Hot water extract of scallop was treated with actinase E and fractionated b
y Sephadex G-25 gel-filtration and DEAE Sephadex A-25 ion-exchange chromato
graphy. The antitumor activity of these fractions against Meth-A fibrosarco
ma was examined. The nonadsorbed fraction (SCA25A) and weakly adsorbed frac
tion (SCA25B) obtained on DEAE Sephadex A-25 anion-exchange gel showed stro
ng antitumor activity. Chemical analyses and NMR spectra identified SCA25A
and SCA25B as glycogen. However, glycogen extracted from the scallop with t
richloroacetic acid and from abalone showed no antitumor activity. This dif
ference was thought to be due to variations in the fine structure of the gl
ycogen molecule. The fine structure of glycogen was investigated by a seque
ntial enzyme digestion method using P-amylase and pullulanase, while the un
it chain was analyzed by high performance anion exchange chromatography. Th
e results showed that the antitumor active glycogen was highly branched wit
h a shorter chain than glycogens without antitumor activity.