4.3 Article

Preparation of Highly Purified Stearidonic Acid from Echium Oil via an Enzymatic Method Combined with Preparative High Performance Liquid Chromatography

期刊

JOURNAL OF OLEO SCIENCE
卷 64, 期 7, 页码 729-736

出版社

JAPAN OIL CHEMISTS SOC
DOI: 10.5650/jos.ess14252

关键词

echium oil; enzymatic method; packed-bed reactor; stearidonic acid

资金

  1. National Research Foundation of Korea (NRF) - Ministry of Education, Science, and Technology [2013R1A1A2006050]
  2. project titled 'Development of rapid detection system for foodborne pathogens to strengthen the food safety and to promote the sea foods consumption' - Ministry of Oceans and Fisheries Korea [20130281]
  3. National Research Foundation of Korea [2013R1A1A2006050] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Stearidonic acid (SDA), an n-3 polyunsaturated fatty acid (PUFA), can be obtained from plant origin oils and it can be a good source of PUFA for vegetarians. SDA can be easily converted to longer PUFA such as docosahexaenoic acid and eicosapentaenoic acid. Highly purified stearidonic acid (SDA) was prepared successfully from echium oil via an enzymatic method combined with preparative high performance liquid chromatography. In the 1st step, SDA enrichment was accomplished using Candida rugosa lipase and 39.5% of SDA was obtained in the fatty acid fraction. Subsequently, the 1st reaction mixture was used for the 2nd enzymatic esterification without any separation process. The 2nd esterification was conducted for further SDA enrichment in a packed-bed reactor using Lipozyme RM IM from Rhizomucor miehei and the SDA content increased in a very short residence time. Ethanol was selected as an appropriate alcohol to react as an acyl receptor, and the other conditions for SDA enrichment were optimized at 20 degrees C of temperature, and 1:4 of molar ratio (i.e., fatty acid to ethanol). Under these conditions, 51.6% of SDA was obtained in the fatty acid fraction after a residence time of 15 min. Finally, highly purified SDA (purity, >99%) was obtained by prep-HPLC using the SDA-rich fraction obtained from the two-step lipase-catalyzed esterification.

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