Evidence for a physiological role of CO₂ in the regulation of photosynthetic electron transport in intact leaves

The effect of CO₂ upon photosynthetic electron transport was examined in wheat and maize leaves in order to establish whether CO₂ had a direct role in electron-transport regulation in vivo. When intercellular CO₂ was depleted a transient rise in chlorophyll fluorescence occurred which correlated with an increase in the reduction of the Photosystem II primary quinone acceptor, Q_A, and a decrease in CO₂ fixation rate. However, when intercellular CO₂ was reduced from an already low level (50 μmol·mol^-1) towards zero a substantial further reduction in Q_A occurred with little change in fluorescence or CO₂ fixation. In very low intercellular CO₂ when no measurable CO₂ fixation was sustained, an appreciable fraction of Q_A still remained oxidised, however, maximal reduction of Q_A occurred when O₂ was also removed. Q_A could then be substantially reoxidised by the readdition of small amounts of CO₂ (20-40 μmol) which only facilitated a very small increase in CO₂ fixation. Changes in the kinetics of the fast rise in fluorescence emission indicated that Q_A-to-Q_B electron transfer was decreased in a CO₂-free atmosphere and Q_B was poised in a more oxidised state. Electron transport that was independent of CO₂ fixation was measured in methyl viologen-treated leaf discs. In 1% O₂, but not in 21% O₂, light-dependent electron transport to methyl viologen was decreased significantly by the depletion of CO₂. It is concluded that CO₂ can modify the redox state of Photosystem II electron transport acceptors in vivo independently of carbon assimilation and that there is a complex interaction between CO₂ and O₂ in the regulation of photosynthetic electron transport. The possibility that CO₂ operates via the reversible binding to PS II and thereby acts as a cofactor for efficient PS II electron transport in the leaf is discussed.