Journal: Nature protocols
Article Title: A metabolic modeling platform for the Computation Of Microbial Ecosystems in Time and Space (COMETS)
doi: 10.1038/s41596-021-00593-3
Figure Lengend Snippet: Results from a chemostat simulation (Procedure 2), prepared with the Python toolbox, in which one strain unable to break down lactose (LCTStex_KO) receives galactose from a different strain (galE_KO) that can break lactose into glucose and galactose, but is unable to metabolize galactose. The medium environment was composed of a constant supply of lactose (lcts_e), ammonia, and trace nutrients. Galactose (gal_e) was not supplied externally but started being available in the environment as galE_KO grew. a) Biomass of the two strains over time (cycle indicates the current time step). b) Amounts of the key metabolites over time (ac_e = acetate, for_e = formate, gal_e = galactose, glyclt_e = glycolate, lcts_e = lactose, meoh_e = methanol, pppn_e = phenylpropanoate). Note that it is typical for limiting nutrients (here, lactose and galactose) to have near-zero concentrations in a chemostat. c) Fluxes of relevant exchange reactions in galE_KO, and d) LCTStex_KO (the prefix “EX_” indicates an exchange reaction, and the metabolites being exchanged with the environment are: ac_e = acetate, for_e = formate, gal_e = galactose, lcts_e = lactose, nh4_e = ammonia). Negative flux represents uptake, while positive flux is excretion.
Article Snippet: Here we simulate one such experiment with a genome-scale model of Prochlorococcus 84 , the most abundant marine photoautotroph. . Procedure 4: simulations including extracellular reactions This protocol demonstrates the capacity of COMETS to simulate reactions involving extracellular metabolites using the MATLAB toolbox.
Techniques: