The disaccharide sucrose (α-d-glucopyranosyl-1,2-β-d-fructofuranoside) is a highly efficient donor substrate for enzymatic glucosylation reactions. A large number of commercially relevant glucosides are produced via this general route. Every sucrose-based glucosylation involves co-production of d-fructose in amounts corresponding to the target glucoside. A separation technology for selective removal, and efficient recovery, of the d-fructose co-product would be highly desirable as a generic platform for downstream process development. Here, we demonstrate organoboronate-complex reactive extraction of d-fructose into an 1-octanol/hexane (4/1, v/v) solvent using methyltrioctyl ammonium chloride as phase transfer catalyst and extractant. We show separation of the d-fructose co-product (100 mM) from equimolar mixture with 2-α-d-glucosyl-glycerol, a cosmetic ingredient that is manufactured industrially from sucrose and glycerol using sucrose phosphorylase. With the main parameters of extraction, stripping and organic phase recycling identified and their effect on product/co-product yield and purity characterized, we developed a three-step extraction process with alternating extraction and stripping stages that removed the d-fructose efficiently at 50 ml operating scale. 2-α-d-glucosyl-glycerol and d-fructose were cleanly separated and obtained in excellent purity (≥90%) at a recovery of 90% and 83%, respectively. Reactive extraction appears to be faster and more selective and resource-efficient than applicable alternatives for separation, including chromatography and membrane nanofiltration. Thus, the established extraction process is promising for industrial application. It could be generically useful to separate d-fructose from glucosides.
|Number of pages||10|
|Publication status||Published - 7 Aug 2020|
ASJC Scopus subject areas
- Environmental Chemistry