The synthesis of L-ascorbic acid in the rat from D-glucuronolactone and L-gulonolactone.

نویسندگان

  • J J BURNS
  • C EVANS
چکیده

Previous studies have shown that the intact carbon chain of glucose is utilized for the synthesis of L-ascorbic acid in the rat (l-3). Evidence for this precursor relationship came from experiments in which the administration of carbon land carbon 6-labeled glucose tracers resulted in the urinary excretion of n-ascorbic acid labeled predominantly in carbon 6 and carbon 1, respectively. Although these earlier studies were carried out in rats receiving Chloretone to increase their normal rate of L-ascorbic acid biosynthesis (4), recent results have shown that glucose is also a precursor of n-ascorbic acid in rats not treated with this drug (5). Two possible pathways for the biosynthesis of n-ascorbic acid from glucose in rats have been investigated. One, involving L-sorbose as an intermediate, was ruled out in a previous isotopic study (6). The other pathway involving n-glucuronolactone and n-gulonolactone as intermediates is shown in the accompanying scheme.

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Biological synthesis of L-ascorbic acid in animal tissues: conversion of L-gulonolactone into L-ascorbic acid.

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Biological synthesis of L-ascorbic acid in animal tissues: conversion of D-glucuronolactone and L-gulonolactone into L-ascorbic acid.

Simpson, S. A. & Tait, J. F. (1952). Endocrinology, 50, 150. Simpson, S. A. & Tait, J. F. (1953). Mem. Soc. Endocrin. 2,9. Southcott, C. M., Bandy, H. E., Newsom, S. E. & Darrach, M. (1956). Canad. J. Biochem. Phy8iol. 34, 913. Speirs, R. S. & Meyer, R. K. (1951). Endocrinology, 48, 316. Vogt, M. (1955). J. Physiol. 130, 601. Vogt, M. (1957). Ciba Foundation Colloq. Endocrin. 11, 193. Weichselb...

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عنوان ژورنال:
  • The Journal of biological chemistry

دوره 223 2  شماره 

صفحات  -

تاریخ انتشار 1956