Further developments towards a genome-scale metabolic model of yeast

Paul D. Dobson(University of Manchester), Kieran Smallbone(University of Manchester), Daniel Jameson(University of Manchester), Evangelos Simeonidis(University of Manchester), Karin Lanthaler(University of Manchester), Pınar Pir(University of Cambridge), Chuan Lü(Aberystwyth University), Neil Swainston(University of Manchester), Warwick B. Dunn(University of Manchester), Paul G. Fisher(University of Manchester), Duncan Hull(University of Manchester), Marie Brown(University of Manchester), Olusegun Oshota(University of Manchester), Natalie Stanford(University of Manchester), Douglas B. Kell(University of Manchester), Ross D. King(Aberystwyth University), Stephen G. Oliver(University of Cambridge), Robert Stevens(University of Manchester), Pedro Mendes(University of Manchester)
BMC Systems Biology
October 28, 2010
Cited by 113Open Access
Full Text

Abstract

BACKGROUND: To date, several genome-scale network reconstructions have been used to describe the metabolism of the yeast Saccharomyces cerevisiae, each differing in scope and content. The recent community-driven reconstruction, while rigorously evidenced and well annotated, under-represented metabolite transport, lipid metabolism and other pathways, and was not amenable to constraint-based analyses because of lack of pathway connectivity. RESULTS: We have expanded the yeast network reconstruction to incorporate many new reactions from the literature and represented these in a well-annotated and standards-compliant manner. The new reconstruction comprises 1102 unique metabolic reactions involving 924 unique metabolites--significantly larger in scope than any previous reconstruction. The representation of lipid metabolism in particular has improved, with 234 out of 268 enzymes linked to lipid metabolism now present in at least one reaction. Connectivity is emphatically improved, with more than 90% of metabolites now reachable from the growth medium constituents. The present updates allow constraint-based analyses to be performed; viability predictions of single knockouts are comparable to results from in vivo experiments and to those of previous reconstructions. CONCLUSIONS: We report the development of the most complete reconstruction of yeast metabolism to date that is based upon reliable literature evidence and richly annotated according to MIRIAM standards. The reconstruction is available in the Systems Biology Markup Language (SBML) and via a publicly accessible database http://www.comp-sys-bio.org/yeastnet/.


Related Papers

No related papers found

Powered by citation graph analysis