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Location: Home>Papers of Journal of Molecular Catalysis
Enzymatic Glycosylation for Synthesis of 4-Hydroxyl Phenylethyl β-D-Glucoside in Medium Containing Ionic Liquids
2011-07-11 ArticleSource:
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YUE Lei1, LIN Qiong-Mei1, XU Ge1, LIN Lei 1, SHI Xian-Ai1,2*

 (1. College of Biological Science and Engineering, Fuzhou University, Fuzhou, Fujian 350108, China 2. Fujian Key Laboratory of Medical Instrument and Pharmaceutical Technology, Fuzhou, Fujian 350002, China)

Abstract: The glycosylation catalyzed by β-glucosidase for synthesis of 4-hydroxyl phenylethyl β-D-glucoside (salidroside) in mixed medium of ionic liquids/organic solvent/buffer solution was studied. The effects of some important factors on the glycosylation such as the constitution of the medium, and the reaction conditions were investigated. The results showed that 1-butyl-3-methylimidazolium hexafluorophosphate (C4MIm·PF6) /1,4-dioxane/citric acid-phosphate buffer was the proper mixed medium for biosynthesis of salidroside. When the volume proportions of these components were 17%, 68% and 15% respectively, the product concentration would reach 18.9 mg/mL under these conditions: D-(+)-glucose 100 mg/mL, 4-hydroxyphenethyl alcohol (tyrosol) 220 mg/mL, β-glucosidase 12 U/mL, pH 6.0, 50 ℃ and 275 rpm for 120 h.

Key words: β-Glucosidase; salidroside; ionic liquid; glycosylation

E-mail: shixa@fzu.edu.cn

Journal of Molecular Catalysis, Vol. 25, Issue 3, 2011, 269~275

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