Our aim was to determine whether fixation of inorganic carbon (C(i)), due to phosphoenolpyruvate carboxylase activity, is limited by the availability of C(i) in the cytoplasm of maize (Zea mays L.) root tips. Rates of C(i) uptake and metabolism were measured during K2SO4 treatment, which stimulates dark C(i) fixation. C-13(i) uptake was followed by C-13-nuclear magnetic resonance (NMR); 5 millimolar K2SO4 had no significant effect on C-13(i) influx. The contribution of respiratory CO2 production to cytoplasmic HCO3- was measured using in vivo C-13-NMR and H-1-NMR of cell extracts; K2SO4 treatment had no effect on respiratory CO2 production. The concentration of cytoplasmic HCO3- was estimated to be approximately 11 millimolar, again with K2SO4 having no significant effect. These experiments allowed us to determine the extent to which extracellularly supplied C-14(i) was diluted in the cytoplasm by respiratory CO2 and thereby measure phosphoenolpyruvate (PEP) carboxylase activity in vivo using C-14(i). PEP carboxylase activity in root tips was enhanced approximately 70% over controls within 12 minutes of the addition of 5 millimolar K2SO4. The activity of carbonic anhydrase, which provides PEP carboxylase with C(i), was determined by saturation transfer C-13-NMR to be more than 200 times that of PEP carboxylase in vivo. The regulation of PEP carboxylase in K2SO4-treated roots is discussed.