Nakao_2008_J.Oleo.Sci_57_371

Reference

Title : Enzymatic synthesis of astaxanthin n-octanoic acid esters - Nakao_2008_J.Oleo.Sci_57_371
Author(s) : Nakao M , Sumida M , Katano K , Fukami H
Ref : J Oleo Sci , 57 :371 , 2008
Abstract :

We examined the enzymatic synthesis of astaxanthin n-octanoic acid esters. Carriers for the immobilized enzyme and reaction conditions such as water content, reaction temperature, and time were examined using Candida cylindracea lipase (Lipase OF). Lipase OF) immobilized by a hydrophobic anion exchange resin (10% w/w content of lipase) gave the best yield in the esterification reaction of astaxanthin. Two milligrams of astaxanthin per 750 microL tri-n-octanoin (ca. 0.3%) was optimum because of the low solubility of tri-n-octanoin. The esters were obtained in a yield of 36.4% under the optimal reaction conditions.

PubMedSearch : Nakao_2008_J.Oleo.Sci_57_371
PubMedID: 18536505

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Citations formats

Nakao M, Sumida M, Katano K, Fukami H (2008)
Enzymatic synthesis of astaxanthin n-octanoic acid esters
J Oleo Sci 57 :371

Nakao M, Sumida M, Katano K, Fukami H (2008)
J Oleo Sci 57 :371