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  • Cell wall and calcium  (1)
  • Proton motive force  (1)
  • 1
    ISSN: 1432-2048
    Keywords: Chara ; Choride influx ; Cotransport ; pH jump ; Proton motive force
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Rapid lowering of the external pH (“pH jump”) enhances Cl− influx in Chara. Experiments were conducted to distinguish between two factors which have previously been proposed to mediate in the response: raised cytoplasmic pH and lowered cytoplasmic Cl− concentration. It is concluded that the latter alternative is more likely because: i) Cl− influx is reduced at high external pH; ii) influx following the pH jump is never greater than that following pretreatment in Cl−-free solution, which reduces cytoplasmic Cl− concentration (“Cl− starvation”); iii) the joint application of pH jump and Cl− starvation does not result in a greater Cl− influx than does Cl− starvation alone; and iv) addition of NH 4 + , which increases cytoplasmic pH, does generate an additional stimulation of Cl− influx following a pH jump. It is suggested that the increased cytoplasmic pH at the end of pretreatment at high external pH decays rapidly during the pH jump, and thus any effect on Cl− influx is so transient as to be undetectable by the methods used. The results are discussed in terms of a reaction kinetic model for 2H+/Cl− cotransport (Sanders, D. and Hansen, U.-P, 1981, J. Member. Biol. 58, 139–153) which describes quantitatively; i) the effects of NH 4 + on Cl− influx in terms involving only a change in cytoplasmic pH; and ii) the combined effects of Cl− starvation and NH 4 + in terms involving only changes in Cl− concentration and cytoplasmic pH. Conversely, the combined effects of Cl− starvation and pH jump cannot be described by the model if the effect of the pH jump is the consequence of increased cytoplasmic pH. The simple interpretation of experiments on whole cells involving manipulation of $$\Delta \bar \mu _{{\text{H}}^ + } $$ (the electrochemical potential difference for protons across the plasma membrane) is questioned in the light of these and previous findings that secondary factors can determine the response of Cl− transport in Chara.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Planta 186 (1992), S. 558-566 
    ISSN: 1432-2048
    Keywords: Calcium influx ; Cell wall and calcium ; Chara ; Cytoplasmic calcium concentration ; Lanthanum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract This paper deals with the effect of calcium binding in the cell wall on the measured 45Ca influx in Chara corallina Klein ex Will. esk. R.D. Wood. Calcium in the cell wall was in the range 687–1197 (μmol · m−2 compared to the sap which contained only 144–256 μmol · m−2. In dilute culture solutions the calcium content of the cell wall was relatively independent of external calcium at concentrations above about 0.1 mol · m−3. The half-times for exchange of calcium from 45Ca-labelled cell walls varied from 45 min at 0.05 mol · m−3 to less than 2 min at 2 mol · m−3. The effectiveness of other cations in displacing calcium from cell walls was in the order La 〉 Zn 〉 Co 〉 Ni 〉 Mg. Rinsing of 45Ca-labelled cell walls in 2 mol · m−3 LaCl3 for 20 min removed more than 99% of the bound 45Ca. However, the residual 45Ca activity in isolated cell walls following La3+ rinsing was similar to that in whole cells. It is concluded that in whole cells 45Ca influx cannot normally be distinguished from extracellular binding of calcium. Methods are described for the measurement of 45Ca fluxes in charophyte cells by isolation of intracellular 45Ca after the uptake period using techniques which avoid contamination from the large amount of tracer bound in the cell wall. At an external calcium concentration of 1 mol · m−3, the plasmalemma influx was approx. 0.2 nmol · m−2 · s−1 of which about half entered the vacuole and half was effluxed back into the external solution. The cytoplasm filled with calcium with a half-time of 40–50 min with an ‘apparent’ pool size of 50 mmol · m−3. After 2 h the net flux to the cell was almost the same as the vacuolar flux. The fluxes reported are an order of magnitude lower than previously reported calcium fluxes in plants.
    Type of Medium: Electronic Resource
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