$$\Akt inhibitor beginaligned \textdpm = & AZD4547 order V_\textDI14C \left( f_\textCO_2 \right)\left( \alpha_1 t + \left( \Delta \textSA_\textCO_2 / \textSA_\textDIC \right)\left( 1 – e^ – \alpha_1 t \right) \right) \mathord\left/ \vphantom \left( \alpha_1 t + \left( \Delta \textSA_\textCO_2 / \textSA_\textDIC \right)\left( 1 – e^ – \alpha_1 t \right) \right) \alpha_1 \right. \kern-0pt \alpha_1

+ V_\textDI14C \left( 1 – f_\textCO_2 \right)\left( \alpha_2 t + \left( \Delta \textSA_\textHCO_3 / \textSA_\textDIC \right)\left( 1 – e^ – \alpha_2 t \right) \right) \mathord\left/ \vphantom \left( \alpha_2 t + \left( \Delta \textSA_\textHCO_3 / \textSA_\textDIC \right)\left( 1 – e^ – \alpha_2 t \right) \right) \alpha_2 \right. \kern-0pt \alpha_2 \\ \endaligned$$ (1) In this equation, V DI14C is the total rate of 14C uptake; \(f_\textCO_ 2 \) is the fraction of uptake attributable to CO2; α 1 and α 2 are the temperature-,

salinity-, and pH-dependent first-order rate constants for CO2 and HCO3 − hydration and dehydration, respectively; t is the time (s); \(\Delta \textSA_\textCO_2 \) and \(\Delta \textSA_\textHCO_3 \) are the differences between the initial and equilibrium 4SC-202 solubility dmso values of the specific activities of CO2 and HCO3 −, respectively; and SADIC is the specific activity of DIC. During steady-state photosynthesis, VDI14C and \(f_\textCO_ 2 \) are assumed to be constant so that changes in the instantaneous 14C uptake rate reflect only changes in the specific activity of CO2 and HCO3 −. In the present study, the 14C disequilibrium method was modified to enable measurements over a range of ecologically relevant pH values (7.90–8.70). In order to maintain a suitably large initial isotopic disequilibrium \(\left( ]# \right)\), the pH of the 14C spike solutions needs to be adjusted in conjunction with the pH of the assay buffer. We, thus, used either MES or HEPES buffers to set the pH of spike solutions over the range of 5.75–7.30 (see Table 2 for exact pH values of assay and spike buffers). For the assays, 10–30 × 106 cells were concentrated via gentle filtration over a polycarbonate filter (2 μm; Millipore, Billerica, MA, USA) to a final volume of 15 mL. During this filtration procedure, cells were kept in suspension, while the medium was gradually exchanged with buffered assay medium of the appropriate pH value. Assay media and spike buffers were prepared at least 1 day prior to the assay and stored in closed containers to avoid CO2 exchange and pH drift.