Phosphatase activities were measured in preparations of vacuoles isolated from storage roots of red beet (Beta vulgaris L.). The vacuoles possessed both acid phosphatase and ATPase activities which could be distinguished by their susceptibility to inhibition by low concentrations of ammonium molybda
Membrane-potential changes in vacuoles isolated from storage roots of red beet (Beta vulgarisL.)
โ Scribed by Anthony J. Miller; John J. Brimelow; Philip John
- Publisher
- Springer-Verlag
- Year
- 1984
- Tongue
- English
- Weight
- 733 KB
- Volume
- 160
- Category
- Article
- ISSN
- 0032-0935
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โฆ Synopsis
The membrane potential in vacuoles isolated from storage roots of red beet (Beta vulgaris L.) has been studied by following changes in the fluorescence of the dye 3,3'-diethylthiodicarbocyanine iodide, and by determining the uptake of the lipophilic triphenylmethylphosphonium cation.
The vacuoles have a membrane potential, internal negative, which is estimated to be around -60 inV. These potentials become less negative by nearly 10 mV on addition of ATP. This ATP-dependent depolarisation is inhibited by the protonophore carbonylcyanide p-trifluoromethoxyphenylhydrazone and by the ATPase inhibitors, N,N'dicyclohexylcarbodiimide and trimethyltin chloride, but it is largely insensitive to sodium orthovanadate. Fusicoccin had no significant effect on the isolated vacuoles, but its addition to excised tissue caused a hyperpolarisation of the cells measured using a microelectrode.
๐ SIMILAR VOLUMES
Vacuoles isolated from storage roots of red beet (Beta vulgaris L.) posess a Mg(2+)-dependent, alkaline pyrophosphatase (PPase) activity which is further stimulated by salts of monovalent cations. The requirement for Mg(2+) is specific. Mn(2+) and Zn(2+) permitted only 20% and 12%, respectively, of
Ion stimulation and some other properties of an ATPase activity associated with vacuoles isolated from storage roots of red beet (Beta vulgar& L.) have been determined. The ATPase had a specific requirement for Mg 2+ and in the presence of Mg 1+ it was stimulated by salts of monovalent cations. The