A. Laisk et A. Sumberg, PARTITIONING OF THE LEAF CO2 EXCHANGE INTO COMPONENTS USING CO2 EXCHANGE AND FLUORESCENCE MEASUREMENTS, Plant physiology, 106(2), 1994, pp. 689-695
Photorespiration was calculated from chlorophyll fluorescence and ribu
lose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) kinetics and com
pared with CO2 evolution rate in the light, measured by three gas-exch
ange methods in mature sunflower (Helianthus annuus L.) leaves. The ga
s-exchange methods were (a) postillumination CO2 burst at unchanged CO
2 concentration, (b) postillumination CO2 burst with simultaneous tran
sfer into CO2-free air, and (c) extrapolation of the CO2 uptake to zer
o CO2 concentration at Rubisco active sites. The steady-state CO2 comp
ensation point was proportional to O-2 concentration, revealing the Ru
bisco specificity coefficient (K-sp) of 86. Electron transport rate (E
TR) was calculated from fluorescence, and photorespiration rate was ca
lculated from ETR using CO2 and O-2 concentrations, K-sp, and diffusio
n resistances. The values of the best-fit mesophyll diffusion resistan
ce for CO2 ranged between 0.3 and 0.8 s cm(-1). Comparison of the gas-
exchange and fluorescence data showed that only ribulose-1,5-bisphosph
ate (RuBP) carboxylation and photorespiratory CO2 evolution were prese
nt at limiting CO2 concentrations. Carboxylation of a substrate other
than RuBP, in addition to RuBP carboxylation, was detected at high CO2
concentrations. A simultaneous decarboxylation process not related to
RuBP oxygenation was also detected at high CO2 concentrations in the
light. We propose that these processes reflect carboxylation of phosph
oenolpyruvate, formed from phosphoglyceric acid and the subsequent dec
arboxylation of malate.