scholarly journals Influx and accumulation of Cs+ by the akt1 mutant of Arabidopsis thaliana (L.) Heynh. lacking a dominant K+ transport system

2001 ◽  
Vol 52 (357) ◽  
pp. 839-844 ◽  
Author(s):  
Martin R. Broadley ◽  
Abraham J. Escobar‐Gutiérrez ◽  
Helen C. Bowen ◽  
Neil J. Willey ◽  
Philip J. White
2018 ◽  
Vol 9 ◽  
Author(s):  
Inas Al-Younis ◽  
Aloysius Wong ◽  
Fouad Lemtiri-Chlieh ◽  
Sandra Schmöckel ◽  
Mark Tester ◽  
...  

1977 ◽  
Vol 42 (2) ◽  
pp. 150-153 ◽  
Author(s):  
B. A. Horwitz ◽  
M. Eaton

The in vitro respiratory rates of liver and diaphragm from hamsters were compared before and after prolonged cold exposure (5 degrees C, 3–4 wk). In the presence or absence of glucose, respiratory rates were elevated in both tissues from the cold-acclimated hamsters, and these cold-induced increases were significantly reduced by ouabain. This ouabain inhibition is consistent with the hypothesis that cold exposure of these rodents stimulates the energy demands of the Na+/K+ transport system in liver and diaphragm, with these demands providing a driving force, at least in part, for respiration and accompanying cellular thermogenesis.


2000 ◽  
Vol 182 (2) ◽  
pp. 394-399 ◽  
Author(s):  
Fernando Calero ◽  
Néstor Gómez ◽  
Joaquín Ariño ◽  
José Ramos

ABSTRACT The trk1 + gene has been proposed as a component of the K+ influx system in the fission yeastSchizosaccharomyces pombe. Previous work from our laboratories revealed that trk1 mutants do not show significantly altered content or influx of K+, although they are more sensitive to Na+. Genome database searches revealed that S. pombe encodes a putative gene (designated here trk2 +) that shows significant identity totrk1 +. We have analyzed the characteristics of potassium influx in S. pombe by using trk1 trk2mutants. Unlike budding yeast, fission yeast displays a biphasic transport kinetics. trk2 mutants do not show altered K+ transport and exhibit only a slightly reduced Na+ tolerance. However, trk1 trk2 double mutants fail to grow at low K+ concentrations and show a dramatic decrease in Rb+ influx, as a result of loss of the high-affinity transport component. Furthermore, trk1 trk2cells are very sensitive to Na+, as would be expected for a strain showing defective potassium transport. When trk1 trk2 cells are maintained in K+-free medium, the potassium content remains higher than that of the wild type ortrk single mutants. In addition, the trk1 trk2strain displays increased sensitivity to hygromycin B. These results are consistent with a hyperpolarized state of the plasma membrane. An additional phenotype of cells lacking both Trk components is a failure to grow at acidic pH. In conclusion, the Trk1 and Trk2 proteins define the major K+ transport system in fission yeast, and in contrast to what is known for budding yeast, the presence of any of these two proteins is sufficient to allow growth at normal potassium levels.


1982 ◽  
Vol 242 (6) ◽  
pp. F690-F698
Author(s):  
O. A. Candia ◽  
P. S. Reinach

The formalism of linear nonequilibrium thermodynamics for a three-flow system was applied to the isolated frog corneal epithelium to study the coupling between metabolism and the Na-K transport system across this layer. There is little or no net ion transport across the isolated frog corneal epithelium bathed in Na2SO4 Ringer. Addition of amphotericin B to the tear side solution increases apical membrane permeability, which results in a net Na transport (from tear to stroma) and a net K transport in the opposite direction. Corneas were mounted in a modified Ussing chamber that permitted the simultaneous measurements of electrical parameters and O2 consumption by means of Clark-type oxygen electrodes. The overall degree of coupling, q, of the Na-K transport system to metabolism was calculated from measuring the suprabasal O2 consumption rate at "static head" and "level flow" conditions and by a second independent technique. Measurements of electrical conductance used in conjunction with other previously measured parameters allowed the calculation of the affinity, A, of the metabolic reaction driving transport, all phenomenological coefficients, and the electromotive forces of sodium (ENa) and potassium transport (EK). Values of q determined by the two techniques agreed (q = 0.80 and 0.84, respectively). This indicates incomplete coupling and a variable stoichiometric relationship among O2 consumption rate, net Na transport, and net K transport. The value calculated for A was 70.5 kcal.mol-1, for ENa 142.5 mV, and for EK -34.9 mV.


1992 ◽  
Vol 157 (2) ◽  
pp. 125-130 ◽  
Author(s):  
Paul Golby ◽  
Nicholas P. J. Cotton ◽  
Mark Carver ◽  
J. Baz Jackson

2019 ◽  
Vol 20 (5) ◽  
pp. 1085 ◽  
Author(s):  
Qian Wang ◽  
Chao Guan ◽  
Pei Wang ◽  
Qing Ma ◽  
Ai-Ke Bao ◽  
...  

HKT1 and SOS1 are two key Na+ transporters that modulate salt tolerance in plants. Although much is known about the respective functions of HKT1 and SOS1 under salt conditions, few studies have examined the effects of HKT1 and SOS1 mutations on the expression of other important Na+ and K+ transporter genes. This study investigated the physiological parameters and expression profiles of AtHKT1;1, AtSOS1, AtHAK5, AtAKT1, AtSKOR, AtNHX1, and AtAVP1 in wild-type (WT) and athkt1;1 and atsos1 mutants of Arabidopsis thaliana under 25 mM NaCl. We found that AtSOS1 mutation induced a significant decrease in transcripts of AtHKT1;1 (by 56–62% at 6–24 h), AtSKOR (by 36–78% at 6–24 h), and AtAKT1 (by 31–53% at 6–24 h) in the roots compared with WT. This led to an increase in Na+ accumulation in the roots, a decrease in K+ uptake and transportation, and finally resulted in suppression of plant growth. AtHKT1;1 loss induced a 39–76% (6–24 h) decrease and a 27–32% (6–24 h) increase in transcripts of AtSKOR and AtHAK5, respectively, in the roots compared with WT. At the same time, 25 mM NaCl decreased the net selective transport capacity for K+ over Na+ by 92% in the athkt1;1 roots compared with the WT roots. Consequently, Na+ was loaded into the xylem and delivered to the shoots, whereas K+ transport was restricted. The results indicate that AtHKT1;1 and AtSOS1 not only mediate Na+ transport but also control ion uptake and the spatial distribution of Na+ and K+ by cooperatively regulating the expression levels of relevant Na+ and K+ transporter genes, ultimately regulating plant growth under salt stress.


1994 ◽  
Vol 267 (4) ◽  
pp. C932-C939 ◽  
Author(s):  
E. Weil-Maslansky ◽  
Y. Gutman ◽  
S. Sasson

Insulin augments the activity of Na(+)-K(+)-adenosinetriphosphatase (ATPase) in skeletal muscles. This study shows that when furosemide- and bumetanide-inhibitable 86Rb+ uptake is measured in the skeletal muscle-like BC3H1 cell line, insulin and insulin-like growth factor I (IGF-I) activate a loop diuretic-sensitive K+ and Cl- transport system but have no effect on Na(+)-K(+)-ATPase. The insulin-stimulated K+ transport system is extracellular Na+ concentration ([Na+]o) independent and extracellular Cl- concentration ([Cl-]o) dependent. Na(+)-independent K(+)-Cl- cotransport systems have been identified in other cells, but their sensitivity to insulin or growth factors has not been described. The affinities of the insulin-stimulated K+ uptake in BC3H1 cells for K+ (0.9 +/- 0.1 mM) and loop diuretics (5.9 x 10(-7) and 10(-7) M for furosemide and bumetanide, respectively) are higher than those of K(+)-Cl- cotransporters in other cells. Thus the insulin-stimulated K+ and Cl- transport system in BC3H1 seems kinetically different from K(+)-Cl- cotransporters in other cells. Insulin and IGF-I may activate a unique K(+)-Cl- cotransporter or activate a [Na+]o-independent K(+)-Cl- cotransport mode of Na(+)-K(+)-Cl- cotransporter in BC3H1 cells.


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