This invention relates to algal biochemistry, and more specifically, to algal omega 7 compositions.
Provided herein are exemplary algal omega 7 compositions, including algal fatty acid compositions comprising by dry weight from about approximately 0.5% to about approximately 99% C16:1 n7 palmitoleic acid (POA). Such algal compositions may also include (either individually or any combination of) by dry weight: from about approximately 0% to about approximately 10% saturated fatty acids; from about approximately 0% to about approximately 99% arachidonic acid; from about approximately 0% to about 99% docosahexaenoic acid; and/or from about approximately 0% to about approximately 99% eicosapentaenoic acid.
Provided herein are also exemplary algal omega 7 compositions, including algal fatty acid compositions comprising by dry weight from about approximately 0.5% to about approximately 99% C16:1 n7 palmitoleic acid (POA). Such algal compositions may also include (either individually or any combination of) by dry weight: from about approximately 0% to about approximately 10% saturated fatty acids; from about approximately 0% to about approximately 10% arachidonic acid; substantially no (i.e. less than approximately 0.5%) docosahexaenoic acid; and/or from about approximately 0% to about approximately 10% eicosapentaenoic acid.
Further exemplary algal fatty acid compositions may include by dry weight about approximately 90% palmitoleic acid, less than about approximately 10% saturated fatty acids, less than about approximately 10% arachidonic acid, substantially no docosahexaenoic acid, and less than about approximately 10% eicosapentaenoic acid.
The algal palmitoleic acid compositions described herein may be desaturated (i.e. removing the saturated fatty acids from the monounsaturated and/or polyunsaturated fatty acids) from saturated algal compositions comprising by total weight approximately 50% POA, approximately 50% palmitic acid (PA) and substantially no DHA. The saturated algal compositions may result from the processing of total algal oil compositions comprising by total weight approximately 30% EPA, approximately 27% POA, approximately 23% PA, less than approximately 10% ARA, and substantially no DHA.
The saturated algal compositions may also result from the processing of total algal oil compositions comprising by total weight approximately 30% EPA, approximately 27% POA, less than approximately 20% saturated fats, less than approximately 10% ARA, and substantially no DHA.
The saturated algal compositions may also result from the processing of total algal oil compositions comprising by total weight from between approximately 0% EPA and 99% EPA, from between approximately 0% POA and 99% POA, less than approximately 20% saturated fats, from between approximately 0% ARA and 99% ARA, and from between approximately 0% DHA and 99% DHA.
A fatty acid is a carboxylic acid with a long aliphatic tail (chain), which is either saturated or unsaturated. Most naturally occurring fatty acids have a chain of an even number of carbon atoms, from 4 to 28. Saturated fatty acids have no double bonds between carbon atoms. Unsaturated fatty acids have one or more double bonds between carbon atoms. When counting from the terminal methyl carbon toward the carbonyl carbon on an unsaturated fatty acid, the first double bond signifies the omega double bond, such as observed in omega 3, omega 6, or omega 7 fatty acids.
Palmitoleic acid (POA) is an omega-7 monounsaturated fatty acid with a 16-carbon chain with one double bond, denoted as C16:1 n7. A beneficial fatty acid, it has been shown to suppress inflammation. Dietary sources of omega-7 are found in animal and plant sources, including sea buckthorn berries, macadamia nuts, cold water fish and dairy fat. These sources, however, are not concentrated and/or purified sources of POA and often contain a mixed fatty acid profile of saturated and polyunsaturated fats.
Palmitic acid (PA) is a saturated fatty acid with a 16-carbon chain and no double bonds, denoted as C16:0. Consumption of saturated fats such as palmitic acid is believed to increase the risk of developing diabetes, obesity, stroke and cardiovascular diseases.
Alpha linolenic acid (ALA) is an omega-3 polyunsaturated fatty acid (PUFA) with an 18-carbon chain and three cis double bonds. The first double bond is located at the third carbon from the methyl end of the fatty acid chain, denoted as C18:3 n3.
Arachidonic acid (ARA) is an omega-6 PUFA with a 20-carbon chain and four cis-double bonds; the first double bond is located at the sixth carbon from the omega end. ARA is also denoted as C20:4 n6. Examples of dietary sources of omega-6 PUFAs include refined vegetable oils, such as corn and soy oil, seeds and nuts and the oils extracted from them. Consumption is therefore sufficient in the average diet.
Eicosapentaenoic acid (EPA) is an omega-3 fatty acid PUFA with the connotation C20:5 n3. It is a carboxylic acid with a 20-carbon chain and five cis double bonds; the first double bond is located at the third carbon from the omega end.
Docosahexaenoic acid (DHA) is an omega-3 fatty acid PUFA. It is a carboxylic acid with a 22-carbon chain and six cis double bonds; the first double bond is located at the third carbon from the omega end. DHA is also denoted as C22:6 n3.
Provided herein are exemplary algal omega 7 compositions, including algal fatty acid compositions comprising by dry weight from about approximately 0.5% to about approximately 99% C16:1 n7 palmitoleic acid (POA). Such algal compositions may also include (either individually or any combination of) by dry weight: from about approximately 0% to about approximately 20% saturated fatty acids; from about approximately 0% to about approximately 99% arachidonic acid; from about approximately 0% to about 99% docosahexaenoic acid; and/or from about approximately 0% to about approximately 99% eicosapentaenoic acid.
The various exemplary algal omega 7 compositions provided herein may comprise by dry weight from about approximately 0.5% to about approximately 99% palmitoleic acid. Such algal compositions may also include (either individually or any combination of) by dry weight: from about approximately 0% to about approximately 20% saturated fatty acids; from about approximately 0% to about approximately 10% arachidonic acid; substantially no (i.e. less than approximately 0.5%) docosahexaenoic acid; and/or from about approximately 0% to about approximately 10% eicosapentaenoic acid.
Additionally, the various exemplary algal omega 7 compositions provided herein may further be in ethyl ester form. Such ethyl esters are derived by reacting free fatty acids with ethanol. Called esterification, the resulting ethyl ester allows for the fractional distillation (concentration) of the long chain fatty acids at lower temperatures. This step allows for the selective concentration of the fatty acids to levels greater than found in nature.
The ethyl ester forms of the various exemplary algal omega 7 compositions provided herein may be converted to a triglyceride form by performing an enzymatic reaction with the ethyl ester form in the presence of glycerol, heating under a vacuum, and filtering out the enzymes. Per some exemplary methods, immobilized lipase enzymes may be those isolated from Candida antarctica and/or commercially supplied by Novozyme or Sigma Aldrich.
The algal palmitoleic acid compositions described herein may be desaturated (i.e. removing the saturated fatty acids from the monounsaturated and/or polyunsaturated fatty acids) from saturated algal compositions comprising by total weight approximately 50% POA, approximately 50% palmitic acid (PA) and substantially no DHA. The saturated algal compositions may result from the processing of total algal oil compositions comprising by total weight approximately 30% EPA, approximately 27% POA, approximately 0% to 20% saturated fats, less than approximately 10% ARA, and substantially no DHA.
The saturated algal compositions may also result from the processing of total algal oil compositions comprising by total weight approximately 30% EPA, approximately 27% POA, less than approximately 20% saturated fats, less than approximately 10% ARA, and substantially no DHA.
The saturated algal compositions may also result from the processing of total algal oil compositions comprising by total weight from between approximately 0% EPA and 99% EPA, from between approximately 0% POA and 99% POA, less than approximately 10% saturated fats, from between approximately 0% ARA and 99% ARA, and from between approximately 0% DHA and 99% DHA.
In various embodiments, various algae species may be the source of the compositions provided herein. Algae are mostly aquatic photosynthetic organisms that range from microscopic flagellate to giant kelp. Algae may be loosely grouped into seven categories: Euglenophyta (euglenoids), Chrysophyta (golden-brown algae), Pyrrophyta (fire algae), Dinoflagellata, Chlorophyta (green algae), Rhodophyta (red algae), Paeophyta (brown algae), and Xanthophyta (yellow-green algae). Lipid extracted from any algae genus may be used in the various embodiments of the present invention, including Amphora, Anabaena, Anikstrodesmis, Botryococcus, Chaetoceros, Chlorella, Chlorococcum, Cyclotella, Cylindrotheca, Dunaliella, Emiliania, Euglena, Glossomastix, Haematococcus, Isochrysis, Monochrysis, Monoraphidium, Nannochloris, Nannochloropsis, Navicula, Nephrochloris, Nephroselmis, Nitzschia, Nodularia, Nostoc, Oochromonas, Oocystis, Oscillatoria, Pavlova, Phaeodactylum, Picochloris, Platymonas, Pleurochrysis, Porphyra, Pseudoanabaena, Pyramimonas, Scenedesmus, Stichococcus, Synechococcus, Synechocystis, Tetraselmis, Thalassiosira, and Trichodesmium.
An exemplary total algal oil composition, such as the exemplary total algal oil composition shown in
At step 210, 100 milliliters (mls) of the exemplary saturated algal composition is chilled at 4° C. for 24 hours, resulting in formation of transparent crystals as stoutly needles.
At step 220, the mixture comprising the transparent crystals is vacuum-filtered through a whatman #1 paper filter, and the cake is blotted with kimwipes to remove interstitial liquid.
At step 230, the filtered liquid phase is brought to −3° C. for 24 hours, and a second crop of crystals is formed as described above.
At step 240, the filtered liquid phase is brought to −10° C. for 24 hours, and a third crop of crystals is formed, these crystals being smaller and rounder than earlier crops.
At step 250, the filtered liquid phase is then brought to −20° C. for 24 hours, and forms a turbid suspension which is filtered.
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While various embodiments have been described above, it should be understood that they have been presented by way of example only, and not limitation. Thus, the breadth and scope of a preferred embodiment should not be limited by any of the above-described exemplary embodiments.
The present application claims the benefit and priority of U.S. Provisional Patent Application Ser. No. 61/800,114 filed on Mar. 15, 2013 and titled “(EPA) Algal Biomass and Oil Compositions and Impact on Health,” which is hereby incorporated by reference. The present application claims the benefit and priority of U.S. Provisional Patent Application Ser. No. 61/800,029 filed on Mar. 15, 2013 and titled “Microalga Species and Industrial Applications,” which is hereby incorporated by reference. The present application is related to U.S. Non-Provisional patent application Ser. No. ______, filed on ______ concurrently with the present application and titled “Algal Oil Compositions,” which is hereby incorporated by reference. The present application is related to U.S. Non-Provisional patent application Ser. No. ______, filed on ______ concurrently with the present application and titled “Conversion of Free Fatty Acids to Ethyl Esters,” which is hereby incorporated by reference. The present application is related to U.S. Non-Provisional patent application Ser. No. ______, filed on ______ concurrently with the present application and titled “Algal Omega 7 and Algal Omega 3 Blend Compositions,” which is hereby incorporated by reference. The present application is related to U.S. Non-Provisional patent application Ser. No. ______, filed on ______ concurrently with the present application and titled “Compositions and Methods for Utilization of Algal Compounds,” which is hereby incorporated by reference.
Number | Date | Country | |
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61800114 | Mar 2013 | US | |
61800029 | Mar 2013 | US |