Hypocotyls, cotyledons and etiolated half-expanded leaves of Cucumis m
elo 'Green Delica' were used as explants for protoplast isolation and
culture. Protoplasts isolated from cotyledons and etiolated half-expan
ded leaves cultured in Durand, Potrykus and Donn (DPD) medium suppleme
nted with 0.9 mu M benzylaminopurine (BAP), 3.6 mu M 2,4-dichloropheno
xyacetic acid (2,4-D) and 1% sucrose, using the agarose bead culture m
ethod, were able to form cell walls and subsequently go through cell d
ivision. Pretreatment of half-expanded leaf explants in the dark for 1
4 d provided the best material for protoplast isolation and cell divis
ion. Approximately one third of protoplasts from etiolated half expand
ed leaves formed microcolonies. For hypocotyl protoplasts, none of the
treatments used were suitable to induce cell division. There was no s
ignificant difference between sucrose, glucose, and sucrose plus gluco
se, in culture media on the plating efficiency of leaf protoplasts of
C. melo 'Green Delica'; however, bigger colonies were formed in media
supplemented with 1% sucrose. No shoot or whole plant regeneration was
achieved. However, the methods reported here provide further informat
ion on C. melo protoplast culture. (C) 1998 Annals of Botany Company.