Method for producing a protein preparation from sunflower seeds and protein preparation produced thereby

Abstract

In a method for producing a protein preparation from sunflower seeds, a protein-containing powder from dehulled and deoiled sunflower seeds, preferably having a protein solubility in water at pH 6 of more than 15% by weight and / or a protein solubility in water at pH 7 of more than 25% by weight, based on the protein content in the powder, is subjected to at least one extraction step with water at a pH value between 4 and 9, to obtain a liquid phase as the extract and a solid-rich phase as the raffinate. Before and / or during the extraction step, the oxygen concentration in the water is reduced to a value below 7 mg / l and / or components with antioxidant action are added to the water to reduce oxidative activity. After separation of the extract and the raffinate, the extract is concentrated and / or dried to obtain a protein preparation with a high protein content. This method allows for the production of a protein preparation of good quality, organoleptically attractive, and light color with a protein content of more than 75% by weight.

Description

[Technical field]

[0001] The present invention relates to a method for obtaining functional protein preparations from seeds, such as sunflower seeds, in particular as protein additives for food, pet food, cosmetics and industrial products, and to protein preparations produced thereby. [Background technology]

[0002] In the context of ever scarcer agricultural areas and resources, plant protein preparations are becoming increasingly important for human food and for use in animal feed. The growing demand for quality food and feed increases the need for nutritionally, physiologically and technologically functionally optimized protein preparations that can be provided simply and cheaply.

[0003] A cheap source of protein for food and feed is the press and extraction residues from sunflower oil extraction. Sunflower seeds are characterized by a hard shell with a predominantly dark coloration and an oil-containing pulp. Although it is possible to separate the shell from these feedstocks prior to oil extraction, complete or extensive separation of the shell leads to reduced yields and rates of oil extraction.

[0004] Press cakes and extract residues from sunflower oil extraction are currently mainly used as animal feed. However, their use in animal feed is limited to only a few percent of the feed, despite their high protein content. This is due in part to the very high proportion of husks in the residue, which can exceed 25% by weight. In addition, the proportion of disruptive accompanying substances, in particular the content of secondary plant components such as polyphenols, tannins or phytic acid, is very high. These components can add up to more than a few percent by weight in the residue and can significantly impair the color, taste and digestibility of the protein. Therefore, press cakes and extract residues from sunflower oil extraction are not suitable for the production of quality protein additives for food or pet food without further measures.

[0005] Sunflower seeds are generally processed with a focus on high oil yield. In this case, the seeds are first cleaned of contaminants and conditioned in terms of temperature and humidity. Usually, part of the husk is also removed. The material thus prepared is then mechanically pre-deoiled by pressing to a residual oil content of between 8% and 20%. It is then deoiled with hexane or ethanol or supercritical CO. 2 The remaining oil is extracted from the press cake using another solvent such as ethanol, etc. A residue is left with an oil content of less than 3% by weight and a protein content between 40% and 55% by weight depending on the shell fraction.

[0006] According to the prior art, sunflower seeds are mainly partially shelled and pressed. In partial shelling, approximately 50% by weight of the shell contained in the seeds is left in the raw material before deoiling, which corresponds to an average residual shell content before pressing of more than 15% by weight. According to the prior art, a shell proportion of at least 10% by weight is considered necessary, especially for pressing, in order to facilitate the draining of the oil from the press, thereby increasing the pressing speed and reducing costs.

[0007] For some years now, there has also been an approach to obtain protein preparations in the form of protein powders or protein concentrates from residues of sunflower oil extraction, making them available for food and fine feed applications. Several publications describe the production of protein preparations from sunflower seeds. These protein preparations are obtained by dry-technical or wet-technical processing (e.g. with the use of solvents), whereby proteins remain in the residue. However, the use of the residues for some food applications is limited by the high proportion of undesirable accompanying substances and the high crude fiber content. Therefore, the scope of application of most protein powders and protein concentrates is limited and they can only be used at low concentrations in feed.

[0008] DE 10 200 03 13 56 A1 describes, inter alia, a method for obtaining sunflower protein as a protein-rich food or feed. For the production of the feed, partially dehulled sunflower seeds with a residual husk content of more than 5% by weight are used. Pressing of the seeds is carried out to an oil content of from 8% to 18% by weight and a protein content of from 30% to 45% by weight based on the dry weight. The influence of a residual husk content of more than 5% by weight on the digestibility of the protein is not investigated. Moreover, here too one has to start from the premise that the high crude fibre content and the high chlorogenic acid content of the product can significantly limit its acceptability as a feed and therefore its usefulness.

[0009] US Pat. No. 5,399,633 describes a method for producing a protein preparation from dehulled sunflower seeds. In this method, sunflower seeds are dehulled until a residual shell content of less than 5% by weight or dehulled sunflower seeds with a residual shell content of less than 5% by weight are prepared. Mechanical partial deoiling of the dehulled sunflower seeds is carried out by squeezing until the fat or oil content of the dehulled sunflower seeds is in the range between 10% and 35% by weight. After carrying out one or more extraction steps with at least one solvent, a deoiled protein-containing powder is obtained as protein preparation. The protein preparation has very advantageous visual and functional properties, which allow its direct use in the food or feed sector. Due to the low temperatures during squeezing below 80° C. and desolvation below 90° C., the method preserves good technical and functional properties and provides a low degree of denaturation, which gives a very good digestibility and bioavailability. However, the low protein content of 55% to 65% by weight and the proportion of insoluble crude matter clearly limit the possible uses of the preparations, so that, for example, protein-rich sports nutrition or clear drinks cannot be obtained with these preparations.

[0010] Recently, preparations have been published in the literature, and protein preparations from sunflower seeds with higher protein contents, above 70% by weight, and in some cases even above 90% by weight, are also available on the market. The availability of such preparations is certainly significantly higher than that of powders and concentrates, due to the high protein proportion, but L * a * b * L less than 60 measured in color space * Based on the low brightness values ​​as a function of the total protein content, discoloration (green, beige-brownish hues), low protein solubility below 30% and taste defects, even these preparations cannot be widely used in sensory demanding applications. Moreover, these methods are often very expensive and consist of several solvent extractions (e.g., J. Soc. Chem. Soc. 1999, 143:1311-1323) and / or aqueous extractions using various pH values ​​and various precipitation steps. Often, in this case, the sunflower seeds are deoiled directly with solvents without a prior subsequent partial mechanical deoiling, even though they are further dehulled, further reducing the economic and industrial viability of the method.

[0011] Furthermore, approaches are known to improve the solubility of sunflower proteins when obtained by extraction by the addition of sodium chloride or other salts (Non-Patent Documents 2 and 3). However, such preparations also have a very salty taste after extraction in aqueous solutions with high salt concentrations, so that such methods also do not result in attractive preparations and incur very high costs. [Prior art documents] [Patent documents]

[0012] [Patent Document 1] European Patent No. 2885980 [Patent Document 2] International Publication No. 2010 / 097238 [Non-patent literature]

[0013] [Non-Patent Document 1] Saeed und Cheryan, 1988, Sunflower Protein concentrates and isolates low in polyphenols and phytates, Journal of Food Science, 53 (4), 1127-1131 [Non-Patent Document 2] Pickardt et al. 2009, Optimization of mild-acidic protein extraction from defatted sunflower (Helianthus annuus L.) meal, Food Hydrocolloids, 23 (7), 1966-1973 [Non-Patent Document 3] Pickardt et al. 2015, Pilot plant preparation of light-coloured protein isolates from de-oiled sunflower (Helianthus annuus L.) press cake by mild-acidic protein extraction and polyphenol adsorption, Food Hydrocolloids, 44, 208-219 Summary of the Invention [Problem to be solved by the invention]

[0014] The object of the present invention was to provide an economical method for producing a qualitatively good and organoleptically attractive protein preparation from sunflower seeds with a protein content of more than 75% by weight and excellent techno-functional properties. The preparation should be highly attractive in terms of color and taste and should have excellent techno-functional properties. Furthermore, the preparation should be versatile in food and feed due to its high protein content. [Means for solving the problem]

[0015] The above problem is solved by the method according to claim 1. To The above method solves the problem. of Advantageous embodiments are the subject matter of the dependent claims.

[0016] Using the method described below, it is surprisingly possible to obtain at least two protein-rich fractions from sunflower seeds during processing, one of which has a protein content of more than 75% by weight. These two or more fractions meet high organoleptic requirements and contain in total more than 50% by weight, in an advantageous embodiment more than 70% by weight, particularly preferably more than 90% by weight, of the protein from the sunflower flour input to the process, where the sunflower flour has a protein content of more than 35% by weight, advantageously between 45% and 60% by weight, particularly preferably between 48% and 57% by weight. The high utilization of the protein added to the input of the method allows a high degree of economy compared to existing methods according to the prior art, since, unlike other methods, some fractions can be utilized as protein-rich and organoleptically attractive protein-rich food additives.

[0017] For the method according to the invention, firstly a protein-containing powder is prepared, obtained from dehulled and deoiled sunflower seeds, with an oil content of less than 8% by weight, preferably less than 4% by weight, particularly preferably less than 2% by weight (measured by the Soxhlet method AOAC 963.15, respectively) and a shell proportion of less than 10% by weight, preferably less than 5% by weight, particularly preferably less than 1% by weight or less than 0.1% by weight, where said deoiling comprises at least one mechanical step by means of a screw press or an extruder and optionally deoiling with an organic solvent such as ethanol or hexane. The powder used is characterized by a protein content by dry weight of more than 35% by weight, preferably more than 45% by weight, particularly preferably more than 48% by weight (determined according to Dumas method section 64 LFBG L 01.00-60 with conversion factor 6.25) and good protein solubility.

[0018] Preferably, powders are used which have a protein solubility in water at pH 6 of more than 15% by weight, advantageously more than 20% by weight, particularly advantageously more than 25% by weight, based on the protein content in the powder, and / or a protein solubility in water at pH 7 of more than 25% by weight, advantageously more than 30% by weight, particularly advantageously more than 35% by weight. In this case, the protein determination for determining the protein solubility is carried out according to the protein solubility determination according to CV Morr, and the determination of the NSI value is carried out according to the official AOCS method (Ba 11-65; 1993) or AACC method (46-23; 1990).

[0019] To be able to obtain powders with such high protein solubility, particularly mild conditions, especially during deoiling by screw press or extruder and deoiling by solvent, and a significant reduction of interfering impurities that may affect solubility, should be ensured. However, it has surprisingly been found that in the powders used, a certain residual solvent content does not adversely affect the protein solubility in the powder as expected, but rather a certain amount of solvent in the powder has a positive effect on subsequent further processing steps. In this case, the solubility is particularly good when the residual content of at least one organic solvent (ethanol or propanol or methanol or hexane) is more than 0.001% by weight, preferably more than 0.01% by weight, particularly preferably more than 0.05% by weight or 0.1% by weight. Within this concentration range, with an upper limit of about 1% by weight, it is clear that the solubility of the protein increases as the solvent proportion in the powder increases.

[0020] The particles of the powder are preferably milled before extraction, in which case the D90 (particles with 90% of the mass less than a specified particle size) (measured by laser diffraction in n-butanol) is in the range of 100 μm to 2500 μm, preferably the D90 is less than 500 μm or less than 250 μm. If the D90 is reduced, for example by further milling, to less than 100 μm, particularly preferably to less than 50 μm, the dissolution of the protein from the powder can be further accelerated.

[0021] Since an aqueous extraction step is carried out in the further course of the method according to the invention, a high protein concentration in the powder and preferably good solubility of the proteins contained therein are advantageous. High protein solubility is achieved by not adjusting the temperature during pressing, deoiling with organic solvents and desolventization too high, thereby keeping the protein solubility in the residue at a high level. All these steps are carried out at temperatures below 120°C, better below 100°C, particularly advantageously below 80°C, which largely avoids thermal damage and maintains protein solubility. It is therefore advantageous to use powders that have been pressed, deoiled and desolventized at temperatures below the abovementioned temperatures.

[0022] As already mentioned further above, the protein-containing powder from deoiled sunflower seeds has a shell content of less than 10% by weight, preferably less than 5% by weight or less than 1% by weight, particularly preferably less than 0.5% by weight or even less than 0.1% by weight. In particular, the shell-free or almost shell-free powder allows the proteins from the extract or at least one of the extracts according to the invention to be utilized for food applications, as well as the proteins from the remaining raffinate.

[0023] In the method according to the invention, at least one aqueous extraction is carried out on the prepared sunflower flour. For this, the flour and an excess of a defined amount of water (for example a ratio of water to flour of more than 3:1, better still more than 5:1, particularly advantageously 10 or more:1) are mixed in a stirred vessel and, after a period of time (advantageously between 10 and 60 minutes) the suspension is separated into a liquid phase (extract) and a solid-rich phase (raffinate) using a continuously operating centrifuge, preferably a decanter. In this case, the extraction, the separation of the two phases as well as the further processing and optional drying of the two fractions are carried out with sufficient exclusion of oxygen and / or with the addition of antioxidants and / or reducing agents, so that after the extraction and optional drying, it is possible to obtain a good quality, light-colored protein preparation with good technical and functional properties, respectively, from one of the extracts (or one of the extracts) and, in the case of a sufficiently low husk proportion, from the raffinate. In this case, the two fractions are separated after analytical milling into L* a * b * In terms of color space, L is greater than 70, in an advantageous embodiment greater than 80, particularly preferably greater than 90. * Indicates the value.

[0024] As already mentioned, in order to simultaneously obtain two good quality protein preparations with light color from a powder, on the one hand, a low shell percentage as well as a high protein percentage in the powder is necessary. A good protein solubility (solubility parameters as above) can further improve the results. On the other hand, according to the invention, the extraction must be carried out in such a way that oxidation of the sunflower seed components is largely avoided or that the components prone to oxidation are sufficiently separated from the two fractions, for example by a prior aqueous extraction of the powder.

[0025] This is particularly advantageously carried out by carrying out at least one aqueous extraction (preferably at a pH value of less than 8, advantageously less than 7, particularly advantageously less than 6) under exclusion of air, i.e. by applying a vacuum or by using nitrogen, argon, CO 2 This can be achieved by adding an inert gas, or another inert gas, and / or by using food-approved antioxidants and / or reducing agents, such as sodium bisulfite, sodium sulfite, or cysteine. When oxidation is significantly reduced or completely avoided, both the protein fraction obtained from the extract and the raffinate can be measured at a concentration of more than 70 L after drying and milling for analysis. * The complete exclusion of oxygen and the use of antioxidants and / or reducing agents resulted in L values ​​of over 80 for both fractions. * It is also possible to achieve values ​​of 0.1 - 0.25 μm, which according to the prior art has not been shown before.

[0026] Extraction at reduced air pressure (vacuum) is advantageously carried out in such a way that the pressure in the gas phase of the closed extraction vessel is adjusted to less than 200 mbar, better still less than 100 mbar. In this case, the oxygen concentration in the water or in the extract should be considered as a target parameter. O 2 in the water utilized for the extraction or directly in the extract should be reduced to 0.5%. 2It is advantageous to try to reduce the concentration to values ​​below 7 mg / l (liter), advantageously below 3 mg / l, particularly advantageously below 0.5 mg / l or better still below 0.1 mg / l.

[0027] If it is not possible to reduce below these values ​​in a vacuum, it proves to be particularly advantageous in terms of the color or brightness of the protein preparation to remove dissolved oxygen substantially from the water used for the extraction by bubbling with high concentrations (more than 90% by volume) of nitrogen or argon and / or treatment with ultrasound, thereby reducing the oxygen concentration below the abovementioned values. In this case, advantageously, values ​​for dissolved oxygen below 0.1 mg / l, and in some cases even below 0.05 mg / l, can be achieved, which clearly limits the degree of discoloration.

[0028] Alternatively or additionally, it is advantageous to add ascorbic acid, citric acid, or another colorless, water-soluble antioxidant and / or reducing agent, such as sodium bisulfite, cysteine, etc., to the water used for extraction, thereby also suppressing the dark coloration and obtaining a lighter colored preparation. Whether the addition of antioxidant and / or reducing agent is sufficient to suppress oxidation or whether further measures as mentioned above are necessary to further reduce the oxygen concentration can be variably configured depending on the desired result. Moreover, it has surprisingly been found that the addition of reducing agents improves some functionalities of the preparation, such as its solubility and emulsification behavior.

[0029] To carry out the method, ideally the above mentioned methods are combined with one another to avoid oxidation. In this case, the oxygen proportion and oxidation potential in the extract can be reduced overall, so that it is no longer necessary to lower the pH value during the extraction below a value of 7 to avoid oxidation effects. Surprisingly, less than 1 mg of dissolved O per liter of extract is obtained. 2 At concentrations of 0.01g / ml, there was a clear decrease in the brightness of the dried and ground preparation (less than 70 L *The pH value can be increased to above 7.5 without having to accept a high pH value (up to 7.5), which allows a significant increase in the protein yield in the extract, since at higher pH values ​​a significantly higher proportion of the protein can be transferred to the extract phase.

[0030] By comparison, it is clear that if a pH value of 7.5 or higher is selected during extraction without the measures described, the color of the preparation becomes significantly darker. It has been shown that in an embodiment of the method according to the invention combining the above-mentioned measures, i.e. removing oxygen, for example by blowing in nitrogen (nitrogen content of more than 90% by volume) or argon, and adjusting the pH value in the extract to a value above 8.5, for example by adding 0.01 g to 1 g ascorbic acid and / or 0.01 g to 1 g cysteine ​​or cystine per liter of extraction water, it is still possible to obtain a light-colored protein preparation by subjecting the extract to ultrafiltration and / or diafiltration. A particularly light color can also be observed by reducing the pressure during extraction to a value below 50 mbar. In this case, in order to ensure that the protein fraction obtained from the extract is also color-wise storage-stable after drying, i.e. does not undergo graying or another type of dark discolouration during storage, the combination of a hypoxic or anoxic extract, the addition of antioxidants and / or reducing agents and the use of ultrafiltration and preferably also diafiltration of the extract has proven to be a particularly effective method combination.

[0031] It has been found that the prior treatment of the powder to reduce the air or oxygen content also brings about further advantages, especially when the dissolved oxygen has already been largely removed from the water used for the extraction.Thus, it has been found that sunflower powder treated by vacuum of less than 200 mbar, advantageously less than 50 mbar, or by blowing with nitrogen (or another gas suitable for this) before being introduced into the extraction, can give a lighter colored protein preparation than if the powder had not been previously freed of the air contained in its bulk.Preferably, it is desired to reduce the partial pressure of oxygen in the powder to less than 50 mbar, better still less than 20 mbar, particularly advantageously less than 10 mbar.

[0032] By completely or partially separating oxygen from the water before or during the extraction, where the process can be accelerated by warming the oxygen-containing water to a temperature above 20° C., preferably above 40° C., particularly preferably above 50° C., the pH value during the extraction process can be adjusted according to the invention to between 4 and 9. This can be determined by the oxygen content in the water, but can also be optimized with respect to the desired separation result. In the case of an oxygen content of more than 5 mg / l, the pH value is according to the invention below 6.5, preferably below 6. In the case of an oxygen content between 1 mg / l and 5 mg / l, the pH can be adjusted to a value up to 7.5, and below 0.1 mg / l a value up to 9 is possible.

[0033] However, this does not mean that below the oxygen values ​​mentioned above, the highest possible pH value should be selected in every case. Rather, low O values ​​of less than 0.1 mg / l should be selected in order to achieve certain properties, a defined protein composition or a particularly bright color. 2 The pH value can be adjusted and additionally antioxidants and / or reducing agents can be used, nevertheless a pH value of 6 can be selected. At pH 6 only albumin dissolves from the sunflower seeds, therefore it can be advantageous to adjust the pH to 6 to obtain only albumin.

[0034] In a particularly advantageous embodiment of the method, the adjustment of the pH is carried out by adding an antioxidant, such as ascorbic acid.

[0035] In the method according to the invention, the extraction is preferably carried out with a powder which has been ground to a defined particle size distribution before extraction and to which a certain amount of water has been added for the extraction. After the extraction, a separation between the raffinate and the extract is carried out. For a more complete extraction of the proteins, advantageously a further aqueous extraction is carried out with the raffinate. After at least one separation of the extract and the raffinate, the raffinate is subjected to drying and optionally to grinding in order to achieve an advantageous particle size distribution, as already further described above in the preferred grinding of the powder. From the extract, a proportion of sugars or other compounds with a correspondingly small molecular size is preferably removed, either by ultrafiltration or diafiltration (or both), or the protein is concentrated by precipitation, preferably at the isoelectric point of the protein and / or by ultrafiltration. The concentrated protein is subsequently adjusted to the above-mentioned particle size distribution, optionally by grinding, after it has been stabilized, for example by drying or freezing.

[0036] In this case, the protein preparation from the raffinate has a protein content of more than 25% by weight, preferably more than 40% by weight, particularly preferably more than 50% by weight, and a sugar content (monosaccharides, disaccharides combined) of less than 6% by weight, preferably less than 1% by weight, particularly preferably less than 0.5% by weight. Furthermore, the protein fraction obtained from the raffinate has a chlorogenic acid content of less than 1% by weight, preferably less than 0.5% by weight, particularly preferably less than 0.1% by weight.

[0037] The combination of such low chlorogenic acid concentrations of less than 0.1% by weight in the protein preparation obtained from the raffinate with a relatively high protein content, preferably above 50% by weight, has the advantage, compared to previously known shell-free powders with a similar protein content, that no discoloration occurs even when adjusted to neutral or alkaline pH values ​​in food or cosmetic applications or in pet food or when the product is stored for longer periods. Conventional powders according to the prior art do not allow such pH values ​​or long storage times to be selected without discoloration.

[0038] Thus, by using extraction conditions with reduced oxygen and minimal oxidation, it has surprisingly been possible to produce good quality, light-coloured preparations from the raffinate and at the same time to obtain extracts which, in particular by ultrafiltration and / or diafiltration and / or precipitation, give rise to neutral, light-coloured protein concentrates with a protein proportion of more than 75% by weight, or even protein isolates with a protein content of more than 90% by weight.

[0039] Here too, the advantages of the reduction of the oxygen proportion or the reduction of oxidation according to the invention are evident. If these measures are selected, the ultrafiltration of sugars and other compounds with low molecular weight, on the one hand, and of proteins with molecular weights above 1000 Da, on the other hand, is much more effective than otherwise. This is not possible with membrane separations unless the measures limiting oxidation according to the invention are selected. In the method according to the invention, it is also possible to use adsorbents in order to separate the interfering components from the extract more easily. Due to the poorly oxidizing environment, only a small amount of protein is deposited on the surface of the adsorbent.

[0040] From the deoiled powder having a dark color, which may have a shell content of up to nearly 10%, it is possible to obtain L of more than 70, advantageously more than 80. * It has been shown that very brightly colored protein preparations having the desired color can be obtained.

[0041] The proposed method comprises determining from the extract or at least one of the extracts the following characteristics: a protein content of more than 75% by weight, preferably more than 80% by weight, particularly preferably more than 90% by weight; L greater than 70, preferably greater than 80, particularly preferably greater than 90 * a * b * L from color space * A bright optical appearance having a value, an emulsifying capacity of more than 200 ml oil / g protein, preferably more than 400 ml oil / g protein, particularly preferably more than 500 ml oil / g protein; A protein solubility at pH 7 of more than 10% by weight, better still more than 30% by weight, particularly preferably more than 40% or 50% by weight, based on the protein content of the preparation; A particle size distribution having a D90 value (corresponding to the amount of particles below this size of 90%) preferably of less than 500 μm, advantageously less than 250 μm and particularly advantageously less than 100 μm; A preparation having the formula:

[0042] The residue has the following properties: a protein content of more than 25% by weight, preferably more than 40% by weight, particularly preferably more than 50% by weight; L greater than 70, preferably greater than 80, particularly preferably greater than 90 * a * b * L from color space * A bright optical appearance having a value, an emulsifying capacity of more than 250 ml oil / g protein, preferably more than 400 ml oil / g protein, particularly preferably more than 500 ml oil / g protein; a protein solubility at pH 7 of more than 5% by weight, better still more than 20% by weight, particularly preferably more than 30% by weight, based on the protein content of the preparation; Moisture binding greater than 1g per gram of dried raffinate; Preferably, a particle size distribution with a D90 value of less than 1000 μm, advantageously less than 500 μm, particularly advantageously less than 250 μm; a polyphenol content in the raffinate of preferably less than 1% by weight, more preferably less than 0.5% by weight, particularly preferably less than 0.1% by weight (measurement method: Weisz et al. 2009, Identification and quantification of phenolic compounds from sunflower (Helianthus annuus L.) kernels and shells by HPLC-DAD / ESI-MS, Food Chemistry, 115 (2), 758-765), a residual content of organic solvents of preferably less than 50 mg / kg, particularly preferably less than 10 mg / kg; A preparation having the formula:

[0043] In summary, the proposed method comprises the following method steps: 1) providing a protein-containing powder from deoiled sunflower seeds having a protein content of more than 35% by weight, an oil content (AOAC 963.15 Soxhlet method) of less than 8% by weight, advantageously less than 4% by weight, particularly advantageously less than 2% by weight, and a shell content of less than 10% by weight, advantageously less than 5% by weight, particularly advantageously less than 1% by weight or less than 0.1% by weight, preferably having a protein solubility at pH 6 of more than 15% by weight, advantageously more than 20% by weight, based on the protein content in the powder, and / or a protein solubility in water at pH 7 of more than 25% by weight, advantageously more than 30% by weight, particularly advantageously more than 35% by weight, based on the protein content in the powder; 2) a process step of extracting said powder with water in a pH range above 4, advantageously above 5, particularly advantageously above 6 but below 9; 3) a method step of reducing the oxygen concentration in the water beforehand or during the process to a value of less than 7 mg / l, preferably less than 2 mg / l, particularly preferably less than 0.5 mg / l or less than 0.1 mg / l, and / or the following steps: a. reducing the air pressure in the extraction vessel to less than 200 mbar, better still less than 100 mbar, and / or b. Driving off dissolved oxygen by adjusting the temperature of the water to be used for the extraction to a value above 20° C., preferably above 40° C., particularly preferably above 50° C.; and / or C. Nitrogen, CO 2 , argon or another inert gas having a concentration of more than 90% by volume, advantageously more than 99% by volume, by introducing it into the water used for the extraction, preferably warmed to above 20° C., or into the extract, or by blowing nitrogen, CO on the surface of the water / extract. 2 , argon or another inert gas is supplied to the water or the extract, thereby 2 In the case of nitrogen, the concentration is more than 10 mg / l, preferably more than 15 mg / l, particularly preferably more than 20 mg / l. 2 and / or d. Adding ingredients with antioxidant and / or reducing properties (e.g., citric acid, ascorbic acid, sulfites, cysteine, etc.) before or during extraction; and reducing the oxygen activity by one or more of the following method steps: 4) preferably a method step of adjusting the pH value in the water to a value between 3 and 7.5, advantageously between 5.5 and 6.5; 5) a process step of separating the solids and the extractables; 6) preferably the method step of repeating the above extraction process at a higher pH value, particularly advantageously a first extraction being carried out at a pH value between 5.5 and 7 and a second extraction being carried out at a pH value between 7.5 and 9; 7) A method step of concentrating the proteins in the extract, preferably by precipitation or ultrafiltration and / or diafiltration; 8) Optionally, the process steps of drying and optionally milling the extract and (optionally) the raffinate or enriched protein fraction to achieve a desired particle size distribution; will be implemented. EXAMPLES

[0044] implementation: Sunflower flour from dehulled seeds with a husk proportion of less than 1% by weight (protein proportion 55%; protein soluble 40%; oil content 2.5% by weight) is suspended in distilled water in a ratio of 1:10 (based on the dry matter of the flour). The water used for this was flushed / purged with nitrogen for 1 hour before use in order to expel the oxygen dissolved therein. Furthermore, before the addition of the powder, the pH value of the water was adjusted to 6 with ascorbic acid. After the powder was added to the water, the pH was readjusted to 6 and subsequently stirred at room temperature for 30 minutes.

[0045] After this pre-extraction was finished, the suspension was centrifuged for 10 min at 8570 g and 20° C. The centrifugation residue was extracted again as above at pH 6 (second pre-extraction) and centrifuged as above. These pre-extractions, among other things, remove undesirable phenolic components from the powder. The centrifugation residue was then suspended again in water in a ratio of 1:10 (based on the dry mass) and adjusted to a pH value of 8.5 with sodium hydroxide solution. The suspension was then stirred for 30 min at room temperature to extract the proteins. The water used for this was purged with nitrogen for 1 h before use.

[0046] After protein extraction was completed, the residue (raffinate) and the supernatant (extract) were separated by centrifugation (10 min, 20° C., 8570 g). The raffinate was stabilized by lyophilization, while the finally obtained extract was subjected to protein precipitation.

[0047] For protein precipitation, the pH value of the extract was adjusted to 6 with ascorbic acid and stirred at room temperature for 30 min. The precipitated proteins were subsequently obtained by centrifugation (10 min, 20° C., 8570 g). The protein curd thus obtained was lyophilized for stabilization.

[0048] Product: a) Protein products from the extract phase: Protein content: 85% Protein solubility (pH 7): 12% Emulsifying capacity: 230 mL (oil) / g L * Value (L * a * b color space): 80 b) Residual extract: Protein content: 40% Protein solubility (pH 7): 25% Water binding: 1.2 g / g Emulsifying capacity: 485 mL (oil) / g L * Value (L * a * b color space): 80 Polyphenol content: 0.2 mass%

Claims

1. A method for producing a protein preparation from sunflower seeds, comprising at least the following steps: From shelled and deoiled sunflower seeds a shell content of less than 10% by weight; An oil content of less than 8% by weight; A protein content of more than 35% by weight; providing a protein-containing powder having carrying out at least one or more extraction steps with water at a pH value of greater than 4 and less than 7 on said protein-containing powder, after which a liquid phase is obtained as the extract and a solid-rich phase is obtained as the raffinate; separating the extract and the raffinate; concentrating and / or drying the extract and drying the raffinate; where A method comprising reducing the oxygen concentration in the water to a value below 7 mg / l and / or adding a component having an antioxidant effect to the water to reduce its oxidative activity and / or adding a component having a reducing effect before and / or during the one or more extraction steps.

2. 2. The method of claim 1, wherein the protein-containing powder has a protein solubility in water at pH 6 of more than 15% by weight relative to the protein content in the powder and / or a protein solubility in water at pH 7 of more than 25% by weight.

3. 3. The method according to claim 1 or 2, characterized in that the extraction step or steps are carried out at a reduced air pressure of less than 200 hPa for the reduction of the oxygen concentration in the water.

4. 4. The method according to claim 1, characterized in that nitrogen, carbon dioxide, argon or another inert gas having a concentration of more than 90% by volume is bubbled into or contacted with the surface of the water before and / or during the extraction step or steps, for reducing the oxygen concentration in the water.

5. 5. The method according to claim 1, wherein the oxygen concentration in the water is reduced by treatment with ultrasound.

6. 6. The method according to claim 1, characterized in that the temperature of the water is adjusted to a value above 20° C. for the reduction of the oxygen concentration in the water.

7. 7. The method according to any one of claims 1 to 6, characterized in that prior to the extraction step or steps, the oxygen content of the protein-containing powder is reduced by vacuum or by bubbling with carbon dioxide or an inert gas.

8. 8. The method according to claim 7, characterized in that the reduction of the oxygen content of the protein-containing powder is carried out until the partial pressure of oxygen in the protein-containing powder is less than 50 hPa.

9. 9. The method according to any one of claims 1 to 8, characterized in that the extraction step or at least one of the extraction steps is carried out at a pH value below 8.

10. 10. The method according to any one of claims 1 to 9, characterized in that the concentration of the separated extract is carried out by ultrafiltration and / or diafiltration and / or precipitation.

11. 11. The method according to any one of claims 1 to 10, characterized in that the powder is subjected to multiple extraction steps with water, wherein at least one of the extraction steps is carried out at a pH value between 5.5 and 7, and subsequently the others of the extraction steps are carried out at a pH value between 7.5 and 9.

12. 12. The method according to any one of claims 1 to 11, characterized in that the protein-containing powder is milled before the extraction step to obtain a particle size distribution in which 90% of the particles have a particle size below 100 μm by mass.

13. 12. The method according to any one of claims 1 to 11, characterized in that the protein-containing powder is milled before the extraction step to obtain a particle size distribution in which 90% of the mass fraction of the particles has a particle size between 100 μm and 2500 μm.

14. 14. The method according to claim 1, wherein the provided protein-containing powder has a residual content of the solvent used during deoiling, said residual content being in the range between 0.001% and 0.4% by weight.