Genetic transformation of peppermint is known to be very difficult ess
entially because of low efficiency regeneration. A regeneration protoc
ol allowing 51% shooting frequency is proposed. Transient beta-glucuro
nidase expression and adjustment of selection pressure with kanamycin
are also reported. The final retained method to attempt peppermint tra
nsformation is: Agrobacterium inoculation or biolistic treatment of th
e first apical leaves of in vitro clones, regeneration in the dark wit
h kanamycin (1 mg l(-1)) and 6-benzylaminopurine (2 mg l(-1)), followe
d by selection of regenerated shoots with 200 mg l(-1) kanamycin.