Metabolic reconstruction of the archaeon methanogen Methanosarcina Acetivorans

被引:41
|
作者
Kumar, Vinay Satish [2 ]
Ferry, James G. [3 ]
Maranas, Costas D. [1 ]
机构
[1] Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
[2] Joint BioEnergy Inst, Emeryville, CA 94608 USA
[3] Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
关键词
GENOME; EVOLUTION; FRAMEWORK; GENES; MAZEI; LIFE;
D O I
10.1186/1752-0509-5-28
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Methanogens are ancient organisms that are key players in the carbon cycle accounting for about one billion tones of biological methane produced annually. Methanosarcina acetivorans, with a genome size of similar to 5.7 mb, is the largest sequenced archaeon methanogen and unique amongst the methanogens in its biochemical characteristics. By following a systematic workflow we reconstruct a genome-scale metabolic model for M. acetivorans. This process relies on previously developed computational tools developed in our group to correct growth prediction inconsistencies with in vivo data sets and rectify topological inconsistencies in the model. Results: The generated model iVS941 accounts for 941 genes, 705 reactions and 708 metabolites. The model achieves 93.3% prediction agreement with in vivo growth data across different substrates and multiple gene deletions. The model also correctly recapitulates metabolic pathway usage patterns of M. acetivorans such as the indispensability of flux through methanogenesis for growth on acetate and methanol and the unique biochemical characteristics under growth on carbon monoxide. Conclusions: Based on the size of the genome-scale metabolic reconstruction and extent of validated predictions this model represents the most comprehensive up-to-date effort to catalogue methanogenic metabolism. The reconstructed model is available in spreadsheet and SBML formats to enable dissemination.
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页数:10
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