Skip to main content
The Journal of General Physiology logoLink to The Journal of General Physiology
. 1967 May 1;50(5):1303–1310. doi: 10.1085/jgp.50.5.1303

Binding of Ca Ions by Paramecium caudatum

Yutaka Naitoh 1, Ikuo Yasumasu 1
PMCID: PMC2225717  PMID: 6033587

Abstract

Binding of 45Ca by live Paramecium caudatum was determined under various external ionic conditions. It was found that calcium uptake was separable into at least two components, a rapid and a slow one. The rapid component was influenced by the presence of certain other ions in a manner which agrees with the law of mass action. It appears that an ion exchange system may be involved in a binding equilibrium established between Paramecium, Ca++, and certain other ions. K+, Rb+, and Ba++ in the equilibrium medium are among those ions which inhibit calcium uptake. It is proposed that liberation of Ca++ from binding sites on Paramecium by an exchange reaction with competing ions is the first step in the mechanism of ciliary reversal in the response to external application of these ions.

Full Text

The Full Text of this article is available as a PDF (492.1 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. CARVALHO A. P., SANUI H., PACE N. CALCIUM AND MAGNESIUM BINDING PROPERTIES OF CELL MEMBRANE MATERIALS. J Cell Physiol. 1963 Dec;62:311–317. doi: 10.1002/jcp.1030620311. [DOI] [PubMed] [Google Scholar]
  2. HUXLEY A. F. MUSCLE. Annu Rev Physiol. 1964;26:131–152. doi: 10.1146/annurev.ph.26.030164.001023. [DOI] [PubMed] [Google Scholar]
  3. JAHN T. L. The mechanism of ciliary movement. II. Ion antagonism and ciliary reversal. J Cell Comp Physiol. 1962 Dec;60:217–228. doi: 10.1002/jcp.1030600305. [DOI] [PubMed] [Google Scholar]
  4. KOKETSU K., KITAMURA R., TANAKA R. BINDING OF CALCIUM IONS TO CELL MEMBRANE ISOLATED FROM BULLFROG SKELETAL MUSCLE. Am J Physiol. 1964 Aug;207:509–512. doi: 10.1152/ajplegacy.1964.207.2.509. [DOI] [PubMed] [Google Scholar]
  5. MIKULECKY D. C., TOBIAS J. M. PHOSPHOLIPID-CHOLESTEROL MEMBRANE MODEL. I. CORRELATION OF RESISTANCE WITH ION CONTENT. II. CATION EXCHANGE PROPERTIES. 3. EFFECT OF CA ON SALT PERMEABILITY. IV. CA-K UPTAKE BY SONICALLY FRAGMENTED ERYTHROCYTE GHOSTS. J Cell Physiol. 1964 Oct;64:151–163. doi: 10.1002/jcp.1030640202. [DOI] [PubMed] [Google Scholar]
  6. Naitoh Y. Reversal response elicited in nonbeating cilia of paramecium by membrane depolarizatin. Science. 1966 Nov 4;154(3749):660–662. doi: 10.1126/science.154.3749.660. [DOI] [PubMed] [Google Scholar]
  7. SANUI H., CARVALHO A. P., PACE N. Relationship of hydrogen ion binding to sodium and potassium binding by rat liver cell microsomes and human erythrocyte ghosts. J Cell Comp Physiol. 1962 Jun;59:241–250. doi: 10.1002/jcp.1030590303. [DOI] [PubMed] [Google Scholar]
  8. TOBIAS J. M. A CHEMICALLY SPECIFIED MOLECULAR MECHANISM UNDERLYING EXCITATION IN NERVE: A HYPOTHESIS. Nature. 1964 Jul 4;203:13–17. doi: 10.1038/203013a0. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of General Physiology are provided here courtesy of The Rockefeller University Press

RESOURCES