Jun-ichi Kadokawa
Kagoshima University, Kagoshima Japan
Title: Enzyme as useful catalyst for precision synthesis of functional polysaccharide materials
Biography
Biography: Jun-ichi Kadokawa
Abstract
Natural polysaccharides such as cellulose, starch, and chitin are widely distributed in nature and thus considered as the very important biomass resources. They can also be expected as functional materials, which are applicable in biomedical, tissue engineering, and environmentally benign fields. Therefore, the efficient methods for synthesis of functional polysaccharides have attracted much attention to provide new materials employed in such application fields. Enzymatic approaches have increasingly been important to precisely synthesize functional polysaccharide materials. Phosphorylase is one of the enzymes, which have been practically employed as catalysts for the synthesis of polysaccharides with well-defined structures. This enzyme catalyzes enzymatic polymerization of a-d-glucose 1-phosphate (Glc-1-P) as a monomer initiated from the nonreducing end of maltooligosaccharide primer to produce a(1g4)-glucan, that is amylose (Figure 1). The author has reported precision synthesis of functional polysaccharide materials by phosphorylase-catalyzed enzymatic reactions.1,2
By means of the property of spontaneously double helix formation from amyloses, for example, it was reported that the phosphorylase-catalyzed enzymatic polymerization using the immobilized primers forms network structures composed of the double helix cross-linking points.3 In most cases, accordingly, the enzymatic polymerization solutions have turned into hydrogels with high water contents. As an example, the phosphorylase-catalyzed enzymatic polymerization using the immobilized primers on chitin nanofibers was investigated to produce amylose-grafted chitin nanofiber hydrogels.4
On the other hand, the author has also reported that by means of the phosphorylase-catalyzed enzymatic polymerization using analog substrates as monomers, well-defined polysaccharides with functional groups are efficiently obtained.5 For example, phosphorylase isolated from thermophilic bacteria, Aquifex aerolicus VF5, catalyzed the enzymatic polymerization of a-d-glucosamine 1-phosphate (GlcN-1-P) as a monomer from maltotriose primer. The enzymatic reaction was accelerated in ammonia buffer containing Mg2+ ion, owing to the precipitation of inorganic phosphate, giving the high molecular weight aminopolysaccharide, which corresponded to chitosan stereoisomer.
