Skip to main content
Log in

Enzymatic Synthesis of Lipophilic Caffeoyl Lipids Using Soybean Oil as the Novel Acceptor

  • Research Paper
  • Published:
Biotechnology and Bioprocess Engineering Aims and scope Submit manuscript

Abstract

Soybean oil-based caffeoyl lipids are the novel lipophilic derivatives of caffeic acid, which can be used as UV absorbers and antioxidants in the food and cosmetic industries. In the work, the novel lipophilic structured lipids were prepared using soybean oil as the novel caffeoyl acceptor by enzymatic transesterification. The effects of the reaction variables on the transesterification were investigated, and response surface methodology was used to optimize the reaction variables. Reactions were monitored by HPLC-UV. Different enzymes (Novozym 435, Lipozyme RMIM, and Lipozyme TLIM) were used as biocatalysts, and Novozym 435 showed the best performance for the reaction. The results showed that a high lipophilic soybean oil-based caffeoyl lipids yield (73.5 ± 1.2%) was achieved under the optimal conditions (reaction temperature 85°C, substrate molar ratio 1:6 (ethyl caffeate (EC)/soybean oil), enzyme load 25% (w/w), and 60 h at atmosphere pressure). The activation energies of EC conversion, hydrophilic glyceryl caffeates (GC) and lipophilic caffeoylated acylglycerol (CAG) formations were 32.92 kJ/mol, 17.21 kJ/mol and 57.36 kJ/mol, respectively. Km and Vm were 0.022 mol/L and 0.033 × 10-3 mol/(Lmin), respectively.

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. Bakalbassis, E. G., N. Nenadis, and M. Tsimidou (2003) A density functional theory study of structure-activity relationships in caffeic and dihydrocaffeic acids and related monophenols. J. Am. Oil Chem. Soc. 80: 459–466.

    Article  CAS  Google Scholar 

  2. Deshmukh, R., M. Kaundal, V. Bansal, and Samardeep (2016) Caffeic acid attenuates oxidative stress, learning and memory deficit in intra-cerebroventricular streptozotocin induced experimental dementia in rats. Biomed. Pharmacother. 81: 56–62.

    Article  CAS  PubMed  Google Scholar 

  3. Gülçin, I. (2006) Antioxidant activity of caffeic acid (3,4-dihydroxycinnamic acid). Toxicology 217: 213–220.

    Article  CAS  PubMed  Google Scholar 

  4. Moosavi, F., R. Hosseini, H. Rajaian, T. Silva, D. M. Silva, L. Saso, N. Edraki, R. Miri, F. Borges, and O. Firuzi (2017) Derivatives of caffeic acid, a natural antioxidant, as the basis for the discovery of novel nonpeptidic neurotrophic agents. Bioorgan. Med. Chem. 25: 3235–3246.

    Article  CAS  Google Scholar 

  5. Prasad, N. R., K. Jeyanthimala, and S. Ramachandran (2009) Caffeic acid modulates ultraviolet radiation-B induced oxidative damage in human blood lymphocytes. J. Photoch. Photobio. B 95: 196–203.

    Article  CAS  Google Scholar 

  6. Wu, Z., Z. Yu, Z. Cui, L. Peng, H. Li, C. Zhang, H. Shen, P. Yi, and B. Fu (2017) In vitro antiviral efficacy of caffeic acid against canine distemper virus. Microb. Pathogenesis 110: 240–244.

    Article  CAS  Google Scholar 

  7. Li, X., Z. Yan, L. Pan, H. Jin, X. Yang, J. Liu, X. He, X. Ren, M. Xie, K. Guo, and B. Qin (2017) Caffeic acid derivatives as growth inhibitors of Setaria viridis: structure-activity relationships and mechanisms. Phytochem. Lett. 20: 208–213.

    Article  CAS  Google Scholar 

  8. Chen, H., Y. Twu, C. Chang, Y. Liu, and C. Shieh (2010) Optimized synthesis of lipase-catalyzed octyl caffeate by Novozym 435. Ind. Crop. Prod. 32: 522–526.

    Article  CAS  Google Scholar 

  9. Sorensen, A. D. M., E. Durand, M. Laguerre, C. BayrasyM, J. Lecomte, P. Villeneuve, and C. Jacobsen (2014) Antioxidant properties and efficacies of synthesized alkyl caffeates, ferulates and coumarates. J. Agr. Food Chem. 62: 12553–12562.

    Article  CAS  Google Scholar 

  10. Yang, Y., T. Raku, E. Song, S. Park, D. Yoo, H. Park, B. Kim, H. Kim, S. Lee, H. Kim, and Y. Tokiwa (2012) Lipase catalyzed reaction of L-ascorbic acid with cinnamic acid esters and substituted cinnamic acids. Biotechnol. Bioprocess Eng. 17: 50–54.

    Article  CAS  Google Scholar 

  11. Kumar, V., F. Jahan, S. Raghuwanshi, R. V. Mahajan, and R. K. Saxena (2013) Immobilization of Rhizopus oryzae lipase on magnetic Fe3O4-chitosan beads and its potential in phenolic acids ester synthesis. Biotechnol. Bioprocess Eng. 18: 787–795.

    Article  CAS  Google Scholar 

  12. Yang, Z., Z. Guo, and X. Xu (2012) Ionic liquid-assisted solubilization for improved enzymatic esterification of phenolic acids. J. Am. Oil Chem. Soc. 89: 1049–1055.

    Article  CAS  Google Scholar 

  13. Chen, H., J. Chen, C. Chang, and C. Shieh (2011) Optimization of ultrasound-accelerated synthesis of enzymatic caffeic acid phenethyl ester by response surface methodology. Ultrason. Sonochem. 18: 455–459.

    Article  CAS  PubMed  Google Scholar 

  14. Tolba, M., H. Omar, S. Azab, A. Khalifa, A. Abdel-Naim, and S. Abdel-Rahman (2014) Caffeic acid phenethyl ester: a review of its antioxidant activity, protective effects against ischemiareperfusion injury and drug adverse reactions. Crit. Rev. Food Sci. 56: 2183–2190.

    Article  CAS  Google Scholar 

  15. Pang, N., S. Gu, J. Wang, S. Cui, F. Wang, X. Liu, X. Zhao, and F. Wu (2013) A novel chemoenzymatic synthesis of propyl caffeate using lipase-catalyzed transesterification in ionic liquid. Bioresour. Technol. 139: 337–342.

    Article  CAS  PubMed  Google Scholar 

  16. Zheng, J., R. Zhang, Y. Chen, X. Ye, Q. Chen, D. Shen, and Q. Wang (2017) Synthesis of caffeic acid ester morpholines and their activation effects on tyrosinase. Process Biochem. 62: 91–98.

    Article  CAS  Google Scholar 

  17. Tan, Z. and F. Shahidi (2012) A novel chemoenzymatic synthesis of phytosteryl caffeates and assessment of their antioxidant activity. Food Chem. 133: 1427–1434.

    Article  CAS  Google Scholar 

  18. Feddern, V., Z. Yang, X. Xu, E. Badiale-furlong, and L. De Souza-Soares (2011) Synthesis of octyl dihydrocaffeate and its transesterification with tricaprylin catalyzed by candida antarctica lipase. Ind. Eng. Chem. Res. 50: 7183–7190.

    Article  CAS  Google Scholar 

  19. Yang, Z., V. Feddern, M. Glasius, Z. Guo, and X. Xu (2011) Improved enzymatic production of phenolated glycerides through alkyl phenolate intermediate. Biotechnol. Lett. 33: 673–679.

    Article  CAS  PubMed  Google Scholar 

  20. Sun, S., P. Wang, and S. Zhu (2017) Enzymatic incorporation of caffeoyl into castor oil to prepare the novel castor oil-based caffeoyl structured lipids. J. Biotechnol. 249: 66–72.

    Article  CAS  PubMed  Google Scholar 

  21. Ha, S., T. Anh, S. Sang, and Y. Koo (2012) Effect of ionic liquids on enzymatic synthesis of caffeic acid phenethyl ester. Bioproc. Biosyst. Eng. 35: 235–240.

    Article  CAS  Google Scholar 

  22. Sun, D. and X. Chen (2015) Kinetics of enzymatic synthesis of monoferuloyl glycerol and diferuloyl glycerol by transesterification in [BMIM]PF6. Biochem. Eng. J. 97: 25–31.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Shangde Sun.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sun, S., Tian, L., Hu, B. et al. Enzymatic Synthesis of Lipophilic Caffeoyl Lipids Using Soybean Oil as the Novel Acceptor. Biotechnol Bioproc E 23, 557–563 (2018). https://doi.org/10.1007/s12257-018-0215-7

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12257-018-0215-7

Keywords

Navigation