Diffusion Limitations in Root Uptake of Cadmium and Zinc, But Not Nickel, and Resulting Bias in the Michaelis Constant

It has long been recognized that diffusive boundary layers affect the determination of active transport parameters, but this has been largely overlooked in plant physiological research. We studied the short-term uptake of cadmium (Cd), zinc (Zn), and nickel (Ni) by spinach (Spinacia oleracea) and tomato (Lycopersicon esculentum) in solutions with or without metal complexes. At same free ion concentration, the presence of complexes, which enhance the diffusion flux, increased the uptake of Cd and Zn, whereas Ni uptake was unaffected. Competition effects of protons on Cd and Zn uptake were observed only at a very large degree of buffering, while competition of magnesium ions on Ni uptake was observed even in unbuffered solutions. These results strongly suggest that uptake of Cd and Zn is limited by diffusion of the free ion to the roots, except at very high degree of solution buffering, whereas Ni uptake is generally internalization limited. All results could be well described by a model that combined a diffusion equation with a competitive Michaelis-Menten equation. Direct uptake of the complex was estimated to be a major contribution only at millimolar concentrations of the complex or at very large ratios of complex to free ion concentration. The true K_m for uptake of Cd²⁺ and Zn²⁺ was estimated at <5 nm, three orders of magnitude smaller than the K_m measured in unbuffered solutions. Published Michaelis constants for plant uptake of Cd and Zn likely strongly overestimate physiological ones and should not be interpreted as an indicator of transporter affinity.Internalization of metals by biota is traditionally described by Michaelis-Menten kinetics (Wilkinson and Buffle, 2004). The K_m corresponds to the concentration in solution at which the uptake is one-half of the maximal uptake, F_max. The Michaelis-Menten equation relates the uptake flux, F, to the free ion concentration at the site of uptake, [M]_s:If diffusion of a metal across a diffusive boundary layer adjacent to the roots is the rate-limiting step for uptake, the concentration at the site of uptake will be lower than that in the bulk solution. As a result, diffusion limitations result in an overestimate of the K_m, if the concentration at the root surface is assumed to be the same as in the bulk solution, as is usually done. This bias in K_m has been discussed in detail by Winne (1973) and has, for instance, been demonstrated experimentally for uptake of Glc in rabbit jejunum (Thomson and Dietschy, 1980) and for uptake of several sugars, amino acids, and bile acids in rat ileum (Wilson and Dietschy, 1974).Models used to predict ion availability and toxicity of metals by plants usually rely on the assumption that uptake is controlled by the free metal ion activity and the activity of competing ions in the bulk solution. For instance, the biotic ligand model (BLM), originally developed to predict metal toxicity to aquatic organisms, assumes that toxicity of an ion is mitigated by the presence of competing ions that bind on the biotic ligand (Paquin et al., 2002). Hough et al. (2005) used a free ion activity model taking into account proton competition effects to predict cadmium (Cd) uptake by soil-grown ryegrass (Lolium perenne). The uptake was reasonably well predicted; however, as the authors pointed out, it was not clear whether the derived constants truly represented physiological affinity constants or were just fitting parameters in a rate-limited uptake process. In case of strong diffusion limitation, ion competition effects on the internalization are expected to have negligible effect on the uptake, as the uptake is controlled by diffusion and not by internalization (Campbell et al., 2002; Degryse and Smolders, 2012).In previous studies, we found strong evidence that uptake of Cd and zinc (Zn) is limited by the diffusive transport of the free metal ion to the root at low free ion concentration. At constant free ion concentration, the uptake of Cd and Zn increased in presence of metal complexes and the contribution of the complex increased with increasing dissociation rate of the complex (Degryse et al., 2006a, 2006c). In unbuffered solutions, i.e. solutions without metal complexes, stirring increased Cd uptake by plants (Degryse and Smolders, 2012). For nickel (Ni), however, contribution of complexes was small or undetectable, and stirring did not increase the uptake (Degryse and Smolders, 2012). Given this evidence that Cd and Zn uptake by plants is limited by diffusion, it is likely that published K_m values for uptake of Cd²⁺ and Zn²⁺ by plants overestimate true physiological values. This bias in the K_m when a diffusive boundary layer is present has been largely ignored in plant-physiological research. Indeed, in numerous studies the K_m value has been interpreted as a characteristic of the carrier-mediated transport process, while in many cases it may reflect mass transfer properties. In addition, these diffusion limitations may mask ion competition effects in the uptake.The aim of this article was (1) to present evidence that K_m values determined for Cd²⁺ and Zn²⁺ uptake by plants in general reflect transport limitations rather than transporter affinity; (2) to derive true K_m values by determining the K_m under conditions where the uptake is not transport limited; (3) to identify the consequence of diffusion limitations on competition effects; and (4) to describe uptake of Cd, Zn, and Ni by plants in a single comprehensive model that combines competitive Michaelis-Menten kinetics with a diffusion equation.

Theoretical Framework

In the following, we qualitatively discuss the bias in the K_m because of diffusion limitations, based on Figure 1. Equations are given in the “Materials and Methods” section. Figure 1A presents a case where the potential internalization flux by the plant at low concentrations is much larger than the maximal rate at which the free ion can be supplied through diffusive transport of the ion to the root surface. In this case, the actual uptake flux by the plant will approach the maximal diffusive flux, and the free ion concentration at the root surface is much smaller than that in the bulk solution. The apparent K_m (K_m*; determined as the concentration where the uptake flux is one-half of the maximal uptake) is much larger than the true K_m value. In Figure 1B, the potential internalization flux at low concentration is of the same order of magnitude as the maximal diffusion flux. In this case, the concentration at the root surface is slightly smaller than that in the bulk solution, and there is only a slight bias in the K_m value.Open in a separate windowFigure 1.Conceptual diagram of the internalization flux (Michaelis-Menten curve; full line), maximal diffusive supply from solution to root (dashed line), and actual uptake flux (dotted line) as a function of free ion concentration for two theoretical cases. Left and right sections show the same curves, on log (left) or linear (right) scale. In A, the potential internalization flux is much larger than the maximal diffusive supply at low concentrations, i.e. the uptake is strongly limited by the transport of the free ion to the root. The plant acts as a near-zero sink, and the actual plant uptake equals the maximal diffusive flux. The K_m* is much larger than the true K_m, and the experimental permeability P (slope of the actual uptake curve) is much smaller than the membrane permeability P_m (slope of the internalization curve). In B, the maximal diffusive flux is larger than the potential internalization flux. The uptake is not limited by diffusive transport, and the K_m* and true K_m are almost equal.Given the evidence that uptake of Cd and Zn by plants is diffusion limited, even in stirred nutrient solutions, we hypothesize that reported K_m values of Cd²⁺ and Zn²⁺ are biased, and that the physiological K_m values are much smaller. To test this hypothesis, we measured the uptake of Cd, Zn, and Ni in solution, in absence or in presence of labile hydrophilic metal complexes. If diffusion limitations prevail, the complexes dissociate within the diffusion layer and thus enhance the diffusion flux and therefore the metal uptake. By adding labile complexes in large amounts, it should be possible to abolish the diffusion barrier completely, in which case the physiological K_m can be determined.In addition, the effect of competitive ions on uptake was tested. The presence of competitive ions decreases the internalization flux. However, if uptake is rate limited by the diffusive transport to the uptake site and not by internalization, competition effects should theoretically not affect the uptake flux.     

Regulation of auxin transport in pea (Pisum sativum L.) by phenylacetic acid: effects on the components of transmembrane transport of indol-3yl-acetic acid

Phenylacetic acid (PAA), a naturally-occurring acidic plant growth substance, was readily taken up by pea (Pisum sativum L. cv. Alderman) stem segments from buffered external solutions by a pH-dependent, non-mediated diffusion. Net uptake from a 0.2 M solution at pH 4.5 proceeded at a constant rate for at least 60 min and, up to approx. 100 M, the rate of uptake was directly proportional to the external concentration of the compound. The net rate of uptake of PAA was not affected by the inclusion of indol-3yl-acetic acid (IAA) in the uptake medium (up to approx. 30 M) and, unlike the net uptake of IAA, was not stimulated by N-1-naphthylphthalamic acid (NPA) or 2,3,5-triiodobenzoic acid. At an external concentration of 0.2 M and pH 4.5, the net rate of uptake of PAA was about twice that of IAA. It was concluded that the uptake of PAA did not involve the participation of carriers and that PAA was not a transported substrate for the carriers involved in the uptake and polar transport of IAA. Nevertheless, the inclusion of 3–100 M unlabelled PAA in the external medium greatly stimulated the uptake by pea stem segments of [1-¹⁴C]IAA (external concentration 0.2 M). It was concluded that whilst PAA was not a transported substrate for the NPA-sensitive IAA efflux carrier, it interacted with this carrier to inhibit IAA efflux from cells. Over the concentration range 3–100 M, PAA progressively reduced the stimulatory effect of NPA on IAA uptake, indicating that PAA also inhibited carrier-mediated uptake of IAA. The consequences of these observations for the regulation of polar auxin transport are discussed.Abbreviations IAA indol-3yl-acetic acid - DMO 5,5-dimethyloxazolidine-2,4-dione - NPA N-1-naphthylphthalamic acid - PAA phenylacetic acid - TIBA 2,3,5-triiodobenzoic acid     

Sulphate uptake and metabolism in the chrysomonad,Monochrysis lutheri

The intracellular concentration of inorganic ³⁵SO₄ in Monochrysis lutheri cells exposed to 0.513 mM Na₂ ³⁵SO₄ for up to 6-hr remained constant at about 0.038 mM. The exchange rate of this ³⁵SO₄ with the external unlabelled sulphate was negligible compared to the rate of influx across the plasmalemma (0.032 μmoles/g cells/hr). The flux of free ³⁵SO₄ to organic ³⁵S was 0.029 μmoles/g cells/hr. Assuming an internal electrical potential in the cells of-70 mV, this intracellular concentration of inorganic ³⁵SO₄ was well in excess of that obtainable by passive diffusion as calculated from the Nernst equation. These results indicate that sulphate is accumulated by an active mechanism rather than by facilitated diffusion. Sulphate uptake appears to occur via a carrier-mediated membrane transport system which conforms to Michaelis-Menten type saturation kinetics with a K _m of 3.2×10^-5 M and a V _max of 7.9×10^-5 μmoles sulphate/hr/10⁵ cells. Uptake was dependent on a source of energy since the metabolic inhibitor CCCP almost completely inhibited uptake under both light and dark conditions and DCMU caused a 50% decrease in uptake under light conditions. Under dark conditions, uptake remained at about 80% of that observed under light conditions and was little affected by DCMU, indicating that the energy for uptake could be supplied by either photosynthesis or respiration. A charge and size recognition site in the cell is implied by the finding that sulphate uptake was inhibited by chromate and selenate but not by tungstate, molybdate, nitrate or phosphate. Chromate did not inhibit photosynthesis. Cysteine and methionine added to the culture medium were apparently capable of exerting inhibition of sulphate uptake in both unstarved and sulphate-starved cells. Cycloheximide slightly inhibited sulphate uptake over an 8-hr period indicating, either a slow rate of entry of the inhibitor into the cells or a slow turnover of the proteins(s) associated with sulphate transport.     

2,3-Dimercaptopropanol Inhibits Ca2+ Transport in Microsomes from Brain But Not from Fast-Skeletal Muscle

Ca²⁺ is involved in the regulation of a variety of physiological processes, but a persistent increase in free cytosolic Ca²⁺ concentrations may contribute to cell injury. Dimercaprol (BAL) is a compound used in the treatment of mercury intoxication, but presents low therapeutic efficacy. The molecular mechanism responsible for the BAL toxicity is poorly known. In the present study, the effect of BAL and inorganic and organic mercury on Ca²⁺ transport by Ca²⁺-ATPases located in the sarco/endoplasmic reticulum of fast-skeletal muscle and brain was examined. Ca²⁺ uptake by brain and fast-skeletal muscle microsomes was inhibited in a dose-dependent manner by Hg²⁺. The calculated IC₅₀ for Ca²⁺ uptake inhibition by HgCl₂ was 1.05 ± 0.09 M (n = 8) for brain and 0.72 ± 0.06 M (n = 9) for muscle. The difference was significant at p < 0.01 (data expressed as mean ± SD). At a low concentration (1 M), 2,3-dimercaptopropanol had no effect on Ca²⁺ uptake by brain or muscle vesicles and did not abolish the inhibition caused by Hg²⁺. A high concentration of BAL (1 mM) nearly abolished the inhibition caused by 1.75 M HgCl₂ or 6 M CH₃HgCl in skeletal muscle. Surprisingly, at intermediate concentrations (40–100 M) BAL partially inhibited Ca²⁺ transport in brain but had no effect on muscle. Furthermore, ATP hydrolysis by brain or muscle microsomes was not inhibited by BAL. These results suggest that in brain microsomes BAL affects in a different way Ca²⁺ transport and ATP hydrolysis. The increase in BAL concentration observed after toxic administration of this compound to experimental animals may contribute to deregulate Ca²⁺ homoeostasis and, consequently, to the neurotoxicity of BAL.     

Taenia crassiceps: absorption of hexoses and partial characterization of Na + -dependent glucose absorption by larvae

The uptake of ¹⁴C-fructose by T. crassiceps larvae was linear with respect to concentration. Uptake of 0.05 mM¹⁴C-fructose was not inhibited by 5.0 mM unlabeled fructose, tagatose, or sorbose. Fructose appears to enter larvae by diffusion only. The uptake of radioglucose and radiogalactose was not linear with respect to concentration at low substrate concentrations; at high substrate concentrations, the uptake of both hexoses was linear with respect to concentration. Inhibitor studies indicated that both glucose and galactose enter larvae by a combination of diffusion and a mediated process, and that these hexoses are mutually competitive inhibitors of one another. The uptake of glucose and galactose was also inhibited by α-and β-methyl glucoside, fucose, and phlorizin, but not by several amino acids, certain sugar analogs, nor ouabain. Glucose transport is Na⁺ sensitive; K⁺ was demonstrated to be a competitive inhibitor of Na⁺ activation of glucose uptake. After a 90-min incubation in 5 mM unlabeled glucose, larvae accumulated glucose against an apparent concentration difference. Although larvae appear freely permeable to ouabain, this compound had no apparent effect on glucose accumulation. The results of this study are compared with previous studies on Hymenolepis diminuta, Calliobothrium verticillatum, Hydatigera (Taenia) taeniaeformis, and mammalian systems.     

Chromium uptake and transport in barley seedlings (Hordeum vulgare L.)

Summary Potassium chromate is more toxic to the growth of barley in solution culture than chromic chloride, though apparent uptake of the latter is much faster. Inhibitor studies indicate that CrO₄ ^2- uptake is active whereas Cr³⁺ uptake is passive, demonstrating that the two forms do not share a common uptake mechanism. Studies on the form of Cr inside root cells show that in plants fed CrO₄ ^2- the Cr remains largely unchanged whereas in plants fed Cr³⁺ a little CrO₄ ^2- (0.5 per cent) is produced. This conversion is dependent on the presence of living material and is probably enzymatic. Chromate uptake follows Michaelis-Menten kinetics at low concentration and is competitively inhibited by sulphate. Transport of chromium up the root is very slow, accounting for the low levels of Cr in the shoots. Chromate is transported better than Cr³⁺ though still to a very limited extent. These experiments provide a physiological basis for previous observations.     

Potassium/proton exchange in brush-border membrane of rat ileum

Summary These experiments were designed to determine whether proton-driven⁸⁶Rb uptake was present in apical membrane vesicles prepared from rat ileum. The uptake of⁸⁶Rb was approximately 300 to 350% greater in the presence of a 100-fold H⁺ gradient than in its absence and was greater at 1, 2 and 5 minutes (overshoot) than that at 90 minutes. Proton-driven⁸⁶Rb uptake was decreased by 20% in TMA-nitrate compared to that in TMA-gluconate. 0.3mm amiloride did not significantly inhibit proton-driven⁸⁶Rb uptake; in contrast, proton-driven²²Na uptake was significantly inhibited by 0.3mm amiloride by 34%. Similarly, 25mm KCl inhibited proton-driven⁸⁶Rb uptake more than that of²²Na, while the inhibition of proton-driven²²Na uptake by 25mm NaCl was greater than that of⁸⁶Rb. In additional studies intravesicular acidification measured by acridine orange fluorescence was demonstrated in the presence of an out-wardly directed K gradient. These studies demonstrate that a proton gradient stimulates⁸⁶Rb uptake and a K gradient induces intravesicular acidification; and that these fluxes are mediated by a K/H exchange distinct from Na/H exchange which is also present in this membrane. We conclude that a specific exchange process for K/H is located in ileal apical membrane vesicles.     

Sodium dependency of GABA uptake into glial cells in bullfrog sympathetic ganglia

The kinetics of sodium dependency of GABA uptake by satellite glial cells was studied in bullfrog sympathetic ganglia. GABA uptake followed simple Michaelis-Menten kinetics at all sodium concentrations tested. Increasing external sodium concentration increased bothK _m andV _max for GABA uptake, with an increase in theV _max/K _m ratio. The initial rate of uptake as a function of the sodium concentration exhibited sigmoid shape at 100 M GABA. Hill number was estimated to be 2.0. Removal of external potassium ion or 10 M ouabain reduced GABA uptake time-dependently. The effect of ouabain was potentiated by 100 M veratrine. These results suggest that at least two sodium ions are involved with the transport of one GABA molecule and that sodium concentration gradient across the plasma membrane is the main driving force for the transport of GABA. The essential sodium gradient may be maintained by Na⁺, K⁺-ATPase acting as an ion pump.     

Electrogenic calcium transport in plasma membrane of rat pancreatic acinar cells

Summary ATP-dependent⁴⁵Ca²⁺ uptake was investigated in purified plasma membranes from rat pancreatic acinar cells. Plasma membranes were purified by four subsequent precipitations with MgCl₂ and characterized by marker enzyme distribution. When compared to the total homogenate, typical marker enzymes for the plasma membrane, (Na⁺,K⁺)-ATPase, basal adenylate cyclase and CCK-OP-stimulated adenylate cyclase were enriched by 43-fold, 44-fold, and 45-fold, respectively. The marker for the rough endoplasmic reticulum was decreased by fourfold compared to the total homogenate. Comparing plasma membranes with rough endoplasmic reticulum, Ca²⁺ uptake was maximal with 10 and 2 mol/liter free Ca²⁺, and half-maximal with 0.9 and 0.5 mol/liter free Ca²⁺. It was maximal at 3 and 0.2 mmol/liter free Mg²⁺ concentration, at an ATP concentration of 5 and 1 mmol/liter, respectively, and at pH 7 for both preparations. When Mg²⁺ was replaced by Mn²⁺ or Zn²⁺ ATP-dependent Ca²⁺ uptake was 63 and 11%, respectively, in plasma membranes; in rough endoplasmic reticulum only Mn²⁺ could replace Mg²⁺ for Ca²⁺ uptake by 20%. Other divalent cations such as Ba²⁺ and Sr²⁺ could not replace Mg²⁺ in Ca²⁺ uptake. Ca²⁺ uptake into plasma membranes was not enhanced by oxalate in contrast to Ca²⁺ uptake in rough endoplasmic reticulum which was stimulated by 7.3-fold. Both plasma membranes and rough endoplasmic reticulum showed cation and anion dependencies of Ca²⁺ uptake. The sequence was K⁺>Rb⁺>Na⁺>Li⁺>choline⁺ in plasma membranes and Rb⁺K⁺Na⁺>Li⁺>choline⁺ for rough endoplasmic reticulum. The anion sequence was Cl^–Br^–I^–>SCN^–>NO ₃ ^– >isethionate^– >cyclamate^–>gluconate^–>SO ₄ ^2– glutarate^– and Cl^–>Br>gluconate>SO ₄ ^2– >NO ₃ ^– >I^–>cyclamate^–SCN^–, respectively. Ca²⁺ uptake into plasma membranes appeared to be electrogenic since it was stimulated by an inside-negative K⁺ and SCN diffusion potential and inhibited by an inside-positive diffusion potential. Ca²⁺ uptake into rough endoplasmic reticulum was not affected by diffusion potentials. We assume that the Ca²⁺ transport mechanism in plasma membranes as characterized in this study represents the extrusion system for Ca²⁺ from the cell that might be involved in the regulation of the cytosolic Ca²⁺ level.     

Na+/Ca2+ countertransport in plasma membrane of rat pancreatic acinar cells

Summary The presence of a coupled Na⁺/Ca²⁺ exchange system has been demonstrated in plasma membrane vesicles from rat pancreatic acinar cells. Na⁺/Ca²⁺ exchange was investigated by measuring⁴⁵Ca²⁺ uptake and⁴⁵Ca²⁺ efflux in the presence of sodium gradients and at different electrical potential differences across the membrane (=) in the presence of sodium. Plasma membranes were prepared by a MgCl₂ precipitation method and characterized by marker enzyme distribution. When compared to the total homogenate, the typical marker for the plasma membrane, (Na⁺+K⁺)-ATPase was enriched by 23-fold. Markers for the endoplasmic reticulum, such as RNA and NADPH cytochromec reductase, as well as for mitochondria, the cytochromec oxidase, were reduced by twofold, threefold and 10-fold, respectively. For the Na⁺/Ca²⁺ countertransport system, the Ca²⁺ uptake after 1 min of incubation was half-maximal at 0.62 mol/liter Ca²⁺ and at 20 mmol/liter Na⁺ concentration and maximal at 10 mol/liter Ca²⁺ and 150 mmol/liter Na⁺ concentration, respecitively. When Na⁺ was replaced by Li⁺, maximal Ca²⁺ uptake was 75% as compared to that in the presence of Na⁺. Amiloride (10^–3 mol/liter) at 200 mmol/liter Na⁺ did not inhibit Na⁺/Ca²⁺ countertransport, whereas at low Na⁺ concentration (25 mmol/liter) amiloride exhibited dose-dependent inhibition to be 62% at 10^–2 mol/liter. CFCCP (10^–5 mol/liter) did not influence Na⁺/Ca²⁺ countertransport. Monensin inhibited dose dependently; at a concentration of 5×10^–6 mol/liter inhibition was 80%. A SCN^– or K⁺ diffusion potential (=), being positive at the vesicle inside, stimulated calcium uptake in the presence of sodium suggesting that Na⁺/Ca²⁺ countertransport operates electrogenically, i.e. with a stoichiometry higher than 2 Na⁺ for 1 Ca²⁺. In the absence of Na⁺, did not promote Ca²⁺ uptake. We conclude that in addition to ATP-dependent Ca²⁺ outward transport as characterized previously (E. Bayerdörffer, L. Eckhardt, W. Haase & 1. Schulz, 1985,J. Membrane Biol. 84:45–60) the Na⁺/Ca²⁺ countertransport system, as characterized in this study, represents a second transport system for the extrusion of calcium from the cell. Furthermore, the high affinity for calcium suggests that this system might participate in the regulation of the cytosolic free Ca²⁺ level.     

A choline transporter in renal brush-border membrane vesicles: Energetics and structural specificity

Summary Choline is a quaternary ammonium compound that is normally reabsorbed by the renal proximal tubule, despite its acknowledged role as a substrate for the renal organic cation (OC) secretory pathway. The basis for choline reabsorption was examined in studies of transport in rabbit renal brush-border membrane vesicles (BBMV). Although an outwardly directed H⁺ gradient (pH 6.0_in 7.5_out) stimulated uptake of tetraethylammonium (TEA), a model substrate of the OC/H⁺ exchanger in renal BBMV, it had no effect on uptake of 1 m choline. A 5 mm trans concentration gradient of choline did, however, drive countertransport of both TEA and choline, although trans TEA had no effect on choline accumulation in BBMV. A 20 mm concentration of unlabeled choline blocked uptake of both choline and TEA by >85%, whereas 20 mm TEA blocked only TEA uptake. The kinetics of choline uptake into vesicles preloaded with 1 mm unlabeled choline appeared to involve two, saturable transport processes, one of high affinity for choline (K _t of 97 m) and a second of low affinity (K _t of 10 mm), the latter presumably reflecting a weak interaction of choline with the OC/H⁺ exchanger. An inside-negative electrical PD stimulated the rate of uptake and supported the transient concentrative accumulation of choline in BBMV. The high affinity transporter showed a marked specificity for choline and closely related analogues. A model of the molecular determinants of substrate-transporter interaction is described. We conclude that the electrogenic high affinity pathway plays a central role in renal reabsorption of choline.We thank Dr. William Dantzler for helpful discussions. This work was supported by grants from the National Institutes of Health (PO1 DK41006) and the Arizona Disease Control Research Commission (82-0701).     

Carbon-dioxide exchange in lichens: determination of transport and carboxylation characteristics

Measurements were made of net rates of CO₂ assimilation in lichens at various ambient concentrations of CO₂ in air and in helox (79% He, 21% O₂). Because of the faster rate of CO₂ diffusion in the pores of lichen thalli when filled with helox than when filled with air, a given net rate of assimilation was achieved at a lower ambient concentration of CO₂ in helox. The differences were used to estimate resistances to diffusion through the gas-filled pore systems in lichens. The technique was first tested with five lichen species, and then applied in a detailed study with Ramalina maciformis, in which gas-phase resistances were determined in samples at four different states of hydration and with two irradiances. By assuming, on the basis of previous evidence, that the phycobiont in R. maciformis is fully turgid and photosynthetically competent at the smallest hydration imposed (equilibration with vapour at 97% relative humidity), and that, with this state of hydration, diffusion of CO₂ to the phycobiont takes place through continuously gas-filled pores, it was possible also to determine both the dependence of net rate of assimilation in the phycobiont on local concentration of CO₂ in the algal layer, and, with the wetter samples, the extents to which diffusion of CO₂ to the phycobiont was impeded by water films. In equilibrium with air of 97% relative humidity, the thallus water content being 0.5 g per g dry weight, the resistance to CO₂ diffusion through the thallus was about twice as large as the resistance to CO₂ uptake within the phycobiont. Total resistance to diffusion increased rapidly with increase in hydration. At a water content of 2 g per g it was about 50 times as great as the resistance to uptake within the phycobiont and more than two-thirds of it was attributable to impedance of transfer by water. The influences of water content on rate of assimilation at various irradiances are discussed. The analysis shows that the local CO₂ compensation concentration of the phycobiont in R. maciformis is close to zero, indicating that photorespiratory release of CO₂ does not take place in the alga, Trebouxia sp., under the conditions of these experiments.Symbols and Units rate of CO₂ diffusion in air relative to that in carrier gas (unity if the carrier gas is air and 0.43 if is helox) - A₁ net rate of CO₂ uptake by the lichen - A_p gross rate of carboxylation minus photorespiratory decarboxylation in the phycobiont, i.e. net rate of light-activated CO₂ exchange - A_* maximum, CO₂-saturated magnitude of A_p - c concentration of CO₂ - c_a ambient concentration of CO₂ - c_i c_a minus difference in CO₂ concentration across air-filled pore space in the thallus - c₈ CO₂ concentration equivalent to partial pressure of CO₂ at the surface of the phycobiont - ₁ magnitude of c_a at which A₁ = 0 - _* magnitude of c_* at which A_p = 0 - R rate of dark respiration in the lichen (mycobiont and phycobiont) - R rate of dark respiration in region between the surface of the lichen and an arbitrary distance from the surface within the thallus - r resistance to CO₂ transfer from lichen surface to the surface of the phycobiont - r resistance to CO₂ transfer between effective source of dark respiration in the lichen and the surface of the phycobiont - r_g, r _g components of r and r, respectively, attributable to transfer in air-phase - r_w, r _w components of r and r, respectively, attributable to transfer in water-phase - r component of r between surface of lichen and an arbitrary distance from the surface within the thallus - r_* resistance to CO₂ transfer and carboxylation in the phycobiont - RH relative humidity     

Salinity dependence,uptake kinetics,and specificity of amino-acid absorption across the body surface of the oligochaete annelidEnchytraeus albidus

Enchytraeus albidus is able to absorb dissolved¹⁴C-labeled neutral amino acids (glycine, L-alanine, L-valine,-aminoisobutyric acid) and an amino-acid mixture from ambient water across the body surface against considerable concentration gradients. Saturation kinetics and susceptibility of glycine uptake to competitive inhibition by alanine suggest mediated transport. Absorption of neutral amino acids is an active process. Exchange diffusion of preloaded-aminoisobutyric acid against external glycine or-aminoisobutyric acid could not be detected. Results on inhibition of glycine uptake by a variety of low-molecular-weight substances indicate that glycine absorption is highly specific for neutral amino acids and somewhat less for basic amino acids; it is unspecific for non--amino acids, acidic amino acids, carbohydrates, and organic acids. Rates of transintegumentary net influx of glycine are nearly identical to¹⁴C-glycine influx, suggesting that only small amounts of amino acids are released, as compared with the capacity for uptake. Thus,¹⁴C-amino-acid influx data are used for characterization of the uptake system. Glycine uptake is positively correlated to external salinity. In fresh water, absorption is nearly zero; between 10 and 20 S, uptake increases markedly reaching maximum values at 30 S; these remain almost constant at 40 S. Transport constants and maximum uptake rates increase with rising salinities. Since absorption of glycine and L-valine is susceptible to sodium depletion, similar mechanisms presumably underly salinity-dependent uptake of amino acids and sodium-dependent solute transport. Oxygen consumption is not significantly modified by different external salinities. Estimates of nutritional profit gained from absorption of amino acids vary between 4 and 15 % of metabolic rate for glycine absorption and between 10 and 39 % for uptake of an amino-acid mixture, according to external concentrations (10 and 50 µM) and salinities (20 and 30 S).     

Temporal and local concentration changes in diffusion layers at cellulose membranes due to concentration differences between the solutions on both sides of the membrane

Summary By means of a laser-interferometrical method diffusion layers at the interface of a noncharged cellulose membrane are studied. These layers are induced by a concentration difference between the NaCl solutions separated by the membrane. The temporal and local shift of the NaCl concentration in the diffusion layers were measured. A steady-state concentration profile could be obtained for times of 121 sect ₀484 sec. The concentration profiles at any time (t ₀900) are not a linear function of the membrane surface, but could be fitted to a quadratic function. The thickness of the diffusion layers is also a function of time and its stationary value in this system is (575±49)×10^–6 m. The role of concentration polarization for the determination of phenomenological thermodynamic coefficients of membranes is discussed and a new method is suggested, which excludes the difficulties of the concentration polarization in the diffusion layers at the membrane.     

Uptake of Some Quaternary Ammonium Ions by Human Erythrocytes

In many biophysical studies on erythrocytes some quaternary ammonium ions are used as replacements for Na⁺ and K⁺ of the physiological solutions. The object of this work was to study the possible uptake of quaternary ammonium ions by erythrocytes. Uptake of C¹⁴–choline chloride and C¹⁴–tetramethylammonium chloride by human erythrocytes was proved. It was shown that the compounds were neither incorporated into phospholipids of the cell nor converted to any other metabolites. Studies of uptake as a function of time, at several external concentrations of choline and tetramethylammonium, showed that within the first 4 hours uptake was a linear function of time regardless of the external concentration of the quaternary ammonium ions. The effects of various external concentrations of choline and tetramethylammonium ions on the rate of uptake by the cells were studied. The results showed the presence of two distinct mechanisms for the uptake of choline: one, a facilitated uptake mechanism which becomes saturated at low external concentrations of the ion; the other, a simple diffusion mechanism in which the rate of uptake is proportional to concentration. For the facilitated part of the uptake the external choline concentration at which half-maximum rate was obtained was found to be 0.02 mm. Although the kinetic studies with tetramethylammonium ion were not as extensive as those with choline, they did suggest the presence of similar mechanisms for the uptake of both ions. Tetramethylammonium and tetraethylammonium ions were shown to be competitive inhibitors of the facilitated choline uptake.     

Cytochromes in Chloroflexus aurantiacus grown with and without oxygen

Experiments measuring the initial uptake of commercial (³H) tetracycline exhibit two distinct kinetic phases: a rapid phase followed by a slow phase. (³H) tetracycline purified by chromatography on a Dowex 50WX2 column exhibited only monophasic rapid uptake when tested with susceptible Escherichia coli cells. Cyanide inhibited the uptake of purified (³H) tetracycline only partially while transport of proline and maltose was entirely abolished. Energy independent accumulation of tetracycline may be accounted for by binding to cellular constituents. Uptake of tetracycline-as measured by inhibition of -galactosidase synthesis-was strongly affected by a shift in temperature from 37°C to 21°C while carrier-mediated transport systems revealed only minor reductions. Taken together with the non-saturability of tetracycline uptake and the evidence for diffusion of tetracycline through phospholipid bilayers [Argast and Beck (1984) Antimicrob Agents Chemother 26:263–265] these data support the hypothesis that tetracycline enters the cytoplasm by diffusion.Abbreviations CCCP carbonyl cyanide m-chlorophenyl hydrazone - EDTA ethylenediaminetetraacetic acid - IPTG isopropyl--d-thiogalactopyranoside - NB nutrient broth - ONPG O-nitrophenyl--d-galactopyranoside     

Increased P diffusion as an explanation of increased p availability in flooded rice soils

Summary Phosphorus supply factors (capacity, kinetic, intensity, and diffusivity) and plant growth were the approaches used to assess P supply of flooded rice soils. Increases in the capacity, intensity, and kinetic factors, as measured by E-value, solution P concentration, and soil P release rate to a distilled water sink respectively, were unpronouced and infrequent upon water-saturation of ten soils. However, increases in the diffusitivity factor, as measured by ³²P diffusion coefficients, were at least ten-fold as soil moisture increased. The greatest increases in P diffusion occurred as soil moisture increased beyond one-third bar.Using a P fertilized soil or P treated powdered cellulose as the P source and a minus P nutrient solution to nourish a split root system with water and nutrients, data were obtained which suggested that P uptake and rice-shoot growth (indicators of P availability) increased with increasing moisture level. Phosphorus uptake and rice-shoot growth were greatst when the soil or P treated cellulose were water-saturated. These data indicate that increased soil P availability upon flooding can be attributed to an increase in the diffusivity factor.Paper Number 4532 of the Journal Series of the North Carolina Agricultural Experiment Station.Paper Number 4532 of the Journal Series of the North Carolina Agricultural Experiment Station.     

Ca2+ Sensitivity of Synaptic Vesicle Dopamine, γ-Aminobutyric Acid,and Glutamate Transport Systems

The effect of Ca2⁺ on the uptake of neurotransmitters by synaptic vesicles was investigated in a synaptic vesicle enriched fraction isolated from sheep brain cortex. We observed that dopamine uptake, which is driven at expenses of the proton concentration gradient generated across the membrane by the H⁺-ATPase activity, is strongly inhibited (70%) by 500 M Ca²⁺. Conversely, glutamate uptake, which essentially requires the electrical potential in the presence of low Cl^– concentrations, is not affected by Ca²⁺, even when the proton concentration gradient greatly contributes for the proton electrochemical gradient. These observations were checked by adding Ca²⁺ to dopamine or glutamate loaded vesicles, which promoted dopamine release, whereas glutamate remained inside the vesicles. Furthermore, similar effects were obtained by adding 150 M Zn²⁺ that, like Ca²⁺, dissipates the proton concentration gradient by exchanging with H⁺. With respect to -aminobutyric acid transport, which utilizes either the proton concentration gradient or the electrical potential as energy sources, we observed that Ca²⁺ or Zn²⁺ do not induce great alterations in the -aminobutyric acid accumulation by synaptic vesicles. These results clarify the nature of the energy source for accumulation of main neurotransmitters and suggest that stressing concentrations of Ca²⁺ or Zn²⁺ inhibit the proton concentration gradient-dependent neurotransmitter accumulation by inducing H⁺ pump uncoupling rather than by interacting with the neurotransmitter transporter molecules.     

The mismatch problem for GABAergic amacrine cells in goldfish retina: Resolution and other issues

GABAergic neurons in the vertebrate retina have received intensive study. Yet there are several notable examples of a mismatch among the cytochemical markers used to identify GABAergic neurons. The mismatch between [³H]GABA uptake autoradiography and all other indicators of GABAergic neurons as they pertain to amacrine cells in goldfish retina is examined in this overview. The discrepancies can be accounted for largely by barriers to diffusion presented by significant GABA uptake sinks at the inner and outer margins of the retina and by the differential subcellular distribution of the various markers for GABAergic neurons. Also, conditions producing a redistribution of [³H]-GABA and endogenous GABA stores within the retina are described and discussed.Special issue dedicated to Dr. Eugene Roberts