Skip to main content
Log in

Stereospecificity and electrogenicity of amino acid transport in Riccia fluitans

  • Published:
Planta Aims and scope Submit manuscript

Abstract

In the aquatic liverwort Riccia fluitans, membrane depolarization (ΔΨm), change in membrane conductance (Δgm), and current-voltage (I-V) characteristics in the presence of different amino acids as well as the uptake of 14C-labeled amino acids were measured. L-isomers of the tested amino acids generate larger electrical effects (ΔΨm, Δgm) than D-isomers, and the I-V characteristics show that the positive electrical inward-current of 20 mA m-2 generated by 0.5 mM D-serine is only about 50% of the current generated by adding 0.5 mM L-serine. Whereas α- and β-amino acids rapidly depolarize the membrane to the same extend, with γ-aminobutyric acid (γ-AB) and dipeptides no significant electrical effects have been measured. The uptake kinetics of 14C-labeled amino acids display three components: (I) A saturable high-affinity component with Ks-values of 48 μM D-alanine, 12 μM α-aminoisobutyric acid (AIB), 9 μM L-alanine, 8 μM L-proline, and 6 μM L-serine, respectively; (2) an apparently linear low-affinity component, and (3) an also linear but unspecific component at concentrations >20 times the given Ks-value. Uptake of 14C-labeled AIB can be inhibited competitively by all tested neutral amino acids, the L-isomers being more effective than the D-isomers, as well as by ammonium or methylamine. Vice versa, AIB competitively inhibits uptake of L-serine and L-alanine. It is concluded that an uncharged stereospecific carrier for the investigated amino acids exists in the plasmalemma of Riccia fluitans. Accumulation ratios of about 50 suggest secondary active transport driven by a transmembrane electro-chemical gradient (mainly ΔΨm) which is generated by the electrogenic proton pump. It is suggested that this carrier binds to the amino group forming either a charged binary complex with positively charged amines (Felle 1980), or an uncharged complex with γ-AB or dipeptides, whereas electrogenic transport of α- and β-amino acids is mediated by a ternary carrier complex, probably charged by a proton.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

Ψm :

membrane potential (mV)

Eco :

equilibrium potential (mV) of the transport system

gm :

membrane (slope) conductance (Sm-2)

Δgm :

change in gm

I-V curve:

current-voltage curve

AIB:

α-aminoisobutytric acid

γ-AB:

γ-aminobutyric acid

References

  • Asghar, S.S., Levin, E., Harold, F.M. (1973) Accumulation of neutral amino acids by Streptococcus faecalis. Energy coupling by a proton-motive force. J. Biol. Chem. 248, 5225–5233

    Google Scholar 

  • Babcock, A.K., Garvey, T.Q. III, Berman, M. (1979). A mathemathical model for membrane transport of amino acids and Na+ in vesicles. J. Membrane Biol. 49, 157–169

    Google Scholar 

  • Bel, J.E.A. van, Erven, A. van (1976) Stimulation of proton influx by amino acid uptake in tomato internode discs. Z. Pflanzenphysiol. 80, 74–76

    Google Scholar 

  • Cheung, Y.-N.S., Nobel, P.S. (1973) Amino acid uptake by pea leaf fragments. Specificity, energy sources, and mechanism. Plant Physiol. 52, 633–637

    Google Scholar 

  • Christensen, H.N. (1975) Biological transport (2nd. ed.) W.A. Benjamin, Reading (Mass)

    Google Scholar 

  • Cohen, S.R. (1980) The complete rate equation, including the explicit dependence on Na+ ions, for the influx of α-amino-isobutyric acid into mouse brain slices. J. Membr. Biol. 52, 95–105

    Google Scholar 

  • Cole, K.S. (1968) Membrane, ions and impulses, pp. 152–168, University of California Press, Berkely

    Google Scholar 

  • Crane, R.K. (1962) Hypothesis for mechanism of intestinal active transport of sugars. Fed. Proc. 21, 891–895

    Google Scholar 

  • Crane, R.K. (1965) Na+-dependent transport in the intestine and other animal tissues. Fed. Proc. 24, 1000–1005

    Google Scholar 

  • Eddy, A.A., Novacki, J.A. (1971) Stoichiometrical proton and potassium ion movements accompanying the absorption of amino acids by the yeast Saccharomyces carlsbergensis. Biochem. J. 122, 701–711

    Google Scholar 

  • Etherton, B. (1978) Evidence for amino acid-H+ cotransport in oat coleoptiles. Plant Physiol. 61, 933–937

    Google Scholar 

  • Felle, H. (1980) Anine transport at the plasmalemma of Riccia fluitans. Biochim. Biophys. Acta. 602, 181–195

    Google Scholar 

  • Garvey, T.Q.III, Babcock, A. (1979) Amino acid and 22Na+-uptake in membrane vesicles from confluent simian virus 40 transformed Balb/c3T3 and Balb/c3T3. J. Membr. Biol. 49, 139–156

    Google Scholar 

  • Heinz, E., Geck, P., Pietrzyk, C. (1975) Driving forces of amino acid transport in animal cells. Ann. N.Y. Acad. Sci. 264, 428–441

    Google Scholar 

  • Hogg, J., Williams, E.J., Johnston, R.J. (1969) The membrane electrical parameters of Nitella translucens. Theor. Biol. 24, 317–334

    Google Scholar 

  • Jayakumar, A., Singh, M., Prasad, R. (1979) An inducible proline transport system in Candida albicans. Biochim. Biophys. Acta 556, 144–150

    Google Scholar 

  • Jung, K.-D., Lüttge, U. (1980) Amino acid uptake by Lemna gibba by a mechanism with affinity to neutral L- and D-amino acids. Planta 150, 230–235

    Google Scholar 

  • Kimmich, G.A., Randles, J. (1980) Evidence for an intestinal Na+: sugar transport coupling stoichiometry of 2.0. Biochim. Biophys. Acta 596, 439–444

    Google Scholar 

  • Komor, E., Tanner, W. (1971) Characterization of the active hexose transport system of Chlorella vulgaris. Biochim. Biophys. Acta 241, 170–179

    Google Scholar 

  • Komor, E., Tanner, W. (1974) The hexose-proton cotransport system of Chlorella: pH-dependent change in Km values and translocation constants of the uptake system. J. Gen. Physiol. 64, 568–581

    Google Scholar 

  • Mircheff, A.K., Os, C.H. van, Wright, E.M. (1980). Pathways for alanine transport in intestinal basal lateral membrane vesicles. J. Membr. Biol. 52, 83–92

    Google Scholar 

  • Mitchell, P. (1963) Molecule, group and electron translocation through natural membranes. Biochem. Soc. Symp. 22, 142–168

    Google Scholar 

  • Niven, D.F., Hamilton, W.A. (1974) Mechanisms of energy coupling to the transport of amino acids by Staphylococcus aureus. Eur. J. Biochem. 44, 517–522

    Google Scholar 

  • Pavlasova, E., Harold, F.M. (1969) Energy coupling in the transport of β-galactosides by E. coli: Effect of proton conductors. J. Bact. 98, 198–204

    Google Scholar 

  • Reinhold, L., Shtarkshall, R.A., Ganot, D. (1970) Transport of amino acids in barley leaf tissue. II. The kinetics of uptake of an unnatural analogue. J. Exp. Bot. 21, 926–932

    Google Scholar 

  • Riggs, T.R., Walker, L.M., Christensen, H.N. (1958) Potassium migration and amino acid transport. J. Biol. Chem. 233, 1479–1484

    Google Scholar 

  • Schultz, S.G., Curran, P.F. (1970) Coupled transport of sodium and organic solutes. Physiol. Rev. 50/4, 637–718

    Google Scholar 

  • Scaston, A., Inkston, C., Eddy, A.A. (1973) The absorption of protons with specific amino acids and carbohydrates by yeast. Biochem. J. 134, 1031–1043

    Google Scholar 

  • Slayman, C.L., Slayman, C.W. (1973) H+-dependent cotransport and the electrogenic pump in the plasma membrane of Neurospora. Abstr. Ann. Meeting Am. Soc. Microbiol. Item P 189

  • Slayman, C.L., Slayman, C.W. (1974) Depolarization of the plasma membrane of Neurospora during active transport of glucose: Evidence for a proton-dependent cotransport system. Proc. Natl. Acad. Sci. USA 71/5, 1935–1939

    Google Scholar 

  • Slayman, C.L., Slayman, C.W., Hansen, U.-P. (1977) In: Transmembrane ionic exchanges in plants, pp. 115–122, Thellier, M., Monnier, A., Demarty, M., Dainty, J. eds. CNRS, Paris

    Google Scholar 

  • Steinmüller, F., Bentrup, F.W. (1981) Amino acid transport in photoautotrophic suspension cells of Chenopodium rubrum L.: Stereospecificity and interaction with potassium ions. Z. Pflanzenphysiol. (in press)

  • West, I.C. (1970) Lacrose transport coupled to proton movements in Escherichia coli. Biochem. Biophys. Res. Comm. 41, 655–661

    Google Scholar 

  • West, I.C., Mitchell, P. (1973) Stoichiometry of lactose-H+-symport across the plasma membrane of Escherichia coli. Biochem. J. 132, 587–592

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Felle, H. Stereospecificity and electrogenicity of amino acid transport in Riccia fluitans . Planta 152, 505–512 (1981). https://doi.org/10.1007/BF00380821

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00380821

Key words

Navigation