이번 연구에서는 밀배아유의 기능성 향상을 위해 고정화 효소를 이용한 밀배아유의 효소적 에탄올 반응을 수행했고, 효소적 에탄올 반응의 비가압조건과 가압조건을 중점적으로 비교·분석했다. 비가압조건 효소적 에탄올 반응 수행은 밀배아유와 99.9% 에탄올 혼합물에 두 가지 고정화 효소인 Lipozyme TL-IM과 Lipozyme RM-IM를 1~5 w%(밀배아 기준 무게비)로 25 ml 플라스크에 shaking machine 상에서 40~70 ℃, 120 rpm 조건으로 실험을 수행했다. 가압조건상에서의 효소적 에탄올 반응 조건은 고정화 효소 2 w%, 반응 시간 24시간, 반응 온도 40~60 ℃ 및 반응 압력 75, 100, 150, 200 bar으로 수행했다. 실험으로부터 회수된 sample은 트리글리세라이드의 분해 정도를 살펴보기 위해 모노-, 디-, 트리글리세라이드를 HPLC를 이용하여 분석했다. 밀배아유의 전반적인 전환율은 반응온도와 고정화 효소의 농도에 따라 증가했고, 최적 반응 조건은 가압조건 50 ℃, 100 bar이었다.

Enzymatic ethanolysis of wheat germ oil with immobilized lipase was investigated for enhancing the function of wheat germ oil. Ethanolysis reactions were carried out in two different systems; non-pressurized and pressurized system. In non-pressurized system, the enzymatic ethanolysis was carried out in an erlenmeyer flask(25 ml) containing a mixture of wheat germ oil and 99.90% ethanol using 1~5 wt% immobilized lipase as Lipozyme TL-IM and Lipozyme_x000D_ RM-IM and the reaction mixtures were incubated at 40~70 ℃ with 120 rpm shaking. In pressurized system, the enzymatic ethanolysis was carried out at various condition; immobilized lipase concentration(2 wt%), reaction time(24 h), reaction temperature(40~60 ℃) and reaction pressure(75, 100, 150, 200 bars). The samples obtained from each fraction were analyzed by HPLC for analysing contents of monoglyceride, diglyceride, and triglyceride. The conversion of_x000D_ wheat germ oil relied on the reaction temperature and the concentration of immobilized lipase. The optimum condition of enzymatic ethanolysis in non-pressurized and pressurized systems was at 50 ℃ and 100 bar.

Wheat Germ Oil Supercritical Carbon Dioxide Immobilized Lipase Enzymatic Ethanolysis Monoglyceride Diglyceride Triglyceride HPLC

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