MATERIALS AND METHODSPhotosynthetic carbon metabolism was characterized in four photoautotrophic cell suspension cultures. There was no apparent difference between two soybean (Glycine max) and one cotton (Gossypium hirsutum) cell line which required 5% CO2 for growth, and a unique cotton cell line that grows at ambient CO2 (660 microliters per liter). Photosynthetic characteristics in all four lines were more like C3 mesophyll leaf cells than the cell suspension cultures previously studied. The pattem of 14C-labeling reflected the high ratio of ribulosebisphosphate carboxylase to phosphoenolpyruvate carboxylase activity and showed that CO2 fixation occurred primarily by the C3 pathway. Photorespiration occurred at 330 microliters per liter CO2, 21% 02 as indicated by the synthesis of high levels of 14C-labeled glycine and seine in a pulse-chase experiment and by oxygen inhibition of CO2 fixation. Short-term CO2 fixation in the presence and absence of carbonic anhydrase showed C02, not HC03-, to be the main source of inorganic carbon taken up by the low C02-requiring cotton cells. The cells did not have a C02-concentrating mechanism as indicated by silicone oil centrifugation experiments. Carbonic anhydrase was absent in the low C02-requiring cotton cells, present in the high C02-requiring soybean cell lines, and absent in other high CO2 cell lines examined. Thus, the presence of carbonic anhydrase is not an essential requirement for photoautotrophy in cell suspension cultures which grow at either high or low CO2
Photoautotrophic Cell Suspension CulturesSoybean (Glycine max) cells and high C02-requiring cotton (Gossypium hirsutum) cells were grown at 5% C02 in a modified MS medium2 which contained thiamine and hormones as the only organic compounds (22). Cells were subcultured every 2 weeks. Low C02-requiring cotton cells were grown at ambient CO2, which was 660 ,L/L, in a modified MS medium (3,10), and were subcultured every 4 weeks. Cells were used in experiments 1 to 2 weeks after transfer, and were regularly found to be 90 to 95% viable as determined by phenosafranine staining (30). Prior to use, the cells were washed three times with the appropriate buffer (usually 30 mm Mops, pH 7.0). Cells stored for 4 h in buffer at 11 sE/m2 *s in a test tube or Petri dish showed less than a 10% decrease in the rate of '4C02-fixation.
CO2 FixationCells (10-20 ,ug