Following our previously described Agrobacterium tumefaciens-mediated
transformation procedure for Artemisia annua L., we have undertaken se
veral additional experiments to establish the importance of some param
eters such as explant type, age of explant source, A. tumefaciens stra
in and type of binary vector. Several binary vectors were useful for t
he production of transgenic callus on explants of different ages. In t
ransformed calli, a good correlation between integration and expressio
n of foreign DNA was observed: different assays showed expression of b
eta-Glucuronidase, neomycin phosphotransferase II, superoxide dismutas
e and bleomycin acetyl transferase. The regeneration of transgenic pla
nts required more restricted conditions. Only with the pTJK136 Vector
could transgenic plants be obtained from leaf and stem explants from 1
2- to 18-week-old plants. Go-cultivation for 48 h seemed favorable for
the regeneration of transgenic plants. Stable integration and express
ion of the transgenes was also shown in the progeny.