l-Tartaric acid synthesis from vitamin C in higher plants
- *School of Agriculture, Food, and Wine, University of Adelaide, Adelaide, SA 5005, Australia;
- †Department of Plant Pathology, University of California, Davis, CA 95616-8680; and
- ‡Cooperative Research Centre for Viticulture, P.O. Box 145, Glen Osmond, SA 5064, Australia
-
Edited by Luis Herrera-Estrella, National Polytechnic Institute, Guanajuato, Mexico, and approved February 3, 2006 (received for review December 15, 2005)
Abstract
The biosynthetic pathway of l-tartaric acid, the form most commonly encountered in nature, and its catabolic ties to vitamin C, remain a challenge to plant scientists. Vitamin C and l-tartaric acid are plant-derived metabolites with intrinsic human value. In contrast to most fruits during development, grapes accumulate l-tartaric acid, which remains within the berry throughout ripening. Berry taste and the organoleptic properties and aging potential of wines are intimately linked to levels of l-tartaric acid present in the fruit, and those added during vinification. Elucidation of the reactions relating l-tartaric acid to vitamin C catabolism in the Vitaceae showed that they proceed via the oxidation of l-idonic acid, the proposed rate-limiting step in the pathway. Here we report the use of transcript and metabolite profiling to identify candidate cDNAs from genes expressed at developmental times and in tissues appropriate for l-tartaric acid biosynthesis in grape berries. Enzymological analyses of one candidate confirmed its activity in the proposed rate-limiting step of the direct pathway from vitamin C to tartaric acid in higher plants. Surveying organic acid content in Vitis and related genera, we have identified a non-tartrate-forming species in which this gene is deleted. This species accumulates in excess of three times the levels of vitamin C than comparably ripe berries of tartrate-accumulating species, suggesting that modulation of tartaric acid biosynthesis may provide a rational basis for the production of grapes rich in vitamin C.
Footnotes
- §To whom correspondence should be addressed. E-mail: christopher.ford{at}adelaide.edu.au
-
Author contributions: S.D., D.R.C., and C.M.F. designed research; S.D. and C.M.F. performed research; D.R.C. contributed new reagents/analytic tools; S.D. and D.R.C. analyzed data; and S.D., D.R.C., and C.M.F. wrote the paper.
-
Conflict of interest statement: No conflicts declared.
-
This paper was submitted directly (Track II) to the PNAS office.
-
Data deposition: The sequence reported in this paper has been deposited in the GenBank database (accession no. DQ124868).
- Abbreviations:
- TA,
- l-tartaric acid;
- AA,
- l-ascorbic acid;
- OxA,
- oxalic acid;
- l-IdnDH,
- l-idonate dehydrogenase.
Abbreviations:
- © 2006 by The National Academy of Sciences of the USA





