Ascorbic acid (vitamin C) is an abundant component of plants. It reaches a
concentration of over 20 mM in chloroplasts and occurs in all cell compartm
ents, including the cell wall. It has proposed functions in photosynthesis
as an enzyme cofactor (including synthesis of ethylene, gibberellins and an
thocyanins) and in control of cell growth. A biosynthetic pathway via GDP-m
annose, GDP-L-galactose, L-galactose, and L-galactono-1,4-lactone has been
proposed only recently and is supported by molecular genetic evidence from
the ascorbate-deficient vtc1 mutant of Arabidopsis thaliana. Other pathways
via uronic acids could provide minor sources of ascorbate. Ascorbate, at l
east in some species, is a precursor of tartrate and oxalate. It has a majo
r role in photosynthesis, acting in the Mehler peroxidase reaction with asc
orbate peroxidase to regulate the redox stare of photosynthetic electron ca
rriers and as a cofactor for violaxanthin de-epoxidase, an enzyme involved
in xanthophyll cycle-mediated photoprotection. The hypersensitivity of some
of the vtc mutants to ozone and UV-B radiation, the rapid response of asco
rbate peroxidase expression to (photo)-oxidative stress, and the properties
of transgenic plants with altered ascorbate peroxidase activity all suppor
t an important antioxidative role for ascorbate. In relation to cell growth
, ascorbate is a cofactor for prolyl hydroxylase that posttranslationally h
ydroxylates proline residues in cell wail hydroxyproline-rich glycoproteins
required for cell division and expansion. Additionally, high ascorbate oxi
dase activity in the cell wall is correlated with areas of rapid cell expan
sion. It remains to he determined if this is a causal relationship and, if
so, what is the mechanism. Identification of the biosynthetic pathway now o
pens the way to manipulating ascorbate biosynthesis in plants, and, along w
ith the vtc mutants, this should contribute to a deeper understanding of th
e proposed functions of this multifacetted molecule.