Biocatalytic synthesis of 2-O-α-D-glucopyranosyl-L-ascorbic acid using an extracellular expressed α-glucosidase from Oryza sativa

Background 2-O-alpha-D-Glucopyranosyl-L-ascorbic acid (AA-2G) is an important derivative of L-ascorbic acid (L-AA), which has the distinct advantages of non-reducibility, antioxidation, and reproducible decomposition into L-AA and glucose. Enzymatic synthesis is a preferred method for AA-2G production over alternative chemical synthesis owing to the regioselective glycosylation reaction. alpha-Glucosidase, an enzyme classed into O-glycoside hydrolases, might be used in glycosylation reactions to synthesize AA-2G. Main Methods and Major Results Here, an alpha-glucosidase from Oryza sativa was heterologously produced in Pichia pastoris GS115 and used for biosynthesis of AA-2G with few intermediates and byproducts. The extracellular recombinant alpha-glucosidase (rAGL) reached 9.11 U mL-1 after fed-batch cultivation for 102 h in a 5 L fermenter. The specific activity of purified rAGL is 49.83 U mg-1 at 37 degrees C and pH 4.0. The optimal temperature of rAGL was 65 degrees C, and it was stable below 55 degrees C. rAGL was active over the range of pH 3.0-7.0, with the maximal activity at pH 4.0. Under the condition of 37 degrees C, pH 4.0, equimolar maltose and ascorbic acid sodium salt, 8.7 +/- 0.4 g L-1 of AA-2G was synthesized by rAGL. Conclusions and Implications The production of rAGL in P. pastoris was proved to be beneficial in providing enough enzyme and promoting biocatalytic synthesis of AA-2G. These studies lay the basis for the industrial application of alpha-glucosidase.

Automated summary

An alpha-glucosidase from Oryza sativa was heterologously produced in Pichia pastoris and used for the efficient biosynthesis of AA-2G. The purified enzyme displayed high specific activity at 37 degrees C and pH 4.0, and successfully synthesized AA-2G under specific conditions. These studies provide a foundation for the industrial application of alpha-glucosidase.