Abstract
Plasma membrane vesicles, which are mostly right side-out, were isolated from corn leaves by aqueous two-phase partitioning method. Characteristics of Ca2+ transport were investigated after preparing inside-out vesicles by Triton X-100 treatment. 45Ca2+ transport was assayed by membrane filtration technique. Results showed that Ca2+ transport into the plasma membrane vesicles was Mg-ATP dependent. The active Ca2+ transport system had a high affinity for Ca2+(Km(Ca2+) = 0.4 microM) and ATP(Km(ATP) = 3.9 microM), and showed pH optimum at 7.5. ATP-dependent Ca2+ uptake in the plasma membrane vesicles was stimulated in the presence of Cl- or NO3-. Quenching of quinacrine fluorescence showed that these anions also induced H+ transport into the vesicles. The Ca2+ uptake stimulated by Cl- was dependent on the activity of H+ transport into the vesicles. However, carbonylcyanide m-chlorophenylhydrazone (CCCP) and VO4(3-) which is known to inhibit the H+ pump associated with the plasma membrane, canceled almost all of the Cl(-)-stimulated Ca2+ uptake. Furthermore, artificially imposed pH gradient (acid inside) caused Ca2+ uptake into the vesicles. These results suggest that the Cl(-)-stimulated Ca2+ uptake is caused by the efflux of H+ from the vesicles by the operation of Ca2+/H+ antiport system in the plasma membrane. In Cl(-)-free medium, H+ transport into the vesicles scarcely occurred and the addition of CCCP caused only a slight inhibition of the active Ca2+ uptake into the vesicles. These results suggest that two Ca2+ transport systems are operating in the plasma membrane from corn leaves, i.e., one is an ATP-dependent active Ca2+ transport system (Ca2+ pump) and the other is a Ca2+/H+ antiport system. Little difference in characteristics of Ca2+ transport was observed between the plasma membranes isolated from etiolated and green corn leaves.
MeSH Terms
Adenosine Triphosphate/physiology
Antiporters
Biological Transport, Active/drug effects
Calcium Channels/metabolism
Calcium-Binding Proteins/metabolism
Carbonyl Cyanide m-Chlorophenyl Hydrazone/pharmacology
Cation Transport Proteins
Cell Membrane/metabolism
Hydrogen-Ion Concentration
Lanthanum/pharmacology
Magnesium/physiology
Protons
Salts/pharmacology
Vanadates/pharmacology
Verapamil/pharmacology
Zea mays/metabolism
Chemicals
Antiporters
Calcium Channels
Calcium-Binding Proteins
Cation Transport Proteins
Protons
Salts
calcium-hydrogen antiporters
Vanadates
Carbonyl Cyanide m-Chlorophenyl Hydrazone
Lanthanum
Adenosine Triphosphate
Verapamil
Magnesium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Kasai M
Institute of Applied Microbiology, University of Tokyo, Japan.
Muto S
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