Cell suspension cultures of buffelgrass were established from two type
s of callus, a friable tan callus and a brown gelatinous callus, using
Murashige and Skoog medium containing 13.6 muM 2,4-dichlorophenoxyace
tic acid (2,4-D). The friable callus formed a rapidly growing suspensi
on culture, designated BG, which had a doubling time of 2.5 days. The
gelatinous callus formed a very slow-growing suspension culture, desig
nated BGG, which had a doubling time of 1 mo. During growth, the mediu
m of the BGG line slowly increased in viscosity, becoming a thickened
gel by the end of the subculture period. Both lines had high cell viab
ility. Embryogenesis could be induced in both lines by culturing on ch
arcoal-containing, 2,4-D-free medium. No embryos formed in the absence
of charcoal.