2008 Annual Meeting
(5cu) Genome-Scale Model of a Minimal Organism: Mycoplasma genitalium
Author
Here, I present a systematic approach for the construction and curation of a genome-scale in silico metabolic model for M. genitalium. Key challenges included estimation of biomass composition, handling of enzymes with broad specificities and the lack of a defined medium. Computational tools were subsequently employed to identify and resolve connectivity gaps in the model as well as growth prediction inconsistencies with gene essentiality experimental data. The curated model, M. genitalium iPS189 (189 genes, 264 reactions, 276 metabolites) was 87% accurate in recapitulating in vivo gene essentiality results for M. genitalium. Approaches and tools described herein provide a roadmap for the automated construction of in silico metabolic models of other organisms.
Furthermore, this curated metabolic reconstruction allows for the rational design of a defined culture medium and an in silico exploration of the minimal number (and alternatives) of metabolic genes required for growth.