1Department of Botany, Faculty of Science, Hamdard University, New Delhi 110 062, India
2Centre for Biotechnology, Faculty of Science, Hamdard University, New Delhi 110 062, India
AbbreviationsNAA
α-naphthaleneacetic acid
BAP6- benzylaminopurine
Ztzeatin
IAAindole-3-acetic acid
Knkinetin
MSMurashige and Skoog's
Regeneration from leaf, shoot apex and nodal segments of in vivo and in vitro seedlings, and enhancement in silybin content have been achieved in Silybum marianum. The explants callused within four weeks on Murashige and Skoog's medium (MS) (1) supplemented with a-naphthaleneacetic acid (NAA, 0.1 mg I−1) + 6-benzylaminopurine (BAP, 0.3 mg I−1) + Zeatin (Zt, 0.3 rng I−1). Upon transfer to MS + NAA (0.1 mg I−1) + Zt (0.5 mg I−1), the callus differentiated multiple shoots followed by rooting in 100% cultures of all the explants within ten weeks. Direct shoot regeneration could be obtained only from nodal segments after 4 weeks on MS + Indoled-acetic acid (IAA, 0.1 mg I−1) + Kinetin (Kn, 0.5 mg I−1) in 100% cultures. Rooting of these shoots was achieved after 2 weeks on MS + NAA (0.1 mg I−1) + Zt (0.5 mg I−1). Plantlets could be successfully transplanted to soil. Yield of silybin content in the cultured tissues varied with age and composition of the medium. Maximum yield resulted after eight weeks on media supplemented with zeatin.
Silybum marianum, medicinal plant, plant regeneration, silybin