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Synthesis of eicosapentaenoyl phosphatidylcholines by polyethylene glycol-modified lipase in benzene
Authors:Takayuki Yoshimoto  Masahide Nakata  Shigehiko Yamaguchi  Tadashi Funada  Yuji Saito  Yuji Inada
Affiliation:(1) Laboratory of Biological Chemistry, Tokyo Institute of Technology, Ookayama, Meguroku, Tokyo 152, Japan
Abstract:Summary Lipase fromCandida cylindracea was modified with activated polyethylene glycol, which was synthesized from agr-carboxymethyl-ohgr-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.
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