMFA) is at present a very computationally intensive exercise, especially for large reaction networks. We applied elementary metabolite unit (EMU) theory to NMFA, dramatically reducing computational difficulty. We also introduced block decoupling, a new method that systematically and comprehensively divides EMU systems of equations into smaller subproblems to further reduce computational difficulty. These improvements led to a 5000‐fold reduction in simulation times, enabling an entirely new and more complicated set of problems to be analyzed with NMFA. We simulated a series of nonstationary and stationary GC/MS measurements for a large E. coli network that was then used to estimate parameters and their associated confidence intervals. We found that fluxes could be successfully estimated using only nonstationary labeling data and external flux measurements. Addition of near‐stationary and stationary time points increased the precision of most parameters. Contrary to prior reports, the precision of nonstationary estimates proved to be comparable to the precision of estimates based solely on stationary data. Finally, we applied EMU‐based NMFA to experimental nonstationary measurements taken from brown adipocytes and successfully estimated fluxes and some metabolite concentrations. By using NFMA instead of traditional MFA, the experiment required only 6 h instead of 50 (the time necessary for most metabolite labeling to reach 99% of isotopic steady state). Biotechnol. Bioeng. 2008;99: 686–699. © 2007 Wiley Periodicals, Inc.