Protoplasma

, Volume 184, Issue 1–4, pp 22–30 | Cite as

Evidence for transmembrane electron transfer coupled to proton secretion in plasma membrane vesicles loaded by electroporation

  • M. Böttger
  • D. J. Morré
  • F. L. Crane
Article

Summary

We demonstrate an in vitro trans plasma membrane electron transport from an encapsulated nucleotide to an external electron acceptor. Right-side-out vesicles prepared from soybean hypocotyls by aqueous two-phase partitioning were loaded with NADH by electroporation. Absence of calcium ions and an electric field strength of over 2 kV/cm was necessary for opening of the vesicles and importation of NADH. The presence of calcium ions was necessary for vesicle sealing. External NADH was removed with oxalacetate and malate dehydrogenase. If an impermeable electron acceptor was added to the exterior of the sealed vesicles, the oxidation of encapsulated NADH was increased, indicating a transmembrane electron transfer from an internal e donor to the external e acceptor analogous to that observed with intact cells. The ratio of NADH oxidized to hexacyanoferrat III reduced was 0.67. This indicates that NADH oxidation with oxygen as acceptor still occurred. Oxidation of the internal NADH was not affected by cyanide, azide, SOD or catalase but was inhibited by actinomycin D. Inhibition was also observed by the auxin 2,4-D, but by the inactive analog 2,3-D too. Oxidation of internal NADH both in absence and presence of the external acceptor, HCF III, showed a rapid decline in activity, which is relieved by the detergent Triton X-100, or the protonophore FCCP. Maximum NADH oxidation both with and without HCF III required an internal acidic pH gradient across the vesicle membrane. The results are consistent with a proton-gradient driving transplasma membrane NADH dehydrogenase which can transfer electrons to oxygen or an external impermeable oxidant.

Keywords

NADH oxidation Plasma membrane Proton transport Redox chain 

Abbreviations

bis propane

1,3 bis(tris(hydroxymethyl) methylamino) propane

BHA

2(3)-tert-butyl-4-hydroxyanisol

FCCP

carbonyl cyanide-p-trifluoromethoxy-phenylhydrazone

MES

morpholino-ethan sulfonic acid

HCF

III hexacyanoferrat III (“ferricyanide”)

MDH

malate dehydrogenase

OAA

oxalacetate

PMSF

phenylmethylsulfonylfluoride

SOD

Superoxide dismutase

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Apostol I, Heinstein PF, Low PS (1989) Rapid stimulation of an oxidative burst during elicitation of cultured plant cells. Plant Physiol 90: 109–115Google Scholar
  2. Asard H, Horemans N, Caubergs RJ (1992) Transmembrane electron transport in ascorbate loaded plasma membrane vesicles from higher plants involved ab-type cytochrome FEBS Lett 306: 143–146Google Scholar
  3. Askerlund P, Larrson C (1991) Redox activities measured with inside-out and right-side-out plasma membrane vesicles from sugar beet leaves. Plant Physiol 96: 1178–1184Google Scholar
  4. — —, Widell S (1988) Localization of donor and acceptor sides of NADH dehydrogenase activities using inside-out and rightside-out plasma membrane vesicles from plants. FEBS Lett 239: 23–28Google Scholar
  5. Barr R, Sandelius AS, Crane FL, Morré DJ (1986) Redox reactions of tonoplast and plasma membranes isolated from soybeans hypocotyls by free-flow electrophoresis. Biochim Biophys Acta 852: 254–261Google Scholar
  6. Bienfait F, Lüttge U (1988) On the function of two systems that can transfer electrons across the plasma membrane. Plant Physiol Biochem 26: 665–671Google Scholar
  7. Böttger M (1986) Proton translocation systems at the plasmalemma and their possible regulation by auxin. Acta Hortic 179: 83–90Google Scholar
  8. —, Hilgendorf F (1988) Hormone action of transmembrane electron and H+ transport. Plant Physiol 86: 1038–1042Google Scholar
  9. —. Lüthen H (1986) Possible linkage between NADH oxidation and proton secretion inZea mays L. roots. J Exp Bot 37: 666–675Google Scholar
  10. —, Bigdon M, Soll HJ (1985) Proton translocation in corn coleoptiles: ATPase or redox chain. Planta 163: 376–380Google Scholar
  11. —, Döring O, Barr R, Brightman AO, Morré DJ, Crane FL (1993) Calmodulin inhibitors on NADH oxidation by isolated plasma membrane vesicles preloaded with NADH. Plant Sci 87: 39–44Google Scholar
  12. Bradley DJ, Kjellbom P, Lamb CJ (1992) Elicitor- and wound-induced oxidative cross-linking of a proline-rich plant cell wall protein: a novel, rapid defense response. Cell 70: 21–30Google Scholar
  13. Brightman AO, Barr R, Crane FL, Morré DJ (1988) Auxin-stimulated NADH oxidase purified from plasma membrane of soybeans. Plant Physiol 86: 1264–1269Google Scholar
  14. Buckhout TJ, Hrubec TC (1986) Pyridine nucleotide dependent ferricyanide reduction associated with isolated plasma membranes of maize (Zea mays) roots. Protoplasma 135: 144–154Google Scholar
  15. Craig TA, Crane FL (1981) Evidence for a transplasma membrane electron transport system in plant cells. Proc Indiana Acad Sci 90: 150–162Google Scholar
  16. Dancis A, Roman DG, Anderson GI, Hinnebusch AG, Klausner RD (1992) Ferric reductase ofSaccharomyces cerevisiae: molecular characterization, role in iron uptake, and transcriptional control by iron. Proc Natl Acad Sci USA 89: 3869–3873Google Scholar
  17. Doke N, Ohashi Y (1988) Involvement of an O2-generating system in the induction of necrotic lesions on tobacco leaves infected with tobacco mosaic virus. Physiol Plant Pathol 32: 163–175Google Scholar
  18. Döring O, Lüthje S, Hilgendorf F, Büttger M (1990) Membrane depolarization by hexacyanoferrate (III), hexabromoiridate (IV) and hexachloroiridate (IV). J Exp Bot 41: 1055–1061Google Scholar
  19. Federico R, Giartosio CE (1983) A transplasma membrane electron transport system in maize root. Plant Physiol 73: 182–184Google Scholar
  20. Gianini JL, Briskin DP (1988) Pyridine nucleotide oxidation by a plasma membrane fraction from red beet (Beta vulgaris L.) storage tissue. Arch Biochem Biophys 260: 653–660Google Scholar
  21. Grabov A, Böttger M (1994) Are redox reaction involved in the regulation of K+ channels in the plasma membrane ofLimnobium stoloniferum root hairs? Plant Physiol 105: 927–935Google Scholar
  22. —, Felle H, Böttger M (1993) Implication of cytosolic pH on the activation of plasma membrane proton pumps and electron transfer. J Exp Bot 44: 725–730Google Scholar
  23. Hassidim M, Rubinstein B, Lerner HR, Reinhold L (1987) Generation of a membrane potential by electron transport in plasmalemma-enriched vesicles of cotton and radish. Plant Physiol 85: 872–875Google Scholar
  24. Henderson LM, Chappell JB (1992) The NAPH-oxidase-associated H+ channel is opened by arachidonate. Biochem J 283: 171–175Google Scholar
  25. Hilgendorf F, Böttger M (1993) Influence of temperature on proton secretion and hexacyanoferrat (III) reduction ofZea mays L. roots. Plant Physiol 101: 1349–1353Google Scholar
  26. Knight DE, Scrutton MC (1986) Gaining access of the cytosol: the technique and some applications of electropermeabilization. Biochem J 234: 497–506Google Scholar
  27. Krüger S, Böttger M (1989) NADH or NADPH? In: Crane FL, Morré DJ, Löw H (eds) Plasma membrane oxidoreductases in control of animal and plant growth. Plenum, New York, pp 105–114Google Scholar
  28. Löppert H (1983) Energy coupling for membrane hyperpolarization inLemna: respiration rate, ATP level and membrane potential at low oxygen concentrations. Planta 159: 329–335Google Scholar
  29. Lundegardh H (1955) Mechanism of absorption, transport accumulation and secretion of ions. Annu Rev Plant Physiol 6: 1–24Google Scholar
  30. Lüthje S, Böttger M (1989) Hexabromoiridate IV as an electron acceptor: comparison with hexachloroiridate IV and hexacyanoferrate III. Biochim Biophys Acta 977: 335–340Google Scholar
  31. Macri F, Vianello A (1986) Independence of transplasma membrane proton gradient from NAD(P) ferricyanide oxidoreduction in maize root microsomes. Plant Sci 43: 25–29Google Scholar
  32. —, Braidor E, Petrussa E, Zankani M, Vianello A (1992) Ferric ion and oxygen reduction at the surface of protoplasts and cells ofAcer pseudoplatanus. Bot Acta 105: 97–103Google Scholar
  33. Marrè MT, Moroni A, Albergoni FG, Marré E (1988) Activation of the H+ pump by ferricyanide-induced potential depolarization and cytoplasm acidification. Plant Physiol 87: 25–30Google Scholar
  34. Marrè MT, Venegoni A, Moroni A (1992) Ethanol-induced activation of ATP-dependent proton inElodea densa leaves. Plant Physiol 100: 1120–1125Google Scholar
  35. Morrè DJ, Navas P, Penel C, Castillo FJ (1986) Auxin-stimulated NADH oxidase (semidehydroascorbate reductase) of soybean plasma membrane: role in acidification of cytoplasm? Protoplasma 133: 195–197Google Scholar
  36. —, Auderset G, Penel C, Canut H (1987) Cytochemical localization of NADH ferricyanide oxido-reductase in hypocotyl segments and isolated membrane vesicles of soybean. Protoplasma 140: 133–140Google Scholar
  37. Nanda A, Grinstein S (1991) Protein kinase C activates an H+ (equivalent) conductance in the plasma membrane of human neutrophils. Proc Natl Acad Sci USA 88: 10816–10820Google Scholar
  38. — —, Curnutte JT (1993) Abnormal activation of H+ conductase in the NADPH oxidase-defective neutrophils. Proc Natl Acad Sci USA 90: 760–764Google Scholar
  39. Neumann E, Schäfer-Ridder M, Wang Y, Hofschneider PH (1982) Gene transfer into mouse lyoma cells by electroporation in high electric fields. EMBO J 7: 841–845Google Scholar
  40. Qiu ZS, Rubinstein B, Stern AI (1985) Evidence for electron transport across the plasma membrane ofZea mays root cells. Planta 165: 383–391Google Scholar
  41. Rensch C, Böttger M (1988) Localization of redox activity inZea mays roots. Mitt Inst Allg Bot Univ Hamburg 22: 5–17Google Scholar
  42. Rubinstein B, Stern AI (1986) Relationship of transplasmalemma redox activity to proton and solute transport by roots ofZea mays. Plant Physiol 80: 805–811Google Scholar
  43. — —, Stout AG (1984) Redox activity at the surface of oat root cells. Plant Physiol 76: 386–391Google Scholar
  44. Sandelius AS, Barr R, Crane FL, Morré DL (1986) Redox reaction of plasma membranes isolated from soybean hypocotyls by phase partition. Plant Sci 48: 1–10Google Scholar
  45. Serrano R (1987) The proton pumping ATPase of yeast plasma membranes is essential for growth: redox pumps may not be physiologically significant. In: Ramirez JM (ed) Redox functions of the eukaryotic plasma membrane. Consejo Superior de Investigaciones Cientificas, Madrid, pp 19–26Google Scholar
  46. Sijmons PC, van den Briel J, Bienfait HF (1984) Cytosolic NADPH is the electron donor for extracellular Fe3+ reduction in iron deficient bean roots. Plant Physiol 75: 219–222Google Scholar
  47. Stöhr C, Tischner R, Ward MR (1993) Characterization of the plasma-membrane-bound nitrate reductase inChlorella saccharophila (Krüger) Nadson. Planta 191: 79–85Google Scholar
  48. Sze H (1984) H+ translocating ATPase of the plasma membrane and tonoplast of plant cells. Physiol Plant 61: 683–691Google Scholar
  49. Vianello A, Macri F (1989) NAD(P)H oxidation elicits anion superoxide formation in radish plasmalemma vesicles. Biochim Biophys Acta 980: 202–208Google Scholar
  50. Ward MR, Tischner R, Huffaker RC (1988) Inhibition of nitrate transport by anti-nitrate reductase IgG fragments and the identification of plasma membrane associated reductase in roots of barley seedlings. Plant Physiol 88: 1141–1146Google Scholar
  51. Welch RM, Norvell WA, Schaefer SC, Shaff JE, Kochian LV (1993) Induction of iron (III) and copper (II) reduction in pea (Pisum sativum L.) roots by Fe and Cu status: does the root-cell plasmalemma Fe(III)-chelate reductase perform a general role in regulating cation uptake? Planta 190: 555–561Google Scholar
  52. Yoshida S, Kawata T, Uemura M, Niki T (1986) Properties of plasma membrane isolated from chilling-sensitive etiolated seedlings ofVigna radiata L. Plant Physiol 80: 152–160Google Scholar

Copyright information

© Springer-Verlag 1995

Authors and Affiliations

  • M. Böttger
    • 1
  • D. J. Morré
    • 2
  • F. L. Crane
    • 3
  1. 1.Institut für Allgemeine BotanikUniversität HamburgHamburgFederal Republic of Germany
  2. 2.Department of Medicinal ChemistryPurdue UniversityWest Lafayette
  3. 3.Department of Biological SciencesPurdue UniversityWest Lafayette

Personalised recommendations