Jun-ichi Kadokawa*, Le Hooi Lee and Kazuya Yamamoto Pages 1345 - 1352 ( 8 )
Herein, the synthesis of 6-deoxygenated α(1→4)-oligoglucans via thermostable α- glucan phosphorylase (from Aquifex aeolicus VF5)-catalyzed enzymatic chain-elongation is reported from a maltotriose primer using a non-native substrate, 6-deoxy-α-D-glucose 1- phosphate. The enzymatic reaction of the two substrates mainly produced a tetrasaccharide with one 6-deoxy-α-D-glucose unit at the non-reducing end, together with a minor pentasaccharide with two 6-deoxy-α-D-glucose units. The enzymatic chain-elongation from the primer in the presence of 6-deoxy-α-D-glucose 1-phosphate and a native substrate, α-D-glucose 1- phosphate, afforded 6-deoxygenated α(1→4)-oligoglucans with varying degrees of polymerization. This enzymatic chain-elongation catalyzed by thermostable α-glucan phosphorylase is an efficient method to produce non-natural oligosaccharides, that is, 6-deoxygenated α(1→4)- oligoglucans.
6-Deoxygenated α(1→4)-oligoglucan, enzymatic chain-elongation, α-glucan phosphorylase, glycosylation, non-native substrate, maltooligosaccharide primer, non-natural oligosaccharide.
Graduate School of Science and Engineering, Kagoshima University, Kagoshima, Graduate School of Science and Engineering, Kagoshima University, Kagoshima, Graduate School of Science and Engineering, Kagoshima University, Kagoshima