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PMID: 24276764 Published · ppublish English Journal Article

Characterisation of a salt-stimulated ATPase activity associated with vacuoles isolated from storage roots of red beet (Beta vulgaris L.).

Planta ·Vol. 153 ·No. 2 ·1981-10-00 ·Pages 140-9

Walker RR, Leigh RA

Abstract

Ion stimulation and some other properties of an ATPase activity associated with vacuoles isolated from storage roots of red beet (Beta vulgaris L.) have been determined. The ATPase had a specific requirement for Mg(2+) and in the presence of Mg(2+) it was stimulated by salts of monovalent cations. The degree of stimulation by monovalent salts was influenced mainly by the anion and the order of effectiveness of the anions tested was Cl(-)>HCO 3 (-) >Br(-)>malate>acetate>SO 4 (2-) . For any given series of anions the magnitude of the stimulation obtained was influenced by the accompanying cation (NH 4 (+) ≫ Na(+)>K(+)). This cation effect was abolished by 0.01% (v/v) Triton X-100 and it is suggested that it is the result of different permeabilities of membrane vesicles to the cations. There was no evidence of synergistic stimulation of the ATPase by mixtures of Na(+) and K(+). KCl- and NaCl-stimulation was maximal with salt concentrations in the range 60-150 mM. The true substrate of the enzyme was shown to be MgATP. It was shown that KCl stimulation was the result of an increase in Vmax rather than a change in the affinity of the enzyme for MgATP. The ATPase was inhibited by N,N'-dicyclohexylcarbodiimide, diethylstilbestrol, mersalyl and KNO3 but other inhibitors tested (azide, oligomycin, orthovanadate, K3[Cr(oxalate)6] and ethyl-3-[3-dimethylaminopropyl]carbodiimide) were without effect or caused only partial inhibition at the highest concentration tested. The ATPase activity was equally distributed between pellet and supernatant fractions obtained after the subfractionation of vacuoles but the properties of the ATPase in each fraction were the same. It is suggested that beet vacuoles possess only one ATPase. The properties of the ATPase are compared with those of ATPases associated with other plant membranes and organelles and its possible role in transport at the tonoplast is discussed.

Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Walker R R
Botany School, University of Cambridge, Downing Street, CB2 3EA, Cambridge, UK.
Leigh R A
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Article Info
Journal
Planta
Abbr.
Planta
ISSN
0032-0935
Published
1981-10-00
Pages
140-9
Language
English
Region
Germany
NLM ID
1250576
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