%0 Journal Article %A Ganapathy, Uday %A Marrero, Joeli %A Calhoun, Susannah %A Eoh, Hyungjin %A de Carvalho, Luiz Pedro Sorio %A Rhee, Kyu %A Ehrt, Sabine %D 2020 %T Two enzymes with redundant fructose bisphosphatase activity sustain gluconeogenesis and virulence in Mycobacterium tuberculosis %U https://crick.figshare.com/articles/journal_contribution/Two_enzymes_with_redundant_fructose_bisphosphatase_activity_sustain_gluconeogenesis_and_virulence_in_Mycobacterium_tuberculosis/12727637 %2 https://crick.figshare.com/ndownloader/files/24093038 %K Fructose-Bisphosphatase %K Gluconeogenesis %K Lithium %K Mycobacterium tuberculosis %K Virulence %K de Carvalho MC_UP_A253_1111 %X The human pathogen Mycobacterium tuberculosis (Mtb) likely utilizes host fatty acids as a carbon source during infection. Gluconeogenesis is essential for the conversion of fatty acids into biomass. A rate-limiting step in gluconeogenesis is the conversion of fructose 1,6-bisphosphate to fructose 6-phosphate by a fructose bisphosphatase (FBPase). The Mtb genome contains only one annotated FBPase gene, glpX. Here we show that, unexpectedly, an Mtb mutant lacking GLPX grows on gluconeogenic carbon sources and has detectable FBPase activity. We demonstrate that the Mtb genome encodes an alternative FBPase (GPM2, Rv3214) that can maintain gluconeogenesis in the absence of GLPX. Consequently, deletion of both GLPX and GPM2 is required for disruption of gluconeogenesis and attenuation of Mtb in a mouse model of infection. Our work affirms a role for gluconeogenesis in Mtb virulence and reveals previously unidentified metabolic redundancy at the FBPase-catalysed reaction step of the pathway. %I The Francis Crick Institute