A protocol for quick regeneration of a large number of plantlets of Ar
temisia annus (source of a potent antimalarial drug) is being reported
. Multiple shoots were obtained in large numbers from juvenile as well
as vegetative parts of mature plant on Murashige and Skoog's medium (
MS) having 3% sucrose and 800 CIM myoinositol and supplemented with NA
A (0.5 mu M) + BAP (13.0 mu M) + GA(3) (0.3 mu M) + AsP (300.0 mu M) Glu (700.0 mu M) + Arg (300.0 mu M) + Cys - HCl (30.0 mu M). Reversal
of reproductive to vegetative phase and back to reproductive phase co
uld be achieved in the cultured flower buds. The shoots obtained on th
e above medium could be induced to flower. In addition, new shoots tha
t differentiated from vegetative parts of juvenile and mature explants
also produced flowers when cultured on MS with GA(3) (0.3 mu M). Sinc
e artemisinin estimation is correlative to flowering, our results woul
d facilitate better understanding of biosynthesis of this drug in vitr
o.