H+-ATPase Activity from Storage Tissue of Beta vulgaris
Authors:
- Sharman D. O'NeillSOSharman D. O'Neill
- Roger M. SpanswickRSRoger M. Spanswick
- 1 March 1984
- journal article
- research article
- Published by Oxford University Press (OUP) in Plant Physiology
- Vol. 74 (3) , 538-544
Abstract
Microsomal membranes isolated from red beet (Beta vulgaris L.) storage tissue were found to contain high levels of ionophore-stimulated ATPase activity. The distribution of this ATPase activity on a continuous sucrose gradient showed a low density peak (1.09 grams per cubic centimeter) that was stimulated over 400% by gramicidin and coincided with a peak of NO(3) (-)-sensitive ATPase activity. At higher densities (1.16-1.18 grams per cubic centimeter) a shoulder of gramicidin-stimulated ATPase that coincided with a peak of vanadate-sensitive ATPase was apparent. A discontinuous sucrose gradient of 16/26/34/40% sucrose (w/w) was effective in routinely separating the NO(3) (-)-sensitive ATPase (16/26% interface) from the vanadate-sensitive ATPase (34/40% interface). Both membrane fractions were shown to catalyze ATP-dependent H(+) transport, with the transport process showing the same differential sensitivity to NO(3) (-) and vanadate as the ATPase activity.Characterization of the lower density ATPase (16/26% interface) indicated that it was highly stimulated by gramicidin, inhibited by KNO(3), stimulated by anions (Cl(-) > Br(-) > acetate > HCO(3) (-) > SO(4) (2-)), and largely insensitive to monovalent cations. These characteristics are very similar to those reported for tonoplast ATPase activity and a tonoplast origin for the low density membrane vesicles was supported by comparison with isolated red beet vacuoles. The membranes isolated from the vacuole preparation were found to possess an ATPase with characteristics identical to those of the low density membrane vesicles, and were shown to have a peak density of 1.09 grams per cubic centimeter. Furthermore, following osmotic lysis the vacuolar membranes apparently resealed and ATP-dependent H(+) transport could be demonstrated in these vacuole-derived membrane vesicles. This report, thus, strongly supports a tonoplast origin for the low density, anion-sensitive H(+)-ATPase and further indicates the presence of a higher density, vanadate-sensitive, H(+)-ATPase in the red beet microsomal membrane fraction, which is presumably of plasma membrane origin.Keywords
This publication has 16 references indexed in Scilit:
- Characterization of a Proton-Translocating ATPase in Microsomal Vesicles from Corn RootsPlant Physiology, 1982
- Localization of the Proton Pump of Corn Coleoptile Microsomal Membranes by Density Gradient CentrifugationPlant Physiology, 1982
- Localization of a Proton-Translocating ATPase on Sucrose GradientsPlant Physiology, 1982
- Characterization of Nigericin-Stimulated ATPase from Sealed Microsomal Vesicles of Tobacco CallusPlant Physiology, 1982
- Evidence for a Cl−-Stimulated MgATPase Proton Pump in Oat Root MembranesPlant Physiology, 1982
- Enzymic and Protein Character of Tonoplast from Hippeastrum VacuolesPlant Physiology, 1981
- Evidence for an electrogenic ATPase in microsomal vesicles from pea internodesBiochimica et Biophysica Acta (BBA) - Biomembranes, 1981
- Isolation of Functionally Intact Rhodoplasts from Griffithsia monilis (Ceramiaceae, Rhodophyta)Plant Physiology, 1981
- Isolation of Tonoplast Vesicles from Tobacco ProtoplastsPlant Physiology, 1980
- Hydrolytic Enzymes in the Central Vacuole of Plant CellsPlant Physiology, 1979