Figure 3.
pH-dependent effects on glucose uptake in X. laevis oocytes injected with cRNA of B. bruxellensisgenes encoding glucose transporters. Oocytes were incubated 1 hour in 0.1 mM glucose buffer at the indicated pH. Injection of cRNA GFP was used as negative controls to account for endogenous glucose uptake. The assays were performed at least in triplicate. Error bars indicate one standard deviation.