An in vitro method for the initiation of minibeet development from der
ooted sugarbeet seedlings was developed. The surface sterilized seeds
were germinated for 25 days on sugar-free Murashige and Skoog medium c
ontaining half-strength nutritive elements, 10 mg 1(-1) thiamine, 0.1
mg 1(-1) gibberellic acid and 7.0 g 1(-1) agar. After germination, see
dlings of six different genotypes were derooted at the root neck and i
ncubated for 90-120 days on minibeet initiation medium containing doub
le-strength Murashige and Skoog elements, B-5 vitamins, 100 mg 1(-1) a
ctivated charcoal, 30 g 1(-1) D-glucose, 6-benzylaminopurine (0.2 mg 1
(-1)) and abscisic acid (0.2 mg 1(-1)). Without subculturing, minibeet
s developed on 20-40% of five different genotypes of seedlings. The de
veloped minibeets were characterized structurally and functionally by
means of a histological study and relative sucrose accumulation. Minib
eets were compared to tuber-like formations which showed neither polyc
ambial structure nor relative sucrose accumulation. Minibeets gave ris
e to plants after potting in the greenhouse.