WO2003070267A1 - Enhancing the availability of minerals by using biologically active peptides - Google Patents

Enhancing the availability of minerals by using biologically active peptides Download PDF

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Publication number
WO2003070267A1
WO2003070267A1 PCT/FI2002/001051 FI0201051W WO03070267A1 WO 2003070267 A1 WO2003070267 A1 WO 2003070267A1 FI 0201051 W FI0201051 W FI 0201051W WO 03070267 A1 WO03070267 A1 WO 03070267A1
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Prior art keywords
product
casein
minerals
availability
enhancing
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PCT/FI2002/001051
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English (en)
French (fr)
Inventor
Mirkka Narva
Riitta Korpela
Olli Tossavainen
Annika Mäyrä-Mäkinen
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Valio Ltd
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Priority to JP2003569223A priority Critical patent/JP4242293B2/ja
Priority to EP02788013A priority patent/EP1485119A1/en
Priority to AU2002352303A priority patent/AU2002352303A1/en
Publication of WO2003070267A1 publication Critical patent/WO2003070267A1/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • C07K14/4701Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
    • C07K14/4732Casein
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23CDAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING THEREOF
    • A23C9/00Milk preparations; Milk powder or milk powder preparations
    • A23C9/12Fermented milk preparations; Treatment using microorganisms or enzymes
    • A23C9/13Fermented milk preparations; Treatment using microorganisms or enzymes using additives
    • A23C9/1307Milk products or derivatives; Fruit or vegetable juices; Sugars, sugar alcohols, sweeteners; Oligosaccharides; Organic acids or salts thereof or acidifying agents; Flavours, dyes or pigments; Inert or aerosol gases; Carbonation methods
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/17Amino acids, peptides or proteins
    • A23L33/18Peptides; Protein hydrolysates
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/17Amino acids, peptides or proteins
    • A23L33/19Dairy proteins
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/1703Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • A61K38/1709Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis

Definitions

  • the invention relates to enhancing the availability of minerals and to strengthening the skeletal system by using biologically active peptides and products containing them.
  • Peptides and products containing them are useful for instance in preventing and treating different disorders and illnesses related to bone mineral absorption.
  • a product having a high short-chain peptide content and a high calcium content has been found especially effective for use in accordance with the invention.
  • Proteins in food provide the source of essential amino acids and nitrogen for the organ system.
  • the proteins in food contain peptides that may be significant regulators of the functions of the organ system.
  • Biologically active peptides can for instance affect the absorption of nutri- ents (phosphopeptides and casomorphines), the secretion of hormones (casomorphines) and the immunity (immunopeptides, casokinins, casomorphines).
  • Casein in milk is the most significant source of biologically active peptides in food (Schlimme E. & Meisel H. Biologically active peptides derived from milk proteins. Structural, physiological and analytical aspects. Die Nah- rung 1995; 39:1-20; Steijns J. Dietary proteins as the source of new health promoting biologically active peptides with special attention to glutamine peptide. Food Tech Europe 1996; March/April: 80-84).
  • Phosphopeptides have been found to affect the absorption of minerals in the body. Phosphopeptides are mainly formed from ⁇ and ⁇ ca- spurs through trypsin-caused proteolysis. Lee with his research group has observed that a diet containing 200 g/kg of casein increased the formation of phosphopeptides (Lee Y et al. Phosphopeptides and soluble calcium in small intestine of rats given a casein diet. Br J Nutr 1980; 43:457-67). When casein was the only source of food, phosphopeptides were, however, not formed. The scientists concluded that the formation of phosphopeptides requires not only casein but also other sources of food, such as starch or fat. This could be due to the fact that other nutrients increase the activity of proteolytic enzymes in the small intestine.
  • Casein phosphopeptides improve zinc and calcium absorption from rice-based but not from whole-grain infant cereal. J Pediatr Gastrolog Nutr 1997; 24:56-62). Heaney et al. gave 35 healthy women 250 g of labelled calcium and 87.5 mg of phosphopeptides or placebo with their food. Calcium absorption was significantly improved in the women who received phosphopeptides and whose calcium absorption was otherwise weak. In the women whose calcium absorption was high and those receiving placebo, phosphopeptides did not markedly increase calcium absorp- tion (Heaney RP et al. Effect of caseinophosphopeptide on absorbability of coingested calcium in normal postmenopausal women. J Bone Miner Metab 1994; 12:77-81 ).
  • phosphopeptides could be beneficial for instance to babies, the elderly, and in illnesses, in which the absorption of minerals, es- pecially calcium, is impaired or the need for them is increased. Adding phosphopeptides to foodstuffs could be a safe way to increase calcium absorption (Hansen M. et al. 1997, ibid.).
  • Biologically active peptides also include peptides affecting blood pressure.
  • ACE i.e. the enzyme converting angiotensin I
  • ACE inhibitors can prevent this action and thus act as agents lowering blood pressure.
  • Peptides serving as ACE inhibitors are present in milk casein and fish and corn proteins (Schlimme et al. 1995, ibid.).
  • Blood-pressure affecting peptides disclosed in the literature of the art include, for instance: Asp-Glu-Leu-Gln-Asp-Lys-lle-His-Pro-Phe-Ala-Gln- Thr-Gln-Ser-Leu-Val-Tyr-Pro-Phe-Gly-Pro-lle-Pro-Asn-Ser and Leu-Leu-Tyr- Gln-Gln-Pro-Val-Leu-Gly-Val-Arg-Gly-Pro-Phe-Pro-lle-lle-Val (Yamamoto N et al.
  • Sour milk products are also reported to contain peptides with a blood-pressure lowering effect. It is assumed that the peptides are formed in the milk products as a result of hydrolysis by lactic acid bacteria and especially hydrolysis of milk proteins caused by their extracellular proteinases.
  • Yamamoto et al. describe the purification and characterization of the proteinase originating from the micro-organism Lactobacillus helve- ticus CP790 in publication J. Biochem. 114 (1993) 740. Yamamoto et al. have also reported a study in which s ⁇ and ⁇ caseins were hydrolysed with said proteinase and the obtained peptides were examined with respect to their ACE-inhibiting effect (J Dairy Sci 1994; ibid.). A total of 25 peptides were examined and they were very different in molecular size and effect. The most effective peptides were three peptides obtained from ⁇ casein and containing 8, 18 and 27 amino acids, respectively.
  • ACE activity of milk fermented with Lactobacillus helveticus strain CP790 and its variant CP791 that is deficient with respect to its proteinase activity were also compared, and the former was found effective in SHR rats developing spontaneous high blood pressure, but not in ordinary rats, whereas the latter lacked any activity.
  • Nakamura et al. describe the use of a souring agent containing Lactobacillus helveticus and Saccharomyces cerevisiae in the preparation of two ACE inhibitors in publication J Dairy Sci 1995; 78:777 - 783. Skimmed milk was fermented with said souring agent, after which the ACE inhibitors were purified chromatographically and analysed. Both active compounds were tripeptides, Val-Pro-Pro and lle-Pro-Pro.
  • US patent 5,449,661 Nakamura et al., describes the preparation of a peptide containing the tripeptide sequence Val-Pro-Pro and its use in lowering high blood pressure.
  • the peptide is prepared by fermenting skimmed milk powder with Lactobacillus helveticus strain JCM-1004, after which the peptide is purified chromatographically and freeze-dried.
  • Peptides acting as ACE inhibitors have been estimated to possibly have an effect on immunity based on the fact that bradykinins, which are stimulated by ACE inhibitors, are capable of increasing the activity of macrophages and lymphocytes (Migliore-SAMP D et al. Biologically active milk peptides implicated in immunomodulation. J Dairy Res 1989; 56:357-362). The effect of these peptides on mineral absorption has not been studied or described in the literature of the art. [0014] Injuries and illnesses related to the weak mineral level of bone are becoming commoner all the time. They are present in all age groups.
  • a second risk group comprises persons with an increased need of calcium, such as young girls and breast-feeding and pregnant women.
  • magnesium transmits muscle and nerve impulses and serves as building material for bones and teeth.
  • Magnesium has also been found to improve immune response. Magnesium deficiency is rare, but dehydration may lead to magnesium depletion.
  • One of the tasks of potassium is to control fluid balance and contract muscles. Potassium deficiency may cause muscle weakness.
  • the intake of magnesium and potassium is important in illnesses that involve disturbances in fluid balance or dehydration, and for athletes to recover after performance.
  • the product to be used according to the invention has a high content of peptides enhancing the availability of minerals.
  • the product also has an optimised salt content, which means that the number of monovalent cations is low and the number of beneficial bivalent cations is high in comparison with a known product of corresponding type.
  • a most preferred embodiment makes available a product that has a high content of peptides enhancing the availability of minerals and a high calcium content.
  • a yet further object of the present invention is to provide a method for enhancing the availability of minerals and/or for strengthening bones by administering to an individual in need of such treatment peptides enhancing the availability of minerals or a product containing them in a sufficient amount to produce the desired effect.
  • a yet further object of the present invention is to provide a method for the prevention, alleviation or cure of osteoporosis by administering to an individual in need of such treatment peptides enhancing the availability of minerals or a product containing them in a sufficient amount to produce the desired effect.
  • a yet further object of the present invention is to provide a method for enhancing the availability of calcium by administering to an individual a product that has a high content of casein-derived, small-molecular peptides and a high calcium content and that has been prepared by fermenting a casein-containing starting material with Lactobacillus helveticus strain LBK- 16H, DSM 13137, optionally removing partly or entirely casein and/or other milk proteins and/or lactose, in a sufficient amount to produce the desired effect.
  • the fermented product is also subjected to nanofiltration.
  • Figure 1 shows the effect of a product to be used according to the invention and that of various reference samples on the bone density of a rat.
  • Figure 2 shows the effect of a product to be used according to the invention and that of various reference samples on the bone mineral content of a rat.
  • FIG. 3 shows the effect of different concentrations of VPP (Val-Pro-Pro) used according to the invention on bone formation.
  • Figure 5 shows the effect of a product to be used according to the invention and that of a reference sample on parathyroid hormone (PTH) concentration.
  • Figure 6 shows the effect of a product to be used according to the invention and that of a reference sample on serum calcium concentration.
  • peptides enhancing the availability of minerals or a product containing them Di-, tri- and tetrapeptides and their mix- tures are above all considered peptides enhancing the availability of minerals.
  • These peptides can advantageously be prepared from casein or casein- containing starting material by fermentation. Especially preferable is to use a method, in which a product containing biologically active peptides is formed by fermentation, after which it is concentrated and the composition is finished off by nanofiltration.
  • the preferred embodiment provides excellent possibilities to use starting materials of different type and to modify the composition of the end product as desired, as described in detail in the following.
  • the invention thus relates to the use of casein-derived, small-molecular peptides in the preparation of a product enhancing the avail- ability of minerals.
  • the invention further relates to the use of a product having a high content of casein-derived, small-molecular peptides in the preparation of a product enhancing the availability of minerals.
  • the casein-derived, small-molecular peptides comprise di-, tri-, and tetrapeptides and their mixtures.
  • the IPP, VPP and calcium contents are high.
  • the invention further relates to the use of a product having a high content of casein-derived, small-molecular peptides and a high calcium content that has been prepared by fermenting casein-derived starting material with a lactic acid bacterium, and possibly by nanofiltration of the fermented peptide-containing product obtained, in the preparation of an end product enhancing the availability of minerals.
  • the invention relates to the use of a soured composition that contains casein-derived peptides, minerals and living lactic acid bacterium, in the preparation of a product enhancing the availability of minerals.
  • the invention also relates to a method for enhancing the availability of minerals and/or for strengthening bones by administering to an individual peptides enhancing the availability of minerals or a product contain- ing them in a sufficient amount to produce the desired effect.
  • the individual is primarily human.
  • the positive effects of the products used in accordance with the invention are naturally also beneficial to animals, especially pets and production animals. Examples of these include dogs, cats, rabbits, horses, cows, pigs, goats, sheep and poultry.
  • enhancing the availability of minerals refers to a complex effect that comprises especially the absorption and effect of minerals on bone cells.
  • Biologically active peptides for use in enhancing the availability of minerals in accordance with the present invention can thus be formed by fermentation.
  • the starting material in fermentation can be any product that contains the sequences of the desired biologically active peptides as part of its own peptide or protein sequence.
  • Milk protein, especially casein is preferably used as such or in the form of different preparations.
  • Suitable starting materials include preferably also various casein-containing milk products, such as skimmed milk or milk with varying fat contents as such or in the form of a corresponding milk powder and sour milk products, such as sour milk, buttermilk, yoghurt, curdled milk, unripened cheese, etc.
  • Fermentation can be carried out with any lactic acid bacterium that is capable of producing small-molecular peptides enhancing the availability of minerals from the starting material.
  • Suitable lactic acid bacteria can be found among species belonging to the Lactobacillus, Lactococcus, Leuconostoc, Streptococcus and Bifidobacterium genera, for instance.
  • the most proteolytic of the lactic acid bacteria is Lactobacillus helveticus and it is thus considered especially suitable for this purpose.
  • a preferable Lactobacillus helveticus strain is L. helveticus LBK-16H, DSM 13137, which is described in detail in patent publication WO 01/32836.
  • the lactic acid bacteria can be used as pure cultures or mixed cultures, separately or together the conventionally used and commercially available souring agents.
  • the lactic acid bacteria can also be used together with other micro-organisms. Microbe combinations are appropriately selected to achieve the best possible taste for the end product and to prevent the risk of contamination.
  • the fermentation conditions are selected to meet the requirements of the used strain so as to form a sufficient amount of biologically active peptides to produce the desired effect.
  • suitable condi- tions such as temperature, pH and aeration, is part of the know-how of a person skilled in the art.
  • the temperature can be 30 to 45°C, for instance.
  • the fermentation is allowed to continue until the desired amount of biologically active peptides has formed. Normally, this takes approximately 20 to 30 hours, preferably 22 to 24 hours.
  • VPP Val-Pro-Pro
  • IPP lle-Pro-Pro
  • the cell suspension is recovered. It can be used as such or the peptides can be separated and purified using conventional methods.
  • the cell suspension can also be concentrated, for instance by evaporating or drying it partly or completely, such as spreading it on a plate, drying and finally grinding it to produce a well-preserving dry powder.
  • the fermented product may be subject to pre-treatment, for instance to remove casein or all milk proteins from it, before nanofiltration.
  • Methods suited for pre-treatment are known in the art and comprise various precipitation and filtering methods, for instance.
  • One useful method comprises the adjustment of the pH of the fermented product to an area, in which casein precipitates, for instance to approximately 4.6 at 37°C, after which the precipitated casein is separated using a curd separator, casein separation sieve, decanter, by sedimentation or some other suitable method.
  • a second method comprises ultrafiltration of the soured product at pH 3 to 3.5, whereby all proteins are retained on the membrane and nearly protein-free whey is obtained as the permeate.
  • Coprecipitation producing nearly protein-free, peptide-containing whey can be achieved by CaCI 2 addition, thermal treatment or acid addition, for instance. If necessary, possible casein dust is removed by centrifugation. Other agents, such as lactose, can also be removed prior to nanofiltration for instance by enzyme hydrolysis or fermentation.
  • the nanofiltration membrane can be a conventional NF membrane, such as Nanomax-50 (Millipore) or Desal 5 (Desal
  • Nanofiltration is performed up to a desired dry content or volume concentration ratio, which is usually as high as possible.
  • the dry content is in the range of 20 to 40% and the volume concentration ratio is approximately 5 to 20.
  • the (whey) concentrate can be diluted with water, whereby a larger amount of salts and lactic acid can be removed from the con- centrate during nanofiltration. This is a simple and efficient way of adjusting the amount of salts in the concentrate to a desired level.
  • the small peptides enhancing the availability of minerals and formed during fermentation are completely retained by the nanofiltration membrane.
  • the nanofiltra- tion method also provides the possibility of removing lactose entirely; lactose can be degraded enzymatically before the nanofiltration step, whereby mono- saccharides are removed to a large extent.
  • lactic acid, small nitrogen compounds, such as urea, and monovalent salts permeate the membrane.
  • the peptide content of the product in- creases.
  • bivalent ions especially the desired calcium and magnesium ions
  • monovalent ions such as sodium, potassium and chloride ions
  • Sodium ions are known to have a significant effect on the fluid balance of the body, and a decrease in the number of these harmful ions can thus be taken as a significant advantage.
  • Certain bivalent ions, especially calcium ions are known to improve the mineralization of bone, for instance, and thus a high content of them is considered highly desirable.
  • the content of certain selected minerals in the product can also be increased by adding the desired mineral in the form of a suitable salt, for instance.
  • suitable salt for instance.
  • Such minerals include calcium and magnesium in particular.
  • Table 1 shows the behaviour of the components contained in the prepreparation formed during the fermentation step of the above two-step method based on fermentation and nanofiltration in the nanofiltration step.
  • the used exemplary composition is formed by fermenting skimmed milk with a Lac- tobacillus helveticus strain.
  • other products can also be used as starting materials.
  • the fermentation conditions, the optional nanofiltration treatment and possible other pre- treatments and additional treatments affect the outcome, so the composition of the end products (and the nanofiltration results) naturally change and may differ from what is stated herein.
  • the product prepared as described in example 2 of this pub- lication has been found to be extremely suitable for the purpose of the invention.
  • the total composition of the product has been found optimal in the conducted comparative tests.
  • Many factors influence the physiological activities of the product; for instance the extended proteolysis of the product that provides a selection of different active peptides, the excellent mineral content of the product, the living microbe cells in the product and the acidity of the product. All these properties can be influenced and they can be maximized by changing the different parameters of the preparation method in an appropriate manner.
  • the proteolysis conditions such as enzyme activity and reaction time, affect the quality and amount of obtained peptides. It is also possible to influence these by nanofiltration, and especially to raise the peptide content of the product significantly.
  • the salt contents and their ratios can easily be adjusted to the desired level.
  • the content of the desired bivalent ions, in particu- lar, can be increased and the content of monovalent ions decreased.
  • the acidity and the number and type of microbe cells can also easily be maximized in manners know to a person skilled in the art.
  • the products described above can be used as such to achieve the desired effect.
  • the products can also be dried and used in the form of a powder or lyophilized preparation.
  • the products can also preferably be used in the preparation of functional foodstuffs or other products.
  • the concept 'foodstuff' has a wide meaning in this publication, covering all consumable products that can be in a solid, jellied or liquid form, and covering both ready-made products and products to which the bio- logically active peptides or a product containing them are added during consumption as an additive or part of the product.
  • Foodstuffs can be products of dairy industry, meat processing industry, prepared food industry, beverage industry, bakery industry and confectionery industry, for instance. Typical products include milk products, such as yoghurt, curdled milk, curd, sour milk, but- termilk, other sour milk products, unripened cheeses and ripened cheeses, fillings of snack bars, etc.
  • a second important group includes beverages, such as whey beverages, fruit beverages, and beers.
  • the biologically active peptides or a product containing them are used in a sufficient amount to achieve the de- sired effect enhancing the absorption of minerals.
  • the amount to use depends mainly on the concentration degree of the whey and is for instance 0.1 to 30%, preferably approximately 5 to 15% as calculated from the weight of the end product.
  • Biologically active peptides or a product containing them can be added to a food product during its preparation or to a finished food product.
  • the food products in question thus contain peptides enhancing the availability of minerals, or a product containing them, in addition to other components contained in corresponding food products and fully correspond in taste and behav- iour with these conventional products.
  • the invention will be described in greater detail by means of the following examples. These examples are provided only to illustrate the invention and should not be considered to restrict its scope of protection in any way.
  • the product marked with X in the reference examples and figures is prepared according to examples 2 and 5.
  • the proteolysis degree and mineral content of different products [0063] To determine the proteolysis degree of different sour milk products, their protein content (protein), total nitrogen content (Tot.N), non- protein nitrogen content (NPN; urea, amino acids, small peptides, etc.), amount of titrated free amino acids (Titr.f.aa) and pH were determined.
  • the proteolysis degree can be roughly determined by calculating the ratio of non- protein nitrogen to total nitrogen (NPN / Tot.N); the amount of titrated free amino acids mmol/g protein is obtained by calculating Titr.aa/Prot.
  • the product of the invention Evolus beverage (80% sour milk base) with added peptide concentrate, NPN / Tot.n then does not show the proteolysis degree
  • the study determined the effect of water, milk, sour milk and two IPP and VPP peptide-containing beverages, the Japanese commercial Calpis sour milk product, Calpis Food Industry Company Ltd, and product X (Evolus, Valio Oy) of example 2 on the skeletal system.
  • Six-week old SH rats were used in the study and were given one of the test beverages ad libitum for 14 weeks. After this, the bones of the rats were removed and the bone mineral densities (BMD) and bone mineral content (BMC) were determined with Dexa (dual energy X-ray absorptiometry). Dexa is a technique based on low-energy x-rays that measures bone density.
  • Fl application 992360 describes the preparation of a corresponding Evolus product and its activity as a blood-pressure lowering agent. As described in the publication, the first studies were made on rats, after which they were repeated on humans. In terms of blood pressure, both studies showed corresponding, clear results. Therefore, there is no reason to believe that the currently on-going further studies concerning the absorption of minerals in humans would not produce similar results as in the animal tests described above. Table 4
  • the object of the study was to determine the active factor responsible for the result obtained in reference example 2.
  • the peptide fraction of a milk product soured with L. helveticus the peptide fraction of Neo sour milk (Valio Oy, Helsinki, Finland), and pure peptides formed with L. helveticus, IPP (isoleucine-proline-proline) and VPP (valine-proline-proline), were added to bone forming cells. Bone formation was measured by the amount of calcium accumulated during the test. The mean amount of calcium released in the baseline group was given the value 100%.
  • Baseline (BL, negative control) and BMP-4 (C, bone morphogenetic protein 4), which is an agent increasing bone formation, were used a controls in the test.
  • * (p ⁇ 0.05), ** (p ⁇ 0.01 ) and *** (p ⁇ 0.001 ) represent statistically significant differences from baseline.
  • the results show clearly that pure peptides markedly increase bone formation.
  • helveticus had a small effect on bone formation, * (p ⁇ 0.05) with 10 "5 and 10 "3 diluted whey from sour milk acidified with Lactobacillus helveticus, ** (p ⁇ 0.01 ) with 10 "4 diluted whey.
  • This effect can be explained by the IPP and VPP con- tent of the peptide fraction.
  • the fraction of Neo sour milk had no effect on bone formation.
  • Lactobacillus helveticus strain LBK 16-H was grown in MRS broth at 37°C for 24 hours and inoculated into reconstituted milk (10%) to form an inoculum. After two growth cycles, the inoculum (15%) was inoculated into a fermentor medium made up of 9 to 10% skimmed milk powder milk and sterilized at 110° for 10 minutes. The fermentation was performed at 37°C for 22 to 24 hours under continuous strong agitation. The product can be used as such, in a dry and/or ground form, or the desired peptides can be separated from it using methods known per se.
  • Example 2 The preparation of a product to be used according to the invention
  • a product soured according to example 1 was nanofiltrated as follows.
  • composition Concentrate Dry powder
  • Removed casein contains a great deal of whey that contains as much biologically active peptides as fermented sour milk.
  • the casein was used as such in the curd, to which biologically active peptides were added in this manner.
  • Lactobacillus helveticus strain LBK 16-H was grown in MRS broth at 37°C for 24 hours to form an inoculum, as described in example 1.
  • the inoculum was inoculated into a fermentor medium that was made up of an aqueous solution of acid precipitated casein (2.8%) and glucose (2.5%).
  • Casein was dissolved by raising the pH to 6.7 with 10% KOH. Culturing was performed at 37°C for 24 hours.
  • Corresponding amounts of biologically active peptides VPP and IPP as when fermenting milk were produced in the product, but separating the peptides from the casein solution was easier than from milk.
  • Sour milk containing peptides that enhance the absorption of minerals was prepared by adding 3.5% of a peptide concentrate obtained according to example 1 to a commercially available sour milk.
  • the composition of the resulting product is shown in Table 6 that also shows for comparison the composition of a second commercially available sour milk product, AB sour milk, Valio Oy.
  • Table 6 The composition of an Evolus product and a commercial sour milk product

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PCT/FI2002/001051 2002-02-25 2002-12-20 Enhancing the availability of minerals by using biologically active peptides WO2003070267A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP2003569223A JP4242293B2 (ja) 2002-02-25 2002-12-20 骨の強化および骨形成を増加させるための組成物
EP02788013A EP1485119A1 (en) 2002-02-25 2002-12-20 Enhancing the availability of minerals by using biologically active peptides
AU2002352303A AU2002352303A1 (en) 2002-02-25 2002-12-20 Enhancing the availability of minerals by using biologically active peptides

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FI20020360 2002-02-25
FI20020360A FI112031B (fi) 2002-02-25 2002-02-25 Biologisesti aktiivisen tuotteen uusi käyttö

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EP (1) EP1485119A1 (zh)
JP (1) JP4242293B2 (zh)
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FI (1) FI112031B (zh)
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007132054A1 (en) 2006-05-15 2007-11-22 Valio Ltd New use of therapeutically useful peptides
JPWO2006004105A1 (ja) * 2004-07-05 2008-04-24 カルピス株式会社 ペプチド混合物の製造法、抗高血圧ペプチド含有発酵乳の製造法及び抗高血圧ペプチド製剤の製造法
JP2009532018A (ja) * 2006-02-20 2009-09-10 コンパニ・ジェルベ・ダノン ヘルベティカス乳酸桿菌の新規株
CN103221531A (zh) * 2010-11-09 2013-07-24 可尔必思株式会社 具有高蛋白质水解活性的瑞士乳杆菌细菌

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FI122531B (fi) * 2009-09-30 2012-03-15 Valio Oy Juusto ja menetelmä sen valmistamiseksi

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPWO2006004105A1 (ja) * 2004-07-05 2008-04-24 カルピス株式会社 ペプチド混合物の製造法、抗高血圧ペプチド含有発酵乳の製造法及び抗高血圧ペプチド製剤の製造法
JP4723501B2 (ja) * 2004-07-05 2011-07-13 カルピス株式会社 ペプチド混合物の製造法、抗高血圧ペプチド含有発酵乳の製造法及び抗高血圧ペプチド製剤の製造法
JP2009532018A (ja) * 2006-02-20 2009-09-10 コンパニ・ジェルベ・ダノン ヘルベティカス乳酸桿菌の新規株
WO2007132054A1 (en) 2006-05-15 2007-11-22 Valio Ltd New use of therapeutically useful peptides
CN103221531A (zh) * 2010-11-09 2013-07-24 可尔必思株式会社 具有高蛋白质水解活性的瑞士乳杆菌细菌
CN103221531B (zh) * 2010-11-09 2018-03-16 朝日集团控股株式会社 具有高蛋白质水解活性的瑞士乳杆菌

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EP1485119A1 (en) 2004-12-15
JP2005517424A (ja) 2005-06-16
FI20020360A0 (fi) 2002-02-25
JP4242293B2 (ja) 2009-03-25
FI112031B (fi) 2003-10-31
AU2002352303A1 (en) 2003-09-09
RU2004128448A (ru) 2005-04-20

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