Ginger anthers collected at the uninucleate microspore stage were subjected
to a cold treatment (0 degrees) for 7 d and induced to develop profuse cal
lus on MS medium supplemented with 2-3 mg l(-1) 2, 4-D. Plantlets could be
regenerated from these calli on MS medium supplemented with 5-10 mg l(-1) B
AP and 0.2 mg l(-1) 2,4-D. The regenerated plantlets could be established i
n soil with 85% success, when they were planted in potting mixture of garde
n soil, sand and vermiculite in equal proportions and kept in a humid chamb
er initially for 22-30 d. This is the first report of successful regenerati
on of plants from ginger anther cultures and the protocol can be used for p
ossible development of androgenic haploids and dihaploids in ginger.