A reliable and standard method was established for micropropagation of
the A70-34 selected genotype of lucerne (Medicago sativa L., genotype
A70-34), aimed at reducing contamination problems, seasonal and pheno
logical influences on regeneration and phytosanitary problems of the m
other plants, while maintaining the regenerative potential for somatic
embryogenesis of the plant tissues. Mother plants were routinely main
tained for several subcultures and somatic embryogenesis was regularly
obtained from the subcultured explants. Proliferation, rooting and em
bryogenetic ability of plants cultured for 30 days was greater than th
ose cultured for 20 days. The regenerative potential of tissues from d
ifferent organs and of triturated and intact whole plants was also tes
ted. Petioles were confirmed as the best source for embryogenesis as f
ar as efficiency and repeatability were concerned, even though regener
ation from other explant types was also achieved. Production of somati
c embryos through mechanical trituration of the in vitro cultured plan
ts was obtained; the regeneration ability of the triturated plants was
greater than that observed in the intact plants.