Consistency Analysis of Genome-Scale Models of Bacterial Metabolism: A Metamodel Approach

被引:7
作者
Ponce-de-Leon, Miguel [1 ]
Calle-Espinosa, Jorge [1 ]
Pereto, Juli [2 ,3 ]
Montero, Francisco [1 ]
机构
[1] Univ Complutense Madrid, Fac Ciencias Quim, Dept Bioquim & Biol Mol 1, Madrid 28045, Spain
[2] Univ Valencia, Dept Bioquim & Biol Mol, Paterna 46980, Spain
[3] Univ Valencia, Inst Cavanilles Biodiversitat & Biol Evolut, Paterna 46980, Spain
来源
PLOS ONE | 2015年 / 10卷 / 12期
关键词
FLUX COUPLING ANALYSIS; NETWORK RECONSTRUCTION; PATHWAY DATABASES; ORPHAN ENZYMES; SYSTEMS; ANNOTATION; OPTIMIZATION; GENERATION; PREDICTION; BALANCE;
D O I
10.1371/journal.pone.0143626
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Genome-scale metabolic models usually contain inconsistencies that manifest as blocked reactions and gap metabolites. With the purpose to detect recurrent inconsistencies in metabolic models, a large-scale analysis was performed using a previously published dataset of 130 genome-scale models. The results showed that a large number of reactions (similar to 22%) are blocked in all the models where they are present. To unravel the nature of such inconsistencies a metamodel was construed by joining the 130 models in a single network. This metamodel was manually curated using the unconnected modules approach, and then, it was used as a reference network to perform a gap-filling on each individual genome-scale model. Finally, a set of 36 models that had not been considered during the construction of the metamodel was used, as a proof of concept, to extend the metamodel with new biochemical information, and to assess its impact on gap-filling results. The analysis performed on the metamodel allowed to conclude: 1) the recurrent inconsistencies found in the models were already present in the metabolic database used during the reconstructions process; 2) the presence of inconsistencies in a metabolic database can be propagated to the reconstructed models; 3) there are reactions not manifested as blocked which are active as a consequence of some classes of artifacts, and; 4) the results of an automatic gap-filling are highly dependent on the consistency and completeness of the metamodel or metabolic database used as the reference network. In conclusion the consistency analysis should be applied to metabolic databases in order to detect and fill gaps as well as to detect and remove artifacts and redundant information.
引用
收藏
页数:22
相关论文
共 62 条
[11]   Competitive and cooperative metabolic interactions in bacterial communities [J].
Freilich, Shiri ;
Zarecki, Raphy ;
Eilam, Omer ;
Segal, Ella Shtifman ;
Henry, Christopher S. ;
Kupiec, Martin ;
Gophna, Uri ;
Sharan, Roded ;
Ruppin, Eytan .
NATURE COMMUNICATIONS, 2011, 2
[12]   A Bayesian method for identifying missing enzymes in predicted metabolic pathway databases [J].
Green, ML ;
Karp, PD .
BMC BIOINFORMATICS, 2004, 5 (1)
[13]  
Hagberg A. A., 2008, P 7 PYTH SCI C SCIPY, P11, DOI DOI 10.1016/J.JELECTROCARD.2010.09.003
[14]   WHOLE-GENOME METABOLIC NETWORK RECONSTRUCTION AND CONSTRAINT-BASED MODELING [J].
Haggart, Charles R. ;
Bartell, Jennifer A. ;
Saucerman, Jeffrey J. ;
Papin, Jason A. .
METHODS IN ENZYMOLOGY, VOL 500: METHODS IN SYSTEMS BIOLOGY, 2011, 500 :411-433
[15]   'Unknown' proteins and 'orphan' enzymes: the missing half of the engineering parts list - and how to find it [J].
Hanson, Andrew D. ;
Pribat, Anne ;
Waller, Jeffrey C. ;
de Crecy-Lagard, Valerie .
BIOCHEMICAL JOURNAL, 2010, 425 :1-11
[16]   The modelling of metabolic systems. Structure, control and optimality [J].
Heinrich, R ;
Schuster, S .
BIOSYSTEMS, 1998, 47 (1-2) :61-77
[17]   High-throughput generation, optimization and analysis of genome-scale metabolic models [J].
Henry, Christopher S. ;
DeJongh, Matthew ;
Best, Aaron A. ;
Frybarger, Paul M. ;
Linsay, Ben ;
Stevens, Rick L. .
NATURE BIOTECHNOLOGY, 2010, 28 (09) :977-U22
[18]   The systems biology markup language (SBML):: a medium for representation and exchange of biochemical network models [J].
Hucka, M ;
Finney, A ;
Sauro, HM ;
Bolouri, H ;
Doyle, JC ;
Kitano, H ;
Arkin, AP ;
Bornstein, BJ ;
Bray, D ;
Cornish-Bowden, A ;
Cuellar, AA ;
Dronov, S ;
Gilles, ED ;
Ginkel, M ;
Gor, V ;
Goryanin, II ;
Hedley, WJ ;
Hodgman, TC ;
Hofmeyr, JH ;
Hunter, PJ ;
Juty, NS ;
Kasberger, JL ;
Kremling, A ;
Kummer, U ;
Le Novère, N ;
Loew, LM ;
Lucio, D ;
Mendes, P ;
Minch, E ;
Mjolsness, ED ;
Nakayama, Y ;
Nelson, MR ;
Nielsen, PF ;
Sakurada, T ;
Schaff, JC ;
Shapiro, BE ;
Shimizu, TS ;
Spence, HD ;
Stelling, J ;
Takahashi, K ;
Tomita, M ;
Wagner, J ;
Wang, J .
BIOINFORMATICS, 2003, 19 (04) :524-531
[19]   Evolutionary Conservation of Bacterial Essential Metabolic Genes across All Bacterial Culture Media [J].
Ish-Am, Oren ;
Kristensen, David M. ;
Ruppin, Eytan .
PLOS ONE, 2015, 10 (04)
[20]   Organization of genes for tetrapyrrole biosynthesis in Gram-positive bacteria [J].
Johansson, P ;
Hederstedt, L .
MICROBIOLOGY-SGM, 1999, 145 :529-538