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. 1994 Sep;106(1):187–193. doi: 10.1104/pp.106.1.187

Transport of Ascorbic and Dehydroascorbic Acids across Protoplast and Vacuole Membranes Isolated from Barley (Hordeum vulgare L. cv Gerbel) Leaves.

AAF Rautenkranz 1, L Li 1, F Machler 1, E Martinoia 1, J J Oertli 1
PMCID: PMC159515  PMID: 12232318

Abstract

Protoplasts, vacuoles, and chloroplasts were isolated from leaves of 8-d-old barley (Hordeum vulgare L. cv Gerbel) seedlings. Transport of ascorbate and dehydroascorbate into protoplasts and vacuoles was investigated. Contents of ascorbic acid, glutathione, and [alpha]-tocopherol and ascorbate peroxidase activity and glutathione reductase activity were analyzed in protoplasts, vacuoles, and chloroplasts. Uptake of ascorbate and dehydroascorbate by protoplasts showed saturation kinetics (Km = 90 [mu]M reduced ascorbic acid, 20 [mu]M dyhydroascorbic acid). Effects of various membrane transport inhibitors suggested that transport was carrier mediated and driven by a proton electrochemical gradient. Translocation of ascorbate and dehydroascorbate into vacuoles did not show saturation kinetics. Neither was it influenced by effectors or by ATP but only by Mg2+, suggesting that translocation did not occur by carrier. Ascorbic acid was predominantly localized in the cytosol. Contents in the chloroplasts and vacuoles were low. The results are consistent with the view that ascorbate is synthesized in the cytosol and released to chloroplasts, apoplast, and vacuole following a concentration gradient. Translocation from the apoplast into the cytosol is against a steep gradient and appears to control the concentration of ascorbic acid in the apoplast. In its function as an antioxidant, ascorbate in the apoplast may be oxidized to dehydroascorbate, which can be efficiently transported back into the cytosol for regeneration to ascorbate.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Beck E., Burkert A., Hofmann M. Uptake of l-Ascorbate by Intact Spinach Chloroplasts. Plant Physiol. 1983 Sep;73(1):41–45. doi: 10.1104/pp.73.1.41. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bianchi J., Wilson F. A., Rose R. C. Dehydroascorbic acid and ascorbic acid transport systems in the guinea pig ileum. Am J Physiol. 1986 Apr;250(4 Pt 1):G461–G468. doi: 10.1152/ajpgi.1986.250.4.G461. [DOI] [PubMed] [Google Scholar]
  3. Bowman E. J., Siebers A., Altendorf K. Bafilomycins: a class of inhibitors of membrane ATPases from microorganisms, animal cells, and plant cells. Proc Natl Acad Sci U S A. 1988 Nov;85(21):7972–7976. doi: 10.1073/pnas.85.21.7972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Luwe MWF., Takahama U., Heber U. Role of Ascorbate in Detoxifying Ozone in the Apoplast of Spinach (Spinacia oleracea L.) Leaves. Plant Physiol. 1993 Mar;101(3):969–976. doi: 10.1104/pp.101.3.969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. MARTIN G. R. Studies on the tissue distribution of ascorbic acid. Ann N Y Acad Sci. 1961 Apr 21;92:141–147. doi: 10.1111/j.1749-6632.1961.tb46113.x. [DOI] [PubMed] [Google Scholar]
  6. Rose R. C. Solubility properties of reduced and oxidized ascorbate as determinants of membrane permeation. Biochim Biophys Acta. 1987 Apr 16;924(1):254–256. doi: 10.1016/0304-4165(87)90094-8. [DOI] [PubMed] [Google Scholar]
  7. WILKINSON G. N. Statistical estimations in enzyme kinetics. Biochem J. 1961 Aug;80:324–332. doi: 10.1042/bj0800324. [DOI] [PMC free article] [PubMed] [Google Scholar]

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