The myo-inositol oxidation pathway was investigated in regard to its role as a source of carbon for products of hexose monophosphate metabolism in germinated polen of Lilium longiflorum Thunb., cv. has been noted in other plant tissues including parsley leaves (20), strawberry fruits (20), corn seedlings (9), and lily pistils (12), but processes involved in this conversion have yet to be determined.Biosynthesis of myo-inositol involves direct cyclization of Dglucose-6-P to L-myo-inositol-1-P. Conversion of myo-inositol to glucose by reversal of this reaction would require formation of L-myo-inositol-1-P. Formation of myo-inositol-1-P from myoinositol was found in detached corn root tips by J. Dehusses (see ref. 16) and the kinase for this reaction has been described (7) but conversion of L-myo-inositol-1-P to D-glucose-6-P by reversal of myo-inositol-1-P synthase could not be demonstrated (21).Alternatively, conversion of myo-inositol to glucose could occur after oxidative cleavage of myo-inositol to glucuronate. Indeed, when D_[1-14C]glucurono-6,3-lactone was fed to detached strawberry fruits, significant 14C was recovered in sucrose and xylose (8). Free -xylose was readily converted to sucrose in the strawberry (17). Animals also convert myo-inositol to hexose over a pathway known as the glucuronate-xylulose cycle (25) which involves reduction of D-glucuronic acid to L-gulonic acid. Although plant tissues also reduced D-glucuronate and its lactone to L-gulonic acid (8,18,20), L-gulonic acid merely accumulated. When L-[1-14C]-or L-[6-14C]gulono-1,4-lactone was fed to detached strawberry fruits or bean apices, a portion was hydrolyzed to L-gulonic acid but none of the label was found in polysaccharide fractions (2). It seems unlikely that the glucuronate-xylulose cycle plays a role in the conversion of myo-inositol to hexose in plants.The present paper examines the metabolic fate of specifically labeled carbohydrates peculiar to the myo-inositol oxidation pathway and to -glucuronate metabolism. Results
MATERIALS AND METHODSPollen. Anthers of Lilium longiflorum Thumb., cv. Ace (Easter lily) were collected in a commercial greenhouse on the day of anthesis. Anthers were dried in an open, well ventilated area and shaken on 20-mesh screen to recover the pollen which was stored at 4 C as described earlier (4). Two batches collected in March, 1972 were used in these experiments. Batch A with 50 ± 4% germination was used for uptake studies and batch B with 75 + 5% for isolation of labeled products.Uptake of myo-inositol was delayed by the time required for 89 www.plantphysiol.org on May 9, 2018 -Published by Downloaded from