Patent Application
20160270415
The application falls within the field of biochemistry and food processing, relating to modified algal oil bodies, methods for stabilizing algal oil bodies, and methods for improving the oxidation resistance of the same.
Micro-algae are a class of important marine biological resource rich in nutrients such as fat, protein, astaxanthin and the like. Micro-algal oil can be used to treat cardiovascular and cerebrovascular diseases, reduce blood pressure, protect against cancer, and regulate the function of the immune system, with eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) contained therein being of the most interest and commonly used in infant milk powder and health food. Additionally, in recent years, extracting algal oils from micro-algae and converting them into biofuels becomes a promising investigation due to affects from energy crisis (Michael H, et al., Biofuels from algae: challenges and potential, Biofuels, 2010, 1: 763-784).
Current methods for extracting micro-algal oils are mainly chemical methods, which generally comprise extracting micro-algal fermentation products by chemical agents, e.g. n-hexane-. These lead to risks of environmental pollution.
EP 1952695 has disclosed a method for extracting algal oils by utilizing oil bodies, comprising firstly dissolving dry micro-algae with sucrose solution, grinding the solution, and eluting by buffer solutions containing salt ions to obtain purified algal oil bodies. By detecting the properties of the algal oil bodies thus obtained, it was found that the optimal particle size of the algal oil bodies is within the range of 0.5-30 μm. However, the broad range of the particle size may readily lead to aggregation of droplets of algal oils and oil leakage under normal temperature. Thus, the oil bodies are not suitable for subsequent processing and application of the product (Ghislain Y C, et al., Oil bodies and method of producing such oil bodies, EP1952695, 2007 Jan. 31).
Nguyen et al (Nguyen H M, et al. Proteomic profiling of oil bodies isolated from the unicellular green micro-alga Chlamydomonas reinhardtii: With focus on proteins involved in lipid metabolism. 2011, 11:4266-73) extracts algal oil bodies by mimicking the method for extracting oil bodies from plant. However, the method has complicated steps, involving addition of a lot of protease inhibitors, use of many buffers and organic reagents, many times of centrifugation, before obtaining the oil bodies. This method is time-consuming, and the protease inhibitors are expensive.
There is an urgent need in the art for an improved method for extracting algal oil body(ies), a method for improving the oxidation resistance of an algal oil body and/or a method to stabilize an algal oil body to prevent oil leakage.
Therefore, in a first aspect, a composition comprising an algal oil body is provided, wherein said composition comprises an algal oil body, a phospholipid, and an oil body protein.
In a second aspect, a method for stabilizing an algal oil body and/or preventing an algal oil body from oil leakage is provided, wherein said method comprises adding a phospholipid and an oil body protein to the algal oil body.
In a third aspect, a method for improving the oxidation resistance of an algal oil body is provided, wherein said method comprises adding an oil body protein into the algal oil body.
In a fourth aspect, a modified algal oil body having a main particle size distribution in the range of 1.5-3 μm is provided. Preferably the algal oil body is prepared by the methods disclosed in the subject application.
The inventors of the present application found that modified algal oil bodies, which are more stable, could be obtained by adding an oil body protein and a phospholipid into the algal oil bodies. Additionally, the oil body protein can be used as an anti-oxidant for the algal oil body to confer oxidation resistance to the algal oil body.
Algal oil body is an oil body structure derived from micro-algae. It comprises some major lipid droplet proteins (MLDP) with relatively small molecule weight, but does not contain an oil body protein from a plant oil body or protein(s) similar to the oil body protein. In some embodiments, algal oil body can be produced from oil-producing algae, such as but not limited to Schizochytrium sp., Thraustochytrium sp., Crypthecodinium sp., etc., especially Schizochytrium sp.
Oil body protein from plant can be extracted from plant, such as oil crops. In some embodiments, the processing for the oil body protein does not use chemical auxiliary agent(s) such as n-hexane. Thus, as compared to the synthetic formulations, the oil body protein of plant is natural and beneficial to health, and has potential value in application.
In some embodiments, phospholipid can be one or more of phosphatidylcholine, phosphatidylinositol, phosphatidylethanolamine, phosphatidylserine, and the like. A composition comprising the aforementioned phospholipid(s) can also be used, which may be, such as compound phosphatide (including but not limited to soybean phospholipid) or lecithin.
Therefore, in a first aspect, a composition comprising an algal oil body is provided, which comprises an algal oil body, a phospholipid and an oil body protein. The oil body protein can be an oil body protein of a plant of any source. In one embodiment, the oil body protein is obtained from oil crops, including but not limited to oil body protein from peanut, oil body protein from soybean, oil body protein from rapeseed, oil body protein from sesame, oil body protein from sunflower seed, oil body protein from olive, oil body protein from palm, oil body protein from seed of tea tree, or a mixture of any of the above oil body proteins. In another embodiment, the oil body protein is an oil body protein from peanut.
In some embodiments, the algal oil body can be produced from oil-producing algae, such as but not limited to Schizochytrium sp., Thraustochytrium sp., Crypthecodinium sp., etc., especially Schizochytrium sp.
In one embodiment, in the modified algal oil body, the algal oil body comprises 50-100 parts by weight, preferably 70-100 parts by weight, more preferably 90-100 parts by weight, such as but not limited to 91, 92, 93, 94, 95, 96, 97, 98 and 99 parts by weight, the phospholipid comprises 0.5-10 parts by weight, preferably 0.5-5 parts by weight, 1.0-2.5 parts by weight, or 0.5, 1, 1.5, or 2 parts by weight; and the oil body protein comprises 0-10 parts by weight, such as 2-5 parts by weight, 2.5-4.5 parts by weight, or 2, 3 or 4 parts by weight. In some embodiments, the modified algal oil body has improved structural stability and reduced oil leakage.
In a second aspect, a method for stabilizing an algal oil body is provided, wherein the method comprises adding a phospholipid and an oil body protein into the algal oil body.
As described above, the oil body protein can be an oil body protein from a plant of any source. In one embodiment, the oil body protein is from oil crops. In another embodiment, the oil body protein is an oil body protein from peanut.
In some embodiments, the algal oil body can be produced from oil-producing algae, such as but not limited to Schizochytrium sp., Thraustochytrium sp., Crypthecodinium sp., etc., especially Schizochytrium sp.
In some embodiments, a suitable amount of the phospholipid and oil body protein can be added to the algal oil body simultaneously to stabilize its structure and to prevent oil leakage. In some embodiments, in the method for stabilizing the algal oil body, the algal oil body comprises 50-100 parts by weight, preferably 70-100 parts by weight, more preferably 90-100 parts by weight, such as 91, 92, 93, 94, 95, 96, 97, 98 and 99 parts by weight, the phospholipid added comprises 0.5-10 parts by weight, preferably 0.5-5 parts by weight, more preferably 1.0-2.5 parts by weight, such as 0.5, 1, 1.5, or 2 parts by weight; and the oil body protein added comprises 0.5-10 parts by weight, preferably 2-5 parts by weight, more preferably 2.5-4.5 parts by weight, such as 2, 3 or 4 parts by weight.
In some embodiments, the method for stabilizing an algal oil body further comprises sonic oscillation of a mixture of the algal oil body, phospholipid and oil body protein. In another embodiment, the sonic oscillation lasts 5-30 seconds, preferably 10-25 seconds, such as about 10, 15 or 20 seconds. In another embodiment, after sonic oscillation of the mixture of the algal oil body, phospholipid and oil body protein for the above indicated time, the mixture is subjected to an ice bath for 1-10 minutes, such as about 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 minutes. In some embodiments, the sonic oscillation and the treatment with ice bath are repeated for 2-5 times, such as 2, 3, 4 or 5 times.
The structure of the algal oil body per se is not stable. Its particle size is mainly in the range of about 2-4 μm, and the distribution range is relatively wide. This leads to aggregation of oil droplets and oil leakage under normal temperature. Thus, the algal oil body is not suitable for subsequent processing and application.
The inventors of the present application surprisingly found that, addition of both phospholipid and oil body protein to an algal oil body could make the particle size of the algal oil body be close to the particle size of a natural plant oil body, which is in average 2 μm, and to make the particle size be mainly distributed within 1.5-3.5 μm, preferably 1.5-2.5 μm, more preferably 1.5-2.0 μm. Impurity peaks were reduced or disappeared. The distribution range was narrowed. Consequently, the modified oil body is obtained. Without being bound to any theory, the above characteristics of the modified algal oil body may be attributable to the oil body proteins embedded in the monomolecular layer of phospholipid, which can package the algal oil more sufficiently. This indicates that a more uniform and stable monodisperse emulsion system could be formed after addition of phospholipid and oil body protein into an algal oil body, which could effectively prevent the algal oil from aggregation and leaking out.
In a third aspect, a method for improving the oxidation resistance of an algal oil body is provided, wherein the method comprises adding an oil body protein into the algal oil body, and optionally adding a phospholipid.
In one embodiment, the oil body protein can be an oil body protein from a plant of any source. In one embodiment, the oil body protein is from oil crops, preferably the oil body protein is an oil body protein from peanut.
In some embodiments, the algal oil body can be produced from oil-producing algae, such as but not limited to Schizochytrium sp., Thraustochytrium sp., Crypthecodinium sp., etc., especially Schizochytrium sp.
In some embodiments, in the method of improving the oxidation resistance of an algal oil body, the algal oil body comprises 50-100 parts by weight, preferably 70-100 parts by weight, more preferably 90-100 parts by weight, such as but not limited to 91, 92, 93, 94, 95, 96, 97, 98 and 99 parts by weight, the phospholipid added comprises 0-10 parts by weight, preferably 0-5 parts by weight, 0-2.5 parts by weight, such as 0.5, 1, 1.5, or 2 parts by weight; and the oil body protein added comprises 0.5-10 parts by weight, preferably 2-5 parts by weight, more preferably 2.5-4.5 parts by weight, or 2, 3 or 4 parts by weight.
In some embodiments, the method for improving the oxidation resistance of an algal oil body further comprises sonic oscillation of a mixture of an algal oil body, a phospholipid and an oil body protein. In another embodiment, the sonic oscillation lasts 5-30 seconds, preferably 10-25 seconds, such as about 10, 15 or 20 seconds. In another embodiment, after sonic oscillation of the mixture of an algal oil body, a phospholipid and an oil body protein for the above indicated time, the mixture is subjected to an ice bath for 1-10 minutes, such as about 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 minutes. In some embodiments, the sonic oscillation and the treatment with ice bath are repeated for 2-5 times, such as 2, 3, 4 or 5 times.
In a fourth aspect, a modified algal oil body having a particle size distributing mainly in the range of 1.5-3.5 μm is provided. Preferably, the modified algal oil body is prepared by the methods according to the above second or third aspect of the present application, and preferably consists of the composition as described in the first aspect.
In some embodiments, the particle size of the algal oil body is mainly distributed in the range of 1.5-2.5 μm, preferably 1.5-2.0 μm.
In the present invention, “a particle size (of the algal oil body) distributing mainly in the range of” or similar expression means the distribution range of the particle size of 50% or more, preferably 60% or more, 70% or more, 80% or more, more preferably 90% or more of the algal oil body.
The natural algal oil body obtained after extraction is readily oxidized, as evidenced by increased conjugated diene value and peroxide value, for evaluating the primary oxidation degree, and anisidine value, for evaluating the amount of secondary oxidative products, over time. In contrast, the algal oil body of the subject invention, in which an oil body protein is added, has improved oxidation resistance ability. The amount of the primary oxidative product is effectively reduced and the amount of the secondary oxidative product is not changed within 48 hours. These demonstrate that addition of the oil body protein can increase the oxidation resistance of the algal oil body, which makes its structure more stable and allows it to be stored for a prolonged time.
Additionally, the subject application also provides a method for extracting an algal oil body, comprising subjecting a fermentation liquid of a micro-alga from Schizochytrium sp., Thraustochytrium sp., Crypthecodinium sp., etc., to grinding and shearing, and adding thereinto a phosphate buffer solution containing 0.6 M sucrose, and then centrifugating the mixture. In some embodiments, the micro-alga is from Schizochytrium sp.
As compared to conventional chemical methods for extracting oils, extracting algal oils by algal oil body(ies) is more environmental protective with no pollution to the environment and is applicable for industrial production. As compared to the method for extracting an algal oil body as disclosed by Nguyen et al, the methods of the subject application have less steps, in particular, skip the addition of protease inhibitors, the use of organic solvents, and several times of centrifugations, which can greatly reduce costs. As compared to EP 1952695, the subject invention directly extracts an algal oil body from a fermentation liquid of a micro-alga from Schizochytrium sp., Thraustochytrium sp., Crypthecodinium sp., etc., thus skips the step of dissolving the micro-alga. This makes all steps be performed in an aqueous phase, thus avoiding the step of eluting by buffer and reducing waste of algal oils.
In the subject application, the term “consisting essentially of” or similar expression indicates a partially open-ended mode of definition, which does not exclude the presence of one or more other non-essential elements, components or steps, as long as these other non-essential elements, components or steps do not virtually affect the property of the invention determined by the main elements, components or steps as listed above. Furthermore, the terms “comprise” or “contain” includes “consist of” and “consist essentially of” or similar expressions.
The term “a” or “an” is generally intended to mean “one or more” unless otherwise indicated.
The contents of all references and documents cited therein are incorporated in the subject invention by reference.
The invention will be further illustrated in the following examples by making reference to the Figures. The following examples are for illustrating the invention, and are not intended to make any limitation to the scope of the invention, which will be limited by the claims.
Phosphatidylcholine, phosphatidylinositol, phosphatidylethanolamine and phosphatidylserine used in the examples were all purchased from Sigma.
Culture media used in the examples include:
Seed culture medium (g/L): glucose 30.0, peptone 10.0, yeast extract 5.0, sea salt 15.0. Fermentation medium (g/L): glucose 109.7, peptone 19.2, yeast extract 20.0, sea salt 12.5.
Schizochytrium ATCC20888 was seeded to the seed culture medium and cultured at 28° C. and 200 rpm to obtain the seed solution. The seed solution was inoculated to the fermentation medium and cultured at 28° C. and 750 rpm for 96 hours to obtain the Schizochytrium fermentation liquid.
The Schizochytrium fermentation liquid (containing biomass in 100-150 g/l) was sand ground for 20 times, with each time for 5 minutes, at a shear rate of 2,500 rpm. After that, an oil body can be freed from the 200 μm sieve pores and isolated from the debris. Phosphate buffer solution (50 mM, which contains 0.6M sucrose and has a pH of 7.5), was added in a 1:1 volume ratio. The mixture was centrifugated at 10,000×g at 4° C. for 30 minutes. The solution was separated into three layers, wherein the bottom layer include the debris; the medium layer is an aqueous phase comprising a great amount of soluble proteins; and the top layer is an oil phase coated by a layer of proteins at its outer surface, both of which form the algal oil body. The algal oil body is taken out from the centrifuging tube.
Acetone was added into the algal oil body in a ratio of 1:1. The mixture was subjected to ice bath under gentle agitation for 10-15 minutes. Then, the mixture was centrifugated at 10,000 rpm, 4° C. for 10 minutes. The supernate was removed. And the precipitate was suspended in 100 mM, pH 7.5 PBS, which has the same volume as the precipitate. The suspension was centrifugated at 10,000 rpm for 30 minutes and the supernate was removed. The precipitate was washed for three times to obtain the algal protein, which is ready for detection of protein.
Peanut kernels were dimmed in 50 mM, pH 7.5 PBS overnight. One hundred grams of the dimmed peanut kernels were placed in a tissue triturator (NETZSCH Lab Horizontal Mill LMZ 0.5), homogenated at 3,000 rpm for 1 minute after adding 500 mL buffers (100 mM PBS, pH 7.5), and then homogenated at 10,000 rpm for 2 minutes for three times. The resultant mixture was filtered through a two-layer cheese cloth. The cake on the cheese cloth was pressed. The residual filter cake was ground and filtered again under the same conditions. The two filtrates were pooled and filtered through a layer of Microcloth. The finally obtained filtrate was centrifugated at 20,000×g for 30 minutes. The emulsion layer at the top of the centrifugating tube was collected, which was the crude oil body from peanut.
The crude peanut oil body was placed in a 100 mM, pH 7.5 frozen PBS solution and homogenated in high shear homogenizer SPX at 20,000 rpm for 2 minutes. After homogenation, the resultant mixture was centrifugated at 20,000×g for 5 minutes. The emulsion layer was collected, dissolved in buffer, homogenated at 20,000 rpm for 2 minutes, and centrifugated at 10,000×g for 30 minutes. The collection, dissolution, homogenation and centrifugation together formed a cycle and this cycle was repeated three times. Finally the emulsion layer was collected, which was the purified peanut oil body.
Acetone was added in a 1:1 ratio into the peanut oil body. The mixture was subjected to an ice bath with gentle agitation for 10-15 minutes. Then, the mixture was low-temperature centrifugated at 10,000×g for 10 minutes. The supernate was removed, and 100 mM PBS (pH 7.5) with the same volume as the precipitate was added to suspend the precipitate. The suspension was centrifugated at 10,000×g for 30 minutes and the supernate was removed. After washing 3 times, the purified peanut oil body protein was obtained.
The resultant purified peanut oil body protein and algal protein were diluted by 100 mM PBS, pH 7.5 in a volume ration of 5:1, respectively and then 5×SDS-PAGE loading buffer were added to each solution. The mixtures were cooked for 5 minutes. A 15% protein revolving gel and a 6.7% stacking gel were used. Electrophoresis was performed at 90 V constant voltage initially and the voltage was adjusted to 180 V after bromophenol blue migrated into the revolving gel. The power was shut off after the bromophenol blue band moved out of the gel and the electrophoresis was finished. The gel was placed into a clean vessel. Thirty milliliters of staining solution for protein electrophoresis was added and the mixture was heated in microwave oven for 2 minutes. Then, the vessel was placed on a horizontal shaking table running at 100 rpm for staining for 1 hour. The staining solution was removed and a certain amount of destaining solution was added to wash the bands 3-4 times, each 20 minutes, until the protein bands became clear.
The results of the protein electrophoresis are shown in
Two hundred micrograms of phosphatidylcholine was dissolved in chloroform and placed in a chemical hood for volatilization overnight. To the phosphatidylcholine solution, 19.6 mg algal oil bodies together with 100 μg, 200 μg, 400 μg or 800 μg peanut oil body proteins were added respectively (numbered as samples 1, 2, 3, and 4, respectively). After sonic oscillation for 20 seconds, the mixtures were placed in an ice bath for 5 minutes. Sonic oscillation was repeated for three times to form an algal oil body mixture. The samples were placed in an oven at 40° C. After 72 hours, the samples were left to stand to observe oil leakage, thereby observing their stability. The oil bodies showed cracking as treatment in oven going on. Oil leakage is defined as presence of leaked oil droplets with clear boundary between the leaked oil and the residual oil body. After treatment in the oven, different samples have different status of oil leakage.
The results are shown in
According to
Our subsequent experiments show that the stability of the algal oil body does not increase after the amount of the oil body protein reaches a certain value. The preferred weight ratio between the algal oil body and the oil body protein is 98:4. Currently, 98:10 by weight of algal oil body to oil body protein is a permissible ratio that can be used to increase the stability of the algal oil body without producing obvious off odour.
Zero micrograms, 100 μg, 200 μg and 400 μg phosphatidylcholine were dissolved respectively in chloroform and placed in a chemical hood for volatilization overnight. To the phosphatidylcholine solutions, 19.6 mg algal oil bodies and 800 μg peanut oil body proteins were added (numbered as samples 1, 2, 3, and 4, respectively). After sonic oscillation for 20 seconds, the mixtures were placed in an ice bath for 5 minutes. Sonic oscillation was repeated for three times to form an algal oil body mixture. The samples were placed in an oven at 40° C. After 72 hours, the samples were left to stand to observe oil leakage. The oil bodies showed cracking as treatment in oven going on. Oil leakage is defined as presence of leaked oil droplets with clear boundary between the leaked oil and the residual oil body. After treatment in the oven, different samples have different status of oil leakage. Results are shown in
As shown in
According to the results in Example 4, the sample in which the weigh ratio of algal oil body, phosphatidylcholine and protein is 98:1:4 was used in the comparison experiments with three control samples, control 1 comprising algal oil body and phosphatidylcholine (sob+p, 98:1, parts by weight), control 2 comprising algal oil body and peanut oil body protein (sob+ole, 98:4, parts by weight), and control 3 comprising algal oil body without adding any other component (sob, 98 parts by weight). The samples were treated as described above. Specifically, they were subjected to sonic oscillation to form mixtures and then the particle size of each sample was detected.
The statistical data of the particle size are shown in
Additionally, other experiments with different weight ratios were also performed.
According to the weight ratios of algal oil body, phosphatidylcholine to protein, the following three samples were prepared: 98:0.5:4 of algal oil body, phosphatidylcholine to protein; 98:1:4 of algal oil body, phosphatidylcholine to protein, and 98:2:4 of algal oil body, phosphatidylcholine to protein. They were treated as described above. Specifically, they were subjected to sonic oscillation to form mixtures and then the particle size of each sample was detected. The results are shown in
The results in
Another three samples were prepared according to the weight ratio of algal oil body, phosphatidylcholine to protein, which include 98:1:1 of algal oil body, phosphatidylcholine to protein; 98:1:3 of algal oil body, phosphatidylcholine to protein, and 98:1:4 of algal oil body, phosphatidylcholine to protein. They were treated as described above. Specifically, they were subjected to sonic oscillation to form mixtures and then the particle size of each sample was detected. The results are shown in
The results in
Five samples, which are algal oil (so), algal oil body (sob), algal oil body+phosphatidylcholine (sob+p, 98:1), algal oil body+peanut oil body protein (sob+ole, 98:4), and algal oil body+phosphatidylcholine+peanut oil body protein (sob+p+ole, 98:1:4), were placed into an over at 40° C. and each oxidative index was detected at every 12 hours.
I. Detection of Conjugated Diene Value (DV)
Conjugated diene value, also termed as diene value, is meant to the gram of iodine which is converted from the desired maleic anhydride in 100 g oil. Diels-Alder reaction may be taken place between maleic anhydride and the conjugated diene in the oil. Thus, the diene value is a characteristic index for identifying the conjugated system presented in the unsaturated fatty acids of the oil. Higher diene value indicates much serious oxidation of the oil.
The DV was detected as follows: 0.01-0.03 g oil or oil extract were precisely weighted, placed into a 25 ml measuring flask, and diluted with isooctane to 25 ml to prepare an oil sample solution. The solvent, isooctane, was added into the reference slot of spectrophotometer, as a blank control. The absorbance (Aλ) of the oil sample solution in the sample slot was detected at 233 nm. The equation is as follows:
wherein E is extinction value, Aλ is absorbance at 233 nm, CL is the mass of the 100 ml oil, and l is the length of the path of the cuvette.
Results are shown in
II. Detection of Peroxide Value (PV)
Peroxide value is an index indicating the primary oxidation of oil and fatty acid and the rancidity degree of the oil. Generally, higher peroxide value indicates relatively obvious rancidity. Peroxide value is meant to the content of active oxygen in 1 kg sample and is expressed as meq/kg of the peroxide.
In the subject application, the PV was determined according to GB/T5009.37-2003. Specifically, 2-3 g homogeneously mixed samples were precisely weighted and placed into a 250 ml iodine flask. A mixture of trichloromethane and glacial acetic acid (30 ml, 2:3) was added to dissolve the samples. Then, 1 ml saturated potassium iodide solution was added. The flask was tightly sealed by its bottle plug and gently shook for 0.5 minutes. The flask was then placed in dark for 3 minutes, taken out, added thereinto 100 ml water and shook up. Titration was immediately carried out by using 0.002 mol/L sodium hyposulfite standard solution. One milliliter starch indicator was added when the solution turned to light yellow. Titration was continued until the blue color faded away. The same amount of trichloromethane-glacial acetic acid solution, potassium iodide solution and water were used as blank control to perform the above test.
PV is calculated by the following equation:
wherein:
X1 is the PV of sample, expressed by g/100 g;
X2 is the PV of sample, expressed by meq/kg;
V1 is the volume of the sodium hyposulfite standard solution depleted by the sample, expressed by mL;
V2 is the volume of the sodium hyposulfite standard solution depleted by the blank control, expressed as mL;
c is the molar concentration of the sodium hyposulfite standard, expressed by mol/L;
m is the mass of the sample, expressed by gram (g);
0.1269 is the mass of iodine which corresponds to the mass of 1.00 mL sodium hyposulfite standard titration solution [c (Na2S2O3)=1.000 mol/L], expressed by gram (g);
78.8 is a conversion factor.
Table 1 lists out the PVs of five samples tested for every 12 hours in the 40° C. oven according to GB/T5009.37-2003.
The results show that after treatment in oven for 48 hours, the PV of algal oil body (sob) is at most ⅕ of the PV of the algal oil (so). The peroxide values of the algal oil body+peanut oil body protein (sob+ole) and the algal oil body+phosphatidylcholine+peanut oil body protein (sob+p+ole) are almost not changed within 48 hours, and are at most 1/20 of the PV of the algal oil (so).
The above results demonstrate that the peanut oil body protein could pack the algal oil body to produce more stable structure and to prevent algal oil body from interference from outside conditions.
III. Detection of PAV (p-Anisidine p Value)
Anisidine value is an index indicating the amount of the secondary products, unsaturated aldehydes, such as aldehydes, ketones and quinones, in the oil. If the oil contains a lot of such kind of substances, aldehydes and ketones of small molecular weight will readily be produced during heating. Anisidine value is used to evaluate the amount of secondary oxidative products α-unsaturated aldehydes and β-unsaturated aldehydes (2-alkyl aldehydes and 2,4-diene aldehydes).
In the subject application, the PAV was determined according to GB/T24304-2009. Specifically, 0.5-4.0 g oil samples (accurate to 0.001 g) were weighted, placed in a 25 ml measuring flask, dissolved and diluted with isooctane to 25 ml to prepare an oil sample solution. The solvent was loaded into the reference slot of spectrophotometer (Shanghai Tianmei, UV1000) as a blank control. The absorbance (Ab) of the oil sample solution in the sample slot was detected at 350 nm.
Five milliliters of oil sample solution were accurately sucked into a first tube, and another 5 ml of oil sample solution were accurately sucked into a second tube. One milliliter p-anisidine reagent was added by pipette accurately to each tube. The tubes were shook.
Ten minutes later, the solution from the second tube was loaded into the reference slot, as a blank control, and the oil sample solution from the first tube was loaded into the sample slot and its absorbance (As) was determined at 350 nm.
The PAV was calculated according to the following equation:
wherein:
As is the absorbance of the oil sample solution after reaction with p-anisidine reagent;
Ab is the absorbance of the oil sample solution;
W is the mass of the oil sample (g).
PAVs are shown in
Modified algal oil bodies were prepared according to the methods of Examples 4-7 by replacing phosphatidylcholine with phosphatidylinositol, phosphatidylethanolamine and phosphatidylserine, respectively. The stability, oxidation resistance and particle size of the modified algal oil bodies were detected. The results show that the algal oil bodies modified by phosphatidylinositol, phosphatidylethanolamine or phosphatidylserine have similar stability, oxidation resistance and particle size to the algal oil body modified by phosphatidylcholine. Specifically, as for the stability, addition of oil body protein can confer the algal oil body with good stability. The algal oil does not readily leak out. Under the combined action of the oil body protein and phospholipid, the algal oil body could have more uniform and ideal particle size. For oxidation resistance, addition of oil body protein could improve the oxidation resistance property of the algal oil body and reduce the primary and secondary oxidative products.
The above are merely specific examples of the subject application. The scope of the subject invention should not be limited to these examples. Any change or modification that can be conceived of by the skilled artisan without any creative work and within the technical scope disclosed in the subject application should be all included in the protection scope of the invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201310513558.5 | Oct 2013 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2014/089376 | 10/24/2014 | WO | 00 |
