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Transport of ascorbate into protoplasts ofNicotiana tabacum Bright Yellow-2 cell line

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Summary

The uptake of ascorbate into protoplasts isolated from aNicotiana tabacum Bright Yellow-2 (BY-2) cell suspension culture was investigated. Addition of14C-labelled ascorbate to freshly isolated protoplasts resulted in a time- and substrate-dependent association of radioactive molecules with the protoplasts. The kinetic characterisation of this presumptive uptake revealed kinetics of Michaelis-Menten type with an apparent maximal uptake activity of 24 pmol/min·106 protoplasts and an apparent affinity constant of 139 μM. The amount of ascorbate molecules transported intoN. tabacum protoplasts decreased when nonlabelled dehydroascorbate or iso-ascorbate were added but was not affected by addition of 5,6-o-cyclohexylidene ascorbate or ascorbate-2-sulfate. These data indicate a carrier-mediated uptake of ascorbate into the protoplasts that shows a high structural specificity. To investigate which redox status of ascorbate is preferentially taken up by theN. tabacum protoplasts, transport was tested in the presence of various compounds that can affect the redox status of ascorbate. Testing uptake in the presence of a reductant, dithiothreitol, resulted in a significant and concentration-dependent inhibition of the amount of ascorbate molecules transported into the protoplasts. On the other hand, ascorbate uptake was significantly stimulated in the presence of the enzyme ascorbate oxidase. Ferricyanide did not affect ascorbate transport. Inhibition studies revealed that ascorbate uptake in the protoplasts is sensitive to addition of sulfhydryl reagents N-ethyl maleimide andp-chloro-mercuribenzenesulfonic acid and to a disruption of the proton gradient by the protonophore carbonylcyanide-3-chlorophenylhydrazone. The uptake of ascorbate was also inhibited by addition of cytochalasin B but not sensitive to addition of phloretin or sulfinpyrazone. Taken together these data indicate the presence of an ascorbate transport system in the plasma membrane ofN. tabacum protoplasts and suggest dehydroascorbate as the preferentially transported redox species. The putative presence of different carriers for reduced and oxidised ascorbate in the plasma membrane is discussed.

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Abbreviations

Asc:

ascorbate

BY-2:

Bright Yellow 2

CCCP:

carbonylcyanide-3-chlorophenylhydrazone

DHA:

dehydroascorbate

DTT:

dithiothreitol

MS:

medium Murashige and Skoog medium

NEM:

N-ethylmaleimide

pCMBS:

p-chloromercuribenzenesulfonic acid

References

  • Castillo FJ, Greppin H (1988) Extracellular ascorbic acid and enzyme activities related to ascorbic acid metabolism inSedum alba L. leaves after ozone exposure. Environ Exp Bot 28: 231–238

    Google Scholar 

  • Chupakhina ON, Kuznetsova LG, Kovaleva NA (1994) Light-dependent accumulation of ascorbic acid and its derivatives in barley leaves in the presence of protein synthesis inhibitors. Russ J Plant Physiol 41: 19–23

    Google Scholar 

  • Citterio S, Sgorbati S, Scippa S, Sparvoli E (1994) Ascorbic acid effect on the onset of cell proliferation in pea root. Physiol Plant 92: 601–607

    Google Scholar 

  • De Cabo RC, Gonzalez-Reyes JA, Navas P (1993) The onset of cell proliferation is stimulated by ascorbate free radical in onion root primordia. Biol Cell 77: 231–233

    Google Scholar 

  • Foyer CH, Halliwell B (1976) Presence of glutathione and gluthatione reductase in chloroplasts: a proposed role in ascorbic acid metabolism. Planta 133: 21–25

    Google Scholar 

  • —, Lelandais M (1996) A comparison of the relative rates of transport of ascorbate and glucose across the thylakoid, chloroplast and plasmalemma membranes of pea leaf mesophyll cells. J Plant Physiol 148: 391–398

    Google Scholar 

  • —, Rowell J, Walker DA (1983) Measurements of the ascorbate content of spinach leaf protoplasts and chloroplasts during illumination. Planta 157: 239–244

    Google Scholar 

  • —, Lelandais M, Kunert KJ (1994) Photooxidative stress in plants. Physiol Plant 92: 696–717

    Google Scholar 

  • Franceschi RT, Wilson JX, Dixon SJ (1995) Requirement for Na+-dependent ascorbic acid transport in osteoblast function. Am J Physiol 268 (Cell Physiol 37): C1430-C1439

    Google Scholar 

  • Goldenberg H, Schweinzer E (1994) Transport of vitamin C in animal and human cells. J Bioenerg Biomembr 26: 359–367

    Google Scholar 

  • González-Reyes JA, Alcain FJ, Caler JA, Serrano A, Cordoba F, Navas P (1994) Relationship between apoplastic ascorbate regeneration and the stimulation of root growth inAllium cepa L. Plant Sci 100: 23–29

    Google Scholar 

  • Hidalgo A, Garcia-Herdugo G, Gonzalez-Reyes JA, Morré DJ, Navas P (1991) Ascorbate free radical stimulates onion root growth by increasing cell elongation. Bot Gaz 152: 282–288

    Google Scholar 

  • Horemans N, Asard H, Caubergs RJ (1996) Transport of ascorbate into plasma membrane vesicles ofPhaseolus vularis L. Protoplasma 194: 177–185

    Google Scholar 

  • — — — (1997) The ascorbate carrier of higher plant plasma membranes preferentially translocates the fully oxidized (dehydroascorbate) molecule. Plant Physiol 114: 1247–1253

    Google Scholar 

  • — — — (1998) Carrier mediated uptake of dehydroascorbate into higher plant plasma membrane vesicles shows trans-stimulation. FEBS Lett 421: 41–44

    Google Scholar 

  • Katz DB, Sussman MR (1987) Inhibition and labeling of the plant H+-ATPase with N-ethylmaleimide. Plant Physiol 83: 977–981

    Google Scholar 

  • Luwe M (1996) Antioxidants in the apoplast and symplast of beech (Fagus sylvatica L.) leaves: seasonal variations and responses to changing ozone concentration in air. Plant Cell Environ 19: 321–328

    Google Scholar 

  • —, Heber U (1995) Ozone detoxification in the apoplasm and symplasm of spinach, broad bean and beech leaves at ambient and elevated concentrations of ozone in air. Planta 197: 448–455

    Google Scholar 

  • —, Takahama U, Heber U (1993) Role of ascorbate in detoxifying ozone in the apoplast of spinach (Spinacia oleracea L.) leaves. Plant Physiol 101: 969–976

    Google Scholar 

  • Maffia M, Ahearn GA, Vilella V, Anno V, Storelli C (1993) Ascorbic acid transport by intestinal brush-border membrane vesicles of teleostAnuilla anuilla. Am J Physiol 264: R1248-R1253

    Google Scholar 

  • Mozafar A, Oertli JJ (1993) Vitamin C (ascorbic acid): uptake and metabolism by soybean. J Plant Physiol 141: 316–321

    Google Scholar 

  • Murashige T, Skoog F (1962) A revised medium for rapid growth and bioassay with tobacco tissue cultures. Physiol Plant 15: 473–496

    Google Scholar 

  • Nagata T, Nemoto Y, Hasezawa S (1992) Tobacco BY-2 cell line as the “HeLa” cell in the cell biology of higher plants. Int Rev Cytol 132: 1–30

    Google Scholar 

  • Navarro F, Rodriguez-Anguilera JC, Alcain FJ, Buron MI, Navas P (1992) Ascorbate potentiates serum-induced S phase entry of quiescent 3T3 cells. Protoplasma 169: 85–87

    Google Scholar 

  • Ngkeekwong FC, Ng LL (1997) Two distinct uptake mechanisms for ascorbate and dehydroascorbate in human lymphoblasts and their interaction with glucose. Biochem J 324: 225–230

    Google Scholar 

  • Polle A, Chakrabarti K, Schumann W, Rennenberg H (1990) Composition and properties of hydrogen peroxide decomposing systems in extracellular and total extracts from needles of Norway spruce (Picea abies L., Karst.). Plant Physiol 94: 312–319

    Google Scholar 

  • Rautenkranz AAF, Li L, Mächler F, Märtinoia E, Oertli JJ (1994) Transport of ascorbic and dehydroascorbic acids across protoplast and vacuole membranes isolated from barley (Hordeum vulgare L. cv Gerbel) leaves. Plant Physiol 106: 187–193

    Google Scholar 

  • Rose RC (1988) Transport of ascorbic acid and other water-soluble vitamins. Biochim Biophys Acta 947: 335–366

    Google Scholar 

  • Smirnoff N (1996) The function and metabolism of ascorbic acid in plants. Ann Bot 78: 661–669

    Google Scholar 

  • Takahama U, Oniki T (1992) Regulation of peroxidase-oxidation of phenolics in the apoplast of spinach leaves by ascorbate. Plant Cell Physiol 33: 379–387

    Google Scholar 

  • Vera JC, Rivas CI, Fischbarg J, Golde DW (1993) Mammalian facultative hexose transporters mediate the transport of dehydroascorbic acid. Nature 364: 79–82

    Google Scholar 

  • Wolf G (1996) The mechanism of uptake of ascorbic acid into osteoblasts and leukocytes. Nutr Rev 54: 150–152

    Google Scholar 

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Horemans, N., Potters, G., Caubergs, R.J. et al. Transport of ascorbate into protoplasts ofNicotiana tabacum Bright Yellow-2 cell line. Protoplasma 205, 114–121 (1998). https://doi.org/10.1007/BF01279301

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