Skip to main content
Log in

Synthesis of vitamin E succinate from Candida rugosa lipase in organic medium

  • Articles
  • Published:
Chemical Research in Chinese Universities Aims and scope

Abstract

A screening of commercially available lipases for the synthesis of vitamin E succinate showed that lipase from Candida rugosa presented the highest yield. The synthesis of vitamin E succinate in organic solvents with different lgP values ranging from −1.3 to 3.5 was investigated. Of particular interest was that dimethyl sulfoxide (DMSO) with the lowest lgP exhibited the highest yield among all the organic solvents used. It suggests that lgP is incapable of satisfactorily predicting the biocompatibility of organic solvents due to the complexity of enzymatic reaction with hydrophilic and hydrophobic substrates in organic solvent. Effects of different operating conditions, such as molar ratio of substrate, enzyme concentration, reaction temperature, mass transfer, and reaction time were also studied. Under the optimum conditions of 10 g/L enzyme, a stirring rate of 100 r/min, a substrate molar ratio of 5:1 at 55 °C for 18 h, a satisfactory yield(46.95%) was obtained. The developed method has a potential to be used for efficient enzymatic production of vitamin E succinate.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Valentin H. E., Qi Q., Appl. Microbiol. Biotechnol., 2005, 68, 436

    Article  CAS  Google Scholar 

  2. Barros L., Correia D. M., Ferreira I. C. F. R., Baptistaa P., Santos-Buelga C., Food Chem., 2008, 110, 1046

    Article  CAS  Google Scholar 

  3. Israel K., Yu W., Sanders B. G., Kline K., Nutrition Cancer, 2000, 36, 90

    Article  CAS  Google Scholar 

  4. Quin J., Engle D., Litwiller A., Peralta E., Grasch A., Boley T., Hazelrigg S., J. Surgical Res., 2005, 127, 139

    Article  CAS  Google Scholar 

  5. Prasad K. N., Kumar B., Yan X. D., Hanson A. J., Cole W. C., J. Am. Coll. Nutrition, 2003, 22, 108

    Article  CAS  Google Scholar 

  6. Bonrath W., Cirillo F., Process for the Preparation of Tocol Acylates and Tocopherol Acylates, US6444098B2, 2002

  7. Torres P., Reyes D. D., Lopez C. N., Ferrer M., Ballesteros A., Plou F. J., Process Biochem., 2008, 43, 145

    Article  CAS  Google Scholar 

  8. Xin J., Chen L., Zhang Y., Wen R. R., Zhao D. M., Xia C. G., Food Biotechnol., 2011, 25, 43

    Article  CAS  Google Scholar 

  9. Yin C. H., Zhang C., Gao M., Chinese. J. Chem. Eng., 2011, 19, 135

    Article  CAS  Google Scholar 

  10. Castillo E., Pezzotti F., Navarro A., López-Munguía A., J. Biotechnol., 2003, 102, 251

    Article  CAS  Google Scholar 

  11. Kaewprapan K., Tuchinda P., Marie E., Durandc A., Inprakhon P., J. Mol. Catal. B: Enzymatic, 2007, 47, 135

    Article  CAS  Google Scholar 

  12. Ferreira L., Gil M. H., Cabrita A., Dordick J. S., Biomaterials, 2005, 26, 4707

    Article  CAS  Google Scholar 

  13. Ferreira L., Gil M. H., Dordick J. S., Biomaterials, 2002, 23, 3957

    Article  CAS  Google Scholar 

  14. Laane C., Boeren S., Vos K., Veeger C., Biotechnol. Bioeng., 1987, 30, 81

    Article  CAS  Google Scholar 

  15. Klibanov A. M., Nature, 2001, 409, 241

    Article  CAS  Google Scholar 

  16. Carrea G., Riva S., Angew. Chem. Int. Ed., 2000, 39, 2226

    Article  CAS  Google Scholar 

  17. Klibanov A. M., Acc. Chem. Res., 1990, 23, 114

    Article  CAS  Google Scholar 

  18. Rubio E., Fernandez M. A., Klibanov A. M., J. Am. Chem. Soc., 1991, 113, 695

    Article  CAS  Google Scholar 

  19. Gogoi P., Hazarika S., Dutta N. N., Rao P. G., Chem. Eng. J., 2009, 155, 810

    Article  CAS  Google Scholar 

  20. Hazarika S., Goswami P., Dutta N. N., Chem. Eng. J., 2003, 94, 1

    Article  CAS  Google Scholar 

  21. Lu J. K., Nie K. L., Wang F., Tan T. W., Bioresour. Technol., 2008, 99, 6070

    Article  CAS  Google Scholar 

  22. Yang T., Rebsdorf M., Engelrud U., Xu X., J. Food Lipids, 2005, 12, 299

    Article  CAS  Google Scholar 

  23. Duan Z. Q., Du W., Liu D. H., Process Biochem., 2010, 45, 1923

    Article  CAS  Google Scholar 

  24. Wolff A., Zhu L., Wong Y., Straathof A., Jongejan J., Heijnen J., Biotechnol. Bioeng., 1999, 62, 125

    Article  CAS  Google Scholar 

  25. Han S. Y., Pan Z. Y., Huang D. F., Ueda M., Wang X. N., J. Mol. Catal. B: Enzymatic, 2009, 59, 16

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to He Huang.

Additional information

Supported by the National High-Tech Research and Development Program of China(No.2011AA02A209), the Key Project of National Natural Science Foundation of China(No.20936002) and the National Natural Science Foundation of China for Young Scholars(No.20906049).

Rights and permissions

Reprints and permissions

About this article

Cite this article

Jiang, Xj., Hu, Y., Jiang, L. et al. Synthesis of vitamin E succinate from Candida rugosa lipase in organic medium. Chem. Res. Chin. Univ. 29, 223–226 (2013). https://doi.org/10.1007/s40242-013-2486-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40242-013-2486-z

Keywords

Navigation