Techniques quantifying [C-14]photoassimilate partitioning between hexo
se and sucrose can identify developmental and regulatory changes in su
gar metabolism of sorghum (Sorghum bicolor (L.) Moench]. The objective
of this study was to develop a laboratory method for separating and q
uantifying [C-14]hexose and [C-14]sucrose in numerous plant organ extr
acts simultaneously. The described method combines easily with availab
le assays for [C-14]starch and [C-14]Structural components and for tot
al fructose, glucose, sucrose, and starch. Treatment with hexokinase i
s followed by batch treatment with anion exchange resin. Hexose, as he
xose phosphate, binds (> 95%) to the resin, and sucrose remains unboun
d (> 95%). Radiolabel in extracts is nearly completely recovered (99%)
. Determinations are reproducible (SE = 1.3%). This method was applied
to identify differences in sugar metabolism between organs and among
growth stages of field-grown sorghum.