A biolistic transformation method was developed, for the first time, f
or durum wheat (Triticum turgidum L., 2n = 4x = 28; AABB) cultivar Med
ora using isolated scutella as target cells, gus as a reporter gene, a
nd bar (herbicide resistance gene) as a selectable marker, An average
of 116 GUS foci per scutellum were observed 2 days after bombardment,
After selection for herbicide resistance by adding 5 mg/l L-phosphinot
hricin (L-PPT) to the medium during regeneration and spot application
of 120 mg/l L-PPT on the leaves of regenerated plants, we identified f
ive resistant plants from a total of 245 scutella bombarded, All these
plants were fertile, Of the 1048 T-1 seeds germinated from five lines
(dwt1, dwt2, dwt3, dwt4, and dwt5), a total of 104 T-1 plants were re
covered that showed resistance to the herbicide glufosinate when spray
ed at a concentration of 120 mg/l L-PPT Some of the herbicide-resistan
t T-1 plants exhibited phosphinothricin acetyltransferase (PAT) enzyme
activity, indicating the presence of the bar gene in the transgenics,
The integration of gus and bar genes into the genomes of durum wheat
was further confirmed by Southern analysis, Development of this transf
ormation procedure with an agronomically superior durum cultivar will
open up new avenues for the enhancement of the existing germplasm thro
ugh biotechnology.