Chinese Journal of Catalysis ›› 2011, Vol. 32 ›› Issue (6): 1051-1055.DOI: 10.3724/SP.J.1088.2011.01211

• Research papers • Previous Articles     Next Articles

Biocatalytic Synthesis of Salidroside by β-Glucosidase in Ionic Liquids

WANG Mengliang*, GUO Chunxia   

  1. Institute of Applied Chemistry, Shanxi University, Taiyuan 030006, Shanxi, China
  • Received:2010-12-08 Revised:2011-03-09 Online:2011-06-21 Published:2014-10-31

Abstract: β-Glucosidase modified with polyethylene glycol (PEG) was used as catalyst for the synthesis of salidroside from tyrosol and D-glucose, and its catalytic activity in three ionic liquids, [bmim]PF6, [bmim]BF4, and [bmim]Tf2N, and two common organic solvents, 1,4-dioxane and n-hexane, was measured. Ionic liquid [bmim]PF6 was the optimal reaction medium, and different reaction conditions were optimized in it. A yield of 88.5% (product content of 61.93 mmo1/L) was obtained under the conditions of H2O content of 2%, temperature of 50 oC, tyrosol content of 70 mmo1/L, D-glucose/tyrosol molar ratio of 2, and reaction time of 24 h. The results suggest that both the modification with PEG and using ionic liquid [bmim]PF6 as reaction medium have obvious promoting effects on the enzymatic synthesis of salidroside.

Key words: ionic liquid, β-glucosidase, salidroside, biocatalysis, tyrosol