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将通量分布分解为基因组尺度代谢网络中的基本通量模式。

Decomposing flux distributions into elementary flux modes in genome-scale metabolic networks.

机构信息

Department of Industrial and Systems Engineering, The Hong Kong Polytechnic University, Hung Hom, Hong Kong.

出版信息

Bioinformatics. 2011 Aug 15;27(16):2256-62. doi: 10.1093/bioinformatics/btr367. Epub 2011 Jun 17.

Abstract

MOTIVATION

Elementary flux mode (EFM) is a fundamental concept as well as a useful tool in metabolic pathway analysis. One important role of EFMs is that every flux distribution can be decomposed into a set of EFMs and a number of methods to study flux distributions originated from it. Yet finding such decompositions requires the complete set of EFMs, which is intractable in genome-scale metabolic networks due to combinatorial explosion.

RESULTS

In this article, we proposed an algorithm to decompose flux distributions into EFMs in genome-scale networks. It is an iterative scheme of a mixed integer linear program. Unlike previous optimization models to find pathways, any feasible solutions can become EFMs in our algorithm. This advantage enables the algorithm to approximate the EFM of largest contribution to an objective reaction in a flux distribution. Our algorithm is able to find EFMs of flux distributions with complex structures, closer to the realistic case in which a cell is subject to various constraints. A case of Escherichia coli growth in the Lysogeny broth (LB) medium containing various carbon sources was studied. Essential metabolites and their syntheses were located. Information on the contribution of each carbon source not obvious from the apparent flux distribution was also revealed. Our work further confirms the utility of finding EFMs by optimization models in genome-scale metabolic networks.

CONTACT

joshua.chan@connect.polyu.hk

SUPPLEMENTARY INFORMATION

Supplementary data are available at Bioinformatics online.

摘要

动机

基本通量模式 (EFM) 是代谢途径分析中的一个基本概念和有用工具。EFM 的一个重要作用是,每个通量分布都可以分解为一组 EFM 和一些源于它的通量分布研究方法。然而,找到这样的分解需要完整的 EFM 集,由于组合爆炸,在基因组规模的代谢网络中这是难以处理的。

结果

本文提出了一种在基因组规模网络中将通量分布分解为 EFM 的算法。它是一个混合整数线性规划的迭代方案。与之前寻找途径的优化模型不同,我们的算法中的任何可行解都可以成为 EFM。这个优势使算法能够在通量分布中接近目标反应的最大贡献 EFM。我们的算法能够找到具有复杂结构的通量分布的 EFM,更接近细胞受到各种约束的实际情况。以含有各种碳源的 Lysogeny 肉汤 (LB) 培养基中大肠杆菌的生长为例进行了研究。定位了必需代谢物及其合成。还揭示了从明显的通量分布中不易看出的每个碳源的贡献信息。我们的工作进一步证实了在基因组规模代谢网络中通过优化模型寻找 EFM 的实用性。

联系方式

joshua.chan@connect.polyu.hk

补充信息

补充数据可在“Bioinformatics”在线获取。

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