ArticleThe Journal of membrane biology1994
Solute transport across the tonoplast of barely mesophyll vacuoles: Mg2+ determines the specificity, and ATP lipophilic amino acids the activity of the amino acid carrier.
Article in The Journal of membrane biology, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed, 8 citations in OpenAlex.
- ATP, pH and Mg2+ modulate a cation current in Beta vulgaris vacuoles: a possible shunt conductance for the vacuolar H(+)-ATPase.The Journal of membrane biology · 1995Article
- Dipeptide transport in barley mesophyll vacuoles.Planta · 1995Article
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
After stimulation with ATP and in the absence of divalent cations, isolated barely mesophyll vacuoles exhibited massive solute fluxes across the tonoplast, measured either as efflux of endogenous solutes or as uptake of radioactive-labeled compounds. Transported solutes were ions (particularly K+, NO3-, Cl-) and amino acids (for example, ala, arg, asp, gln, leu, met). Addition of Mg2+ in excess of added ATP inhibited fluxes of inorganic ions and of positively charged amino acids, but not, or to a smaller extent, those of neutral amino acids. Thus, Mg2+ increased the specificity of the carrier for amino acids such as alanine and glutamine. All ATP-stimulated transport processes were sensitive towards inhibition by lipophilic amino acids, for example by leucine and phenylalanine. After stimulation with sulfhydryl reagents, the inhibitory properties of Mg2+ and lipophilic amino acids were lost. These data concur with the hypothesis of a single transporter which exhibits a channel-like structure with a low degree of substrate selectivity in the absence of Mg2+, and which functions as a neutral amino acid carrier in the presence of Mg2+.
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