Enzymatic Modification of Menhaden Oil to Incorporate Caprylic and/or Stearic Acid

Abstract Menhaden oil was enzymatically modified with caprylic (8:0) and/or stearic acid (18:0) to produce structured lipids (SL). The goal was to produce SL with high amounts of polyunsaturated fatty acids (PUFA), a low level of saturation, and a melting point of 25–35 °C. Substrate (menhaden oil t...

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Published in:Journal of the American Oil Chemists' Society
Main Authors: Willett, Sarah A., Martini, Silvana, Akoh, Casimir C.
Other Authors: National Institute of Food and Agriculture
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2019
Subjects:
Online Access:http://dx.doi.org/10.1002/aocs.12227
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spelling crwiley:10.1002/aocs.12227 2024-06-02T07:58:32+00:00 Enzymatic Modification of Menhaden Oil to Incorporate Caprylic and/or Stearic Acid Willett, Sarah A. Martini, Silvana Akoh, Casimir C. National Institute of Food and Agriculture 2019 http://dx.doi.org/10.1002/aocs.12227 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Faocs.12227 https://onlinelibrary.wiley.com/doi/pdf/10.1002/aocs.12227 https://onlinelibrary.wiley.com/doi/full-xml/10.1002/aocs.12227 https://aocs.onlinelibrary.wiley.com/doi/am-pdf/10.1002/aocs.12227 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#am http://onlinelibrary.wiley.com/termsAndConditions#vor Journal of the American Oil Chemists' Society volume 96, issue 7, page 761-775 ISSN 0003-021X 1558-9331 journal-article 2019 crwiley https://doi.org/10.1002/aocs.12227 2024-05-03T10:52:42Z Abstract Menhaden oil was enzymatically modified with caprylic (8:0) and/or stearic acid (18:0) to produce structured lipids (SL). The goal was to produce SL with high amounts of polyunsaturated fatty acids (PUFA), a low level of saturation, and a melting point of 25–35 °C. Substrate (menhaden oil to acyl donor) molar ratios were 1:1, 1:3, and 1:5 for 8:0, and 1:1, 1:2, and 1:3 for 18:0. Enzyme load was 10% of the total weight of substrates. Time course study determined optimal time for maximum acyl donor incorporation. Linear interpolation estimated molar ratios that yielded SL with 20 or 30 mol% incorporation of 8:0 or 18:0. Enzymatic reactions were also conducted with molar ratios of menhaden oil to acyl donors:8:0:18:0 (1:1:3, 1:2:2, and 1:3:1). Lipases from Candida antarctica , Lipozyme® 435, and Rhizomucor miehei , Lipozyme® RM IM (Novozymes North America, Inc., Franklinton, NC, USA), were compared for all reactions. Total and sn ‐2 fatty acid compositions, triacylglycerol (TAG) molecular species, thermal behavior, volatile lipid oxidation products, solid fat contents, and oxidative stability were compared. When 8:0 was the acyl donor, the 1:3.03 and 1:4.58 ratios resulted in incorporation of 20 and 30 mol% 8:0, respectively. With 18:0 as the acyl donor, the 1:1.32 and 1:2.41 ratios led to incorporation of 20 and 30 mol% 18:0, respectively. The 1:3:1 ratio SL had a crystallization onset ( C 0 ) of 15.3 °C and a melting completion ( M c ) of 33.1 °C. The physicochemical properties of these SL suggest that some may be useful in formulating food products such as margarines and spreads. Article in Journal/Newspaper Antarc* Antarctica Wiley Online Library Journal of the American Oil Chemists' Society 96 7 761 775
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description Abstract Menhaden oil was enzymatically modified with caprylic (8:0) and/or stearic acid (18:0) to produce structured lipids (SL). The goal was to produce SL with high amounts of polyunsaturated fatty acids (PUFA), a low level of saturation, and a melting point of 25–35 °C. Substrate (menhaden oil to acyl donor) molar ratios were 1:1, 1:3, and 1:5 for 8:0, and 1:1, 1:2, and 1:3 for 18:0. Enzyme load was 10% of the total weight of substrates. Time course study determined optimal time for maximum acyl donor incorporation. Linear interpolation estimated molar ratios that yielded SL with 20 or 30 mol% incorporation of 8:0 or 18:0. Enzymatic reactions were also conducted with molar ratios of menhaden oil to acyl donors:8:0:18:0 (1:1:3, 1:2:2, and 1:3:1). Lipases from Candida antarctica , Lipozyme® 435, and Rhizomucor miehei , Lipozyme® RM IM (Novozymes North America, Inc., Franklinton, NC, USA), were compared for all reactions. Total and sn ‐2 fatty acid compositions, triacylglycerol (TAG) molecular species, thermal behavior, volatile lipid oxidation products, solid fat contents, and oxidative stability were compared. When 8:0 was the acyl donor, the 1:3.03 and 1:4.58 ratios resulted in incorporation of 20 and 30 mol% 8:0, respectively. With 18:0 as the acyl donor, the 1:1.32 and 1:2.41 ratios led to incorporation of 20 and 30 mol% 18:0, respectively. The 1:3:1 ratio SL had a crystallization onset ( C 0 ) of 15.3 °C and a melting completion ( M c ) of 33.1 °C. The physicochemical properties of these SL suggest that some may be useful in formulating food products such as margarines and spreads.
author2 National Institute of Food and Agriculture
format Article in Journal/Newspaper
author Willett, Sarah A.
Martini, Silvana
Akoh, Casimir C.
spellingShingle Willett, Sarah A.
Martini, Silvana
Akoh, Casimir C.
Enzymatic Modification of Menhaden Oil to Incorporate Caprylic and/or Stearic Acid
author_facet Willett, Sarah A.
Martini, Silvana
Akoh, Casimir C.
author_sort Willett, Sarah A.
title Enzymatic Modification of Menhaden Oil to Incorporate Caprylic and/or Stearic Acid
title_short Enzymatic Modification of Menhaden Oil to Incorporate Caprylic and/or Stearic Acid
title_full Enzymatic Modification of Menhaden Oil to Incorporate Caprylic and/or Stearic Acid
title_fullStr Enzymatic Modification of Menhaden Oil to Incorporate Caprylic and/or Stearic Acid
title_full_unstemmed Enzymatic Modification of Menhaden Oil to Incorporate Caprylic and/or Stearic Acid
title_sort enzymatic modification of menhaden oil to incorporate caprylic and/or stearic acid
publisher Wiley
publishDate 2019
url http://dx.doi.org/10.1002/aocs.12227
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https://onlinelibrary.wiley.com/doi/pdf/10.1002/aocs.12227
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https://aocs.onlinelibrary.wiley.com/doi/am-pdf/10.1002/aocs.12227
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op_source Journal of the American Oil Chemists' Society
volume 96, issue 7, page 761-775
ISSN 0003-021X 1558-9331
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op_doi https://doi.org/10.1002/aocs.12227
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