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J. Biol. Chem., Vol. 261, Issue 26, 12172-12178, Sep, 1986
Calcium transport into the vacuole of oat roots. Characterization of H+/Ca2+ exchange activity
KS Schumaker and H Sze
Calcium (Ca2+) is sequestered into vacuoles of oat root cells through a
H+/Ca2+ antiport system that is driven by the proton-motive force of the
tonoplast H+-translocating ATPase. The antiport has been characterized
directly by imposing a pH gradient in tonoplast-enriched vesicles. The pH
gradient was imposed by diluting K+-loaded vesicles into a K+-free medium.
Nigericin induced a K+/H+ exchange resulting in a pH gradient of 2 (acid
inside). The pH gradient was capable of driving 45Ca2+ accumulation. Ca2+
uptake was tightly coupled to H+ loss as increasing Ca2+ levels
progressively dissipated the steady state pH gradient. Ca2+ uptake
displayed saturation kinetics with a Km(app) for Ca2+ of 10 microM. The
relative affinity of the antiporter for transport of divalent cations was
Ca2+ greater than Sr2+ greater than Ba2+ greater than Mg2+. La3+ or Mn2+
blocked Ca2+ uptake possibly by occupying the Ca2+-binding site. Ruthenium
red (I50 = 40 microM) and N,N'-dicyclohexylcarbodiimide (I50 = 3 microM)
specifically inhibited the H+/Ca2+ antiporter. When driven by pH jumps, the
H+/Ca2+ exchange generated a membrane potential, interior positive, as
shown by [14C]SCN accumulation. Furthermore, Ca2+ uptake was stimulated by
an imposed negative membrane potential. The results support a simple model
of one Ca2+ taken up per H+ lost. The exchange transport can be reversed,
as a Ca2+ gradient (Ca2+in greater than Ca2+out) was effective in forming a
pH gradient (acid inside). We suggest that the H+/Ca2+ exchange normally
transports Ca2+ into the vacuole; however, under certain conditions, Ca2+
may be released into the cytoplasm via this antiporter.

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Copyright © 1986 by the American Society for Biochemistry and Molecular Biology.
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