Purification of stearidonic acid (18:4(n-3)) and hexadecatetraenoic acid (16:4(n-3)) from algal fatty acid with lipase and medium pressure liquid chromatography
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作者:
Ishihara, K
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机构:Natl Res Inst Fisheries Sci, Marine Biochem Div, Kanazawa Ku, Yokohama, Kanagawa 2368648, Japan
Ishihara, K
Murata, M
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机构:Natl Res Inst Fisheries Sci, Marine Biochem Div, Kanazawa Ku, Yokohama, Kanagawa 2368648, Japan
Murata, M
Kaneniwa, M
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机构:Natl Res Inst Fisheries Sci, Marine Biochem Div, Kanazawa Ku, Yokohama, Kanagawa 2368648, Japan
Kaneniwa, M
Saito, H
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机构:Natl Res Inst Fisheries Sci, Marine Biochem Div, Kanazawa Ku, Yokohama, Kanagawa 2368648, Japan
Saito, H
Komatsu, W
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机构:Natl Res Inst Fisheries Sci, Marine Biochem Div, Kanazawa Ku, Yokohama, Kanagawa 2368648, Japan
Komatsu, W
Shinohara, K
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机构:Natl Res Inst Fisheries Sci, Marine Biochem Div, Kanazawa Ku, Yokohama, Kanagawa 2368648, Japan
Shinohara, K
机构:
[1] Natl Res Inst Fisheries Sci, Marine Biochem Div, Kanazawa Ku, Yokohama, Kanagawa 2368648, Japan
[2] Toita Womens Coll, Dept Life Sci, Hachioji, Tokyo 1930802, Japan
[3] Natl Food Res Inst, Tsukuba, Ibaraki 3050856, Japan
Stearidonic acid (18:4(n-3)) and hexadecatetraenoic acid (16:4(n-3)) are included in some edible marine algae such as Undaria pinnatifida and Ulva pertusa with relatively high compositions (up to 40%) of total fatty acids. In order to prepare 16:4(n-3) and 18:4(n-3) enriched fatty acid concentrates, we screened for a suitable lipase which concentrates these acids by the removal of other fatty acids in the selective esterification reaction reported by Shimada er al. (Shimada et al. (1997), J. Am. Oil Chem. Sec., 74, 1465-1470). In combination with the lipase reaction and reversed-phase medium pressure liquid chromatography, Ne purified 18:4(n-3) and 16:4(n-3) to more than 95% purity.