Culture conditions for sweet potato callus were manipulated to enhance
starch content. Tissue cultures were frozen in liquid nitrogen, pulve
rized in a ceramic mortar, and ground with a buffer and sea sand. Frac
tional centrifugation in a discontinuous Percoll gradient enabled sepa
ration of amyloplasts in a 40% Percoll layer sandwiched between 20% an
d 50% layers. A latency test of marker enzymes for amyloplast, and a p
reliminary feeding experiment with radio-labeled substrates for starch
synthesis confirmed that the preparation is suitable for use in the s
tudy of starch biosynthesis.