African Journal of
Biotechnology

  • Abbreviation: Afr. J. Biotechnol.
  • Language: English
  • ISSN: 1684-5315
  • DOI: 10.5897/AJB
  • Start Year: 2002
  • Published Articles: 12481

Full Length Research Paper

High regioselective acetylation of vitamin A precursors using lipase B from Candida antarctica in organic media

Jingpeng Sun, Keju Jing* and Yinghua Lu
Department of Chemical and Biochemical Engineering, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, P. R. China.
Email: [email protected]

  •  Accepted: 01 July 2011
  •  Published: 26 September 2011

Abstract

 

The effect of different reaction parameters was explored on the acylation of primary hydroxyl group of 1,6-diol by lipase B from Candida antarctica catalysis in organic solvent. First, the effect of the organic solvents was investigated, and the highest conversion rate was obtained in n-hexane. Then, the effect of the acyl donor was studied. Among several reactants, including acetic acid and two different acetates, vinyl acetate gave the best yield. A maximum monoester yield of 98.5% was obtained using vinyl acetate as acyl donor in n-hexane at 50°C. The substrate concentration was 25 mmol/L, while the diol to vinyl acetate molar ratio was 1:3. Substrate concentration had to be limited due to an inhibitory effect on enzyme by the diol that caused a decrease on initial reaction rate. To promote initial reaction rate, excess vinyl acetate was used. Under the optimum conditions, the conversion rate and mono-acylation selectivity were 98.5 and 100%, respectively. The produced monoester was 6.1 mg/ml, and this amount can be further optimized base on the results presented here.

 

Key word: Acetylation, regioselectivity, immobilized lipase B, biocatalytic processes, vitamin A precursors.