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  • Asparagus  (1)
  • Carbon dioxide  (1)
  • Springer  (2)
  • American Physical Society
  • 1
    ISSN: 1432-2048
    Keywords: ATPase ; Bicarbonate transport ; Carbon dioxide ; Carbonic anhydrase ; Eremosphaera ; Inor ganic carbon (dissolved)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Mass spectrometry was used to investigate the uptake of CO2 in Eremosphaera viridis DeBary. Upon illumination, cells preincubated at pH 7.5 with 100 μM dissolved inorganic carbon (DIC) rapidly depleted almost all the free CO2 from the medium. Rapid equilibrium between HCO 3 - and CO2 occurred upon addition of bovine carbonic anhydrase (CA) to the medium, showing that CO2 depletion resulted from a selective uptake of CO2 rather than an uptake of all inorganic carbon species. Glycolaldehyde (10 mM) completely inhibited CO2 fixation but had little effect on CO2 transport. Transfer of glycolaldehyde-treated cells to the dark caused a rapid efflux of CO2 from the unfixed intracellular DIC pool which was found to be at least threeto sixfold higher in concentration than that of the external medium. These results indicate that E. viridis actively transports CO2 against a concentration gradient. No external CA was detected in these cells either by potentiometric or mass-spectrometric assay. In the absence of external CA, the rate of photosynthetic O2 evolution in the pH range 7.5 to 8.0 did not exceed the calculated rate of CO2 supply, indicating a limited capacity for HCO2 uptake in these cells. Electrophysiological measurements indicate that CO2 uptake is electrically silent and thus is not a consequence of H+-CO2 symport activity. Microsomal membranes isolated from Eremosphaera showed ATPase activity which was enhanced by CO2. These results indicate that active CO2 uptake is mediated by an ATPase.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Planta 153 (1981), S. 210-216 
    ISSN: 1432-2048
    Keywords: Asparagus ; 5,5-Dimethyloxazolidine-2,4-dione ; Mesophyll ; Photosynthesis ; pH, intracellular
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The intracellular pH of isolated, photosynthetically active mesophyll cells of Asparagus sprengeri Regel has been determined, in the light and dark, by the distribution of the weak acid 5,5-dimethyl-[2-14C]oxazolidine-2,4-dione ([14C]DMO) between the cells and the liquid medium. [14C]DMO was taken up rapidly, reaching equilibrium in 7–10 min of incubation, but was not metabolized by the cells, and intracellular binding of the compound was minimal. The intracellular pH, measured at saturating light fluence and 1.5 mM sodium bicarbonate, was found to remain relatively constant at 6.95–7.21 over the external pH range of 5.5–7.2. Illumination of the cells increased the intracellular pH compared to dark controls. The pH of the cytoplasm, excluding and including the chloroplasts (“cytoplasmic” and “bulk cytoplasmic”, respectively) was calculated from the experimentally derived intracellular [14C]DMO concentration and estimates of the vacuolar, chloroplastic and cytoplasmic volumes. The calculated cytoplasmic pH was similar in the light and dark, being 7.75 and 7.74, respectively, while the calculated pH of bulk cytoplasm was 7.85 in the light and 7.49 in the dark. Theoretical analysis indicated that intracellular pH is a good indicator of changes in the bulk cytoplasmic pH but insensitive to changes in vacuolar pH. The external pH optimum for photosynthesis (O2 evolution) of isolated Asparagus cells was pH 7.2. At pH 8.0 photosynthesis was inhibited by 30% and at pH 5.25 by 45%. Inhibition at alkaline pH may be the result of a decrease in the pH gradient between the cells and the medium, causing CO2 limitation in the cell. At acid pH, decrease in internal pH caused by substantial accumulation of inorganic carbon may account for the loss in photosynthetic activity.
    Type of Medium: Electronic Resource
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