| Literature DB >> 27283670 |
Jin-A Ko1, Seung-Hee Nam2, Ji-Young Park3, YongJung Wee4, Doman Kim5, Woo Song Lee6, Young Bae Ryu7, Young-Min Kim8.
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.Entities:
Keywords: Dextransucrase; Leuconostoc citreum; Rebaudioside A; Stevioside
Mesh:
Substances:
Year: 2016 PMID: 27283670 DOI: 10.1016/j.foodchem.2016.05.046
Source DB: PubMed Journal: Food Chem ISSN: 0308-8146 Impact factor: 7.514