Development of efficient methods for plant regeneration from callus br
oadens the opportunities for genetic manipulation of new turfgrass sel
ections through tissue culture. This study was conducted to induce cal
lus formation and plant regeneration from embryo explants of St. Augus
tinegrass [Stenotaphrum secundatum (Walt.) Kuntze 'Texas Common']. Imm
ature embryo explants incubated in the dark produced yellow, amorphous
callus on Murashige and Skoog (MS) agar-solidified medium with 30 g L
(-1) sucrose and 1 or 5 mg L(-1) dichlo rophenoxyacetic acid (2,4 D).
Subculture to medium with 0.25 mg L(-1) 2,4-D and 0.5 mg L(-1) kinetin
and introduction of a 14-h photoperiod under fluorescent lamps (16 mu
mol m(-2) s(-1) photosynthetic photon flux [PPF]) induced formation o
f white, friable, embryogenic callus. Scanning electronic microscopy r
evealed that plants regenerated via somatic embryogenesis. Complete pl
ant regeneration was achieved from 33% of the original explants after
transfer to 0.5 x MS medium without growth regulators. These rooted pl
antlets were transplanted to a soil mix in the glasshouse with 100% ac
climation success. This system for efficient regeneration of St. Augus
tinegrass from callus could be applied to improved cultivar selection
after environmental stress testing at the cell level.