Abstract
A method has been developed for the regeneration of transformed plants of the commercially important crop sugarbeet (Beta vulgaris L.), using Agrobacterium tumefaciens. Binary vectors were used, carrying both screenable and selectable genes. Plant regeneration from shoot-base tissues was found to be relatively rapid and frequent compared with petioles or leaf tissue. Inoculation of cultured shoot-base tissues resulted in the production of transformed plants, as determined by (1) introduced resistance to kanamycin, (2) introduced CAT or GUS activity, and (3) Southern blot analysis to show the integration of foreign DNA. The transformation frequency was found to be dependent upon explant source, plant genotype and selection conditions used.