Biotechnology Letters

, Volume 8, Issue 11, pp 771–776

Synthesis of eicosapentaenoyl phosphatidylcholines by polyethylene glycol-modified lipase in benzene

Authors

  • Takayuki Yoshimoto
    • Laboratory of Biological ChemistryTokyo Institute of Technology
  • Masahide Nakata
    • Laboratory of Biological ChemistryTokyo Institute of Technology
  • Shigehiko Yamaguchi
    • Laboratory of Biological ChemistryTokyo Institute of Technology
  • Tadashi Funada
    • Laboratory of Biological ChemistryTokyo Institute of Technology
  • Yuji Saito
    • Laboratory of Biological ChemistryTokyo Institute of Technology
  • Yuji Inada
    • Laboratory of Biological ChemistryTokyo Institute of Technology
Article

DOI: 10.1007/BF01020820

Cite this article as:
Yoshimoto, T., Nakata, M., Yamaguchi, S. et al. Biotechnol Lett (1986) 8: 771. doi:10.1007/BF01020820

Summary

Lipase fromCandida cylindracea was modified with activated polyethylene glycol, which was synthesized from α-carboxymethyl-ω-methoxypoly-(oxyethylene) and N-hydroxysuccinimide with dicyclohexylcarbodiimide. The modified lipase was soluble in organic solvents such as benzene and catalyzed the reaction of ester-exchange to synthesize eicosapentaenoyl phosphatidylcholines from dipalmitoyl phosphatidylcholine and eicosapentaenoic acid. Either one of palmitic acid at C-1 or C-2 position of the phosphatidylcholine was exchanged with eicosapentaenoic acid.

Copyright information

© Science and Technology Letters 1986