Plant Physiol, December 1999, Vol. 121, pp. 1281-1290
Proline Metabolism in the Wild-Type and in a Salt-Tolerant Mutant
of Nicotiana plumbaginifolia Studied by
13C-Nuclear Magnetic Resonance Imaging1
Nancy H.
Roosens,*
Rudolph
Willem,
Yan
Li,
Ingrid
Verbruggen,
Monique
Biesemans, and
Michel
Jacobs
Laboratory of Plant Genetics, Institute of Molecular Biology, Free
University of Brussels, Paardenstraat 65, B-1640
Sint-Genesius-Rode, Belgium (N.H.R., Y.L., M.B., M.J.); and High
Resolution NMR Centre Pleinlaan 2, B-1050 Brussel, Belgium (R.W.,
I.V., M.B.)
To obtain insight into the link
between proline (Pro) accumulation and the increase in osmotolerance in
higher plants, we investigated the biochemical basis for the NaCl
tolerance of a Nicotiana plumbaginifolia mutant (RNa)
that accumulates Pro. Pro biosynthesis and catabolism were investigated
in both wild-type and mutant lines. 13C-Nuclear magnetic
resonance with [5-13C]glutamate (Glu) as the Pro
precursor was used to provide insight into the mechanism of Pro
accumulation via the Glu pathway. After 24 h under 200 mM NaCl stress in the presence of [5-13C]Glu,
a significant enrichment in [5-13C]Pro was observed
compared with non-stress conditions in both the wild type (P2) and the
mutant (RNa). Moreover, under the same conditions,
[5-13C]Pro was clearly synthesized in higher amounts in
RNa than in P2. On the other hand, measurements of enzyme activities
indicate that neither the biosynthesis via the ornithine pathway, nor
the catabolism via the Pro oxidation pathway were affected in the RNa
mutant. Finally, the regulatory effect exerted by Pro on its biosynthesis was evaluated. In P2 plantlets, exogenous Pro markedly reduced the conversion of [5-13C]Glu into
[5-13C]Pro, whereas Pro feedback inhibition was not
detected in the RNa plantlets. It is proposed that the origin of
tolerance in the RNa mutant is due to a mutation leading to a
substantial reduction of the feedback inhibition normally exerted in a
wild-type (P2) plant by Pro at the level of the
-pyrroline-5-carboxylate synthetase enzyme.
1
N.H.R. is a recipient of a Fonds pour la
Recherche dans l'Industrie et dans l'Agriculture fellowship
from the Fond National de la Recherche Scientifique Belge. This work
was supported by the Belgian "Fonds voor Kollektief Fundamental
Onderzoek" (grant no. 2.0094.94), by the Belgian "Nationale
Loterij" (grant nos. 9.0192.98 and 9.0006.93) and by the Fund for
Scientific Research Flanders (Belgium; grant no. G.0192.98).
*
Corresponding author; e-mail nroosens{at}vub.ac.be; fax
32-2-3590399.
© 1999 American Society of Plant Physiologists