Systematizing the Generation of Missing Metabolic Knowledge

被引:110
作者
Orth, Jeffrey D. [1 ]
Palsson, Bernhard O. [1 ]
机构
[1] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
gap-filling; gene annotation; growmatch; metabolic network reconstruction; SMILEY; ESCHERICHIA-COLI K-12; PATHWAY; RECONSTRUCTION; GENES; ENZYMES; IDENTIFICATION; CAPABILITIES; PREDICTION; GENOMICS; SEED;
D O I
10.1002/bit.22844
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Genome-scale metabolic network reconstructions are built from all of the known metabolic reactions and genes in a target organism. However, since our knowledge of any organism is incomplete, these network reconstructions contain gaps. Reactions may be missing, resulting in dead-ends in pathways, while unknown gene products may catalyze known reactions. New computational methods that analyze data, such as growth phenotypes or gene essentiality, in the context of genome-scale metabolic networks, have been developed to predict these missing reactions or genes likely to fill these knowledge gaps. A growing number of experimental studies are appearing that address these computational predictions, leading to discovery of new metabolic capabilities in the target organism. Gap-filling methods can thus be used to improve metabolic network models while simultaneously leading to discovery of new metabolic gene functions. Biotechnol. Bioeng. 2010; 107: 403-412. (C) 2010 Wiley Periodicals, Inc.
引用
收藏
页码:403 / 412
页数:10
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