Journal of Bioenergetics and Biomembranes

, Volume 26, Issue 4, pp 369–377

Dehydroascorbate reduction

  • William W. Wells
  • Dian Peng Xu

DOI: 10.1007/BF00762777

Cite this article as:
Wells, W.W. & Xu, D.P. J Bioenerg Biomembr (1994) 26: 369. doi:10.1007/BF00762777


Dehydroascorbic acid is generated in plants and animal cells by oxidation of ascorbic acid. The reaction is believed to occur by the one-electron oxidation of ascorbic acid to semidehydroascorbate radical followed by disproportionation to dehydroascorbic acid and ascorbic acid. Semidehydroascorbic acid may recycle to ascorbic acid catalyzed by membrane-bound NADH-semidehydroscorbate reductase. However, disproportionation of the free radical occurs at a rapid rate, 105 M−1 s−1, accounting for measurable cellular levels of dehydroascorbate. Dehydroascorbate reductase, studied earlier and more extensively in plants, is now recognized as the intrinsic activity of thioltransferases (glutaredoxins) and protein disulfide isomerase in animal cells. These enzymes catalyze the glutathione-dependent two-electron regeneration of ascorbic acid. The importance of the latter route of ascorbic acid renewal was seen in studies of GSH-deficient rodents (Meister, A. (1992)Biochem. Pharmacol.44 1905–1915). GSH deficiency in newborn animals resulted in decreased tissue ascorbic acid and increased dehydroascorbate-to-ascorbate ratios. Administration of ascorbic acid daily to GSH-deficient animals decreased animal mortality and cell damage from oxygen stress. A cellular role is proposed for dehydroascorbate in the oxidation of nascent protein dithiols to disulfides catalyzed in the endoplasmic reticulum compartment by protein disulfide isomerase.

Key words

Dehydroascorbic acidascorbic acidsemidehydroascorbic acidglutathioneglutathione: dehydroascorbate oxidoreductaseNADH semidehydroascorbate reductasel-buthionine-SR-sulfoximinegastric ascorbateprotein disulfide bondsprotein disulfide isomerase

Copyright information

© Plenum Publishing Corporation 1994

Authors and Affiliations

  • William W. Wells
    • 1
  • Dian Peng Xu
    • 1
  1. 1.Department of BiochemistryMichigan State UniversityEast Lansing