Evidence for transmembrane electron transfer coupled to proton secretion in plasma membrane vesicles loaded by electroporation
- 46 Downloads
- 6 Citations
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 chainAbbreviations
- 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.
References
- 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
- 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
- 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
- — —, 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
- 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
- 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
- Böttger M (1986) Proton translocation systems at the plasmalemma and their possible regulation by auxin. Acta Hortic 179: 83–90Google Scholar
- —, Hilgendorf F (1988) Hormone action of transmembrane electron and H+ transport. Plant Physiol 86: 1038–1042Google Scholar
- —. Lüthen H (1986) Possible linkage between NADH oxidation and proton secretion inZea mays L. roots. J Exp Bot 37: 666–675Google Scholar
- —, Bigdon M, Soll HJ (1985) Proton translocation in corn coleoptiles: ATPase or redox chain. Planta 163: 376–380Google Scholar
- —, 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
- 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
- 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
- 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
- Craig TA, Crane FL (1981) Evidence for a transplasma membrane electron transport system in plant cells. Proc Indiana Acad Sci 90: 150–162Google Scholar
- 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
- 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
- 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
- Federico R, Giartosio CE (1983) A transplasma membrane electron transport system in maize root. Plant Physiol 73: 182–184Google Scholar
- 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
- 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
- —, 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
- 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
- Henderson LM, Chappell JB (1992) The NAPH-oxidase-associated H+ channel is opened by arachidonate. Biochem J 283: 171–175Google Scholar
- 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
- Knight DE, Scrutton MC (1986) Gaining access of the cytosol: the technique and some applications of electropermeabilization. Biochem J 234: 497–506Google Scholar
- 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
- 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
- Lundegardh H (1955) Mechanism of absorption, transport accumulation and secretion of ions. Annu Rev Plant Physiol 6: 1–24Google Scholar
- 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
- 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
- —, 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
- 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
- Marrè MT, Venegoni A, Moroni A (1992) Ethanol-induced activation of ATP-dependent proton inElodea densa leaves. Plant Physiol 100: 1120–1125Google Scholar
- 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
- —, 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
- 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
- — —, Curnutte JT (1993) Abnormal activation of H+ conductase in the NADPH oxidase-defective neutrophils. Proc Natl Acad Sci USA 90: 760–764Google Scholar
- 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
- Qiu ZS, Rubinstein B, Stern AI (1985) Evidence for electron transport across the plasma membrane ofZea mays root cells. Planta 165: 383–391Google Scholar
- Rensch C, Böttger M (1988) Localization of redox activity inZea mays roots. Mitt Inst Allg Bot Univ Hamburg 22: 5–17Google Scholar
- 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
- — —, Stout AG (1984) Redox activity at the surface of oat root cells. Plant Physiol 76: 386–391Google Scholar
- 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
- 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
- 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
- Stöhr C, Tischner R, Ward MR (1993) Characterization of the plasma-membrane-bound nitrate reductase inChlorella saccharophila (Krüger) Nadson. Planta 191: 79–85Google Scholar
- Sze H (1984) H+ translocating ATPase of the plasma membrane and tonoplast of plant cells. Physiol Plant 61: 683–691Google Scholar
- Vianello A, Macri F (1989) NAD(P)H oxidation elicits anion superoxide formation in radish plasmalemma vesicles. Biochim Biophys Acta 980: 202–208Google Scholar
- 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
- 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
- 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