Synthesis and characterization of glucosyl stevioside using Leuconostoc dextransucrase

Food Chem. 2016 Nov 15:211:577-82. doi: 10.1016/j.foodchem.2016.05.046. Epub 2016 May 9.

Abstract

Glucosyl stevioside was synthesized via transglucosylation by dextransucrase from Leuconostoc citreum KM20 (LcDexT), forming α-d-glucosyl stevioside. A production yield of 94% was reached after 5days of LcDexT reaction at 30°C. Glucosyl stevioside induced a 2-fold improved quality of taste and sweetness, compared to stevioside. After 15days of storage at 25°C, 98% of glucosyl stevioside in an aqueous solution was present in a soluble form, compared to only 11% for stevioside or rebaudioside A. Furthermore, glucosyl stevioside exhibited a similar or improved stability in commercially available soft drinks, when compared to stevioside and rebaudioside A. These results suggest that glucosyl stevioside could serve as a highly pure and stable sweetener in soft drinks.

Keywords: Dextransucrase; Leuconostoc citreum; Rebaudioside A; Stevioside.

MeSH terms

  • Carbonated Beverages*
  • Diterpenes, Kaurane / chemical synthesis*
  • Food Additives / chemical synthesis
  • Glucosides / chemical synthesis*
  • Glucosyltransferases / chemical synthesis*
  • Glucosyltransferases / isolation & purification
  • Humans
  • Leuconostoc / enzymology*
  • Sweetening Agents / chemical synthesis*
  • Taste Perception* / physiology

Substances

  • Diterpenes, Kaurane
  • Food Additives
  • Glucosides
  • Sweetening Agents
  • stevioside
  • Glucosyltransferases
  • dextransucrase