Fructans are polyfructose molecules that function as nonstructural sto
rage carbohydrates in several plant species that are important crops.
We have been studying plants for their ability to synthesize and degra
de fructans to determine if this ability is advantageous. We have also
been analyzing the ability to synthesize fructan in relation to other
nonstructural carbohydrate storage forms like starch. To study this,
we induced fructan accumulation in normally non-fructan-storing plants
and analyzed the metabolic and physiological properties of such plant
s. The normally non-fructan-storing potato plant was modified by intro
ducing the microbial fructosyltransferase genes so that it could accum
ulate fructans. Constructs were created so that the fructosyltransfera
se genes of either Bacillus subtilis (sacB) or Streptococcus mutans (f
tf) were fused to the vacuolar targeting sequence of the yeast carboxy
peptidase Y (cpy) gene. These constructs were placed under the control
of the constitutive cauliflower mosaic virus 35S promoter and introdu
ced into potato tissue. The regenerated potato plants accumulated high
molecular mass(>5 x 10(6) D) fructan molecules in which the degree of
polymerization of fructose units exceeded 25,000. Fructan accumulatio
n was detected in every plant tissue tested. The fructan content in th
e transgenic potato plants tested varied between 1 and 30% of dry weig
ht in leaves and 1 and 7% of dry weight in microtubers. Total nonstruc
tural neutral carbohydrate content in leaves of soil-grown plants incr
eased dramatically from 7% in the wild type to 35% in transgenic plant
s. Our results demonstrated that potato plants can be manipulated to s
tore a foreign carbohydrate by introducing bacterial fructosyltransfer
ase genes. This modification affected photosynthate partitioning in mi
crotubers and leaves and increased nonstructural carbohydrate content
in leaves.