JP5132076B2 - Digestive enzyme reaction inhibitor / retarder - Google Patents

Description

  The present invention relates to a digestive enzyme reaction inhibitor / retarder.

  In developed countries, excessive intake of lipids and proteins has been pointed out in recent years, and obesity and lifestyle-related diseases that are thought to be caused by excess energy are increasing.

  In this situation, dietary fiber is not degraded by human digestive enzymes, and at the same time, it is said that it has the effect of suppressing and delaying digestion and absorption of ingested nutrients such as lipids and proteins that are eaten, thereby suppressing excess energy. And prevention of lifestyle-related diseases. Furthermore, dietary fiber has physiological effects such as lowering cholesterol and improving bowel movement, and its intake has been promoted, but its intake is still insufficient.

  On the other hand, polysaccharides such as glucomannan, locust bean gum, and guar gum extracted and separated from plant rhizomes and seeds have functions such as emulsifying properties, thickening properties, gelling properties, and stability. Widely used in the food industry for the purpose of improving texture. Since these polysaccharides are not decomposed by human digestive enzymes and have physiological effects equivalent to the above dietary fiber, they have been used as a dietary fiber source in recent years.

  Since these polysaccharides exhibit high viscosity in water, even when added in a small amount, the physical properties and texture of food may be greatly changed, which may lead to a decrease in palatability. Therefore, it is difficult to add such a large amount as to obtain a physiological effect as dietary fiber, and in order to avoid this problem, products having been decomposed with an enzyme to have a low viscosity (low molecular weight) have been developed.

On the other hand, it is known that the effect of polysaccharides on inhibiting and delaying digestion and absorption of ingested nutrients such as lipids and proteins is related to the viscosity of polysaccharides (Non-Patent Document 1). Polysaccharides with low molecular weight were thought to have a low effect of inhibiting or delaying digestive enzyme reaction and preventing excessive absorption of nutrients, even though physiological effects as dietary fiber were obtained.
G. Isaksson et al., “Effect of Dietary Fiber on Pancreatic Enzyme Action, and Time of Incubation”, Gastroenterology 82: 918-24, 1998

  An object of the present invention is to provide a digestive enzyme reaction inhibitor / retarder containing a polysaccharide with an average molecular weight adjusted.

  The present inventors have repeated experimental studies on rheology, prepared various polysaccharide aqueous solutions to achieve the same viscosity using zero shear viscosity as an index, added it to a substrate such as separated soy protein, and digested it from the decomposition curve of the substrate. The reaction was measured. As a result of analysis of measurement results focusing on dynamic viscoelastic parameters such as complex viscosity and storage elastic modulus, polysaccharides with specific molecular properties can be a substrate by digestive enzymes without greatly changing the physical properties of the system. It has been found that the digestive reaction of can be effectively suppressed / retarded. The present inventors have studied the digestion reaction inhibiting / retarding effect using polysaccharide aqueous solutions having various average molecular weights and molar numbers of molecules, and have completed the present invention.

Accordingly, the present invention provides the digestive enzyme reaction inhibitor / retarder described in the following section:
Item 1. A digestive enzyme reaction inhibitor / retarder containing a polysaccharide;
The dynamic viscoelasticity of the 1 wt% polysaccharide aqueous solution was measured at 20 ° C. using a dynamic viscoelasticity measuring device ARES (manufactured by Rheometric Scientific) equipped with a cone-plate jig having a diameter of 50 mm. When
(a) G ″> G ′ in the frequency range of 0.1 to 100 rad / s, and
(b) Complex viscosity η ^* = (G ′ ² + G ″ ² ) ^1/2 / ω indicates a Newtonian equilibrium, and η ^* is less than 1 Pa · s. Retarder:
Where G ′, G ″, w denote storage modulus, loss modulus, and frequency, respectively;
Item 2. The digestive enzyme reaction suppression / retarding agent according to Item 1, wherein the average molecular weight of the polysaccharide is 2.0 × 10 ⁶ g / mol or less as a weight average molecular weight when measured by a static light scattering method;
Item 3. A digestive enzyme reaction inhibitor / retarder used together with a digestive enzyme substrate, wherein the ratio of the polysaccharide contained in the reaction inhibitor / retarder is 0.5 to 100 mmol per mole of digestive enzyme substrate, Item 1 or 2 digestive enzyme reaction inhibitor / retarder;
Item 4. Item 4. The digestive enzyme reaction inhibitor / retardant according to any one of Items 1 to 3, wherein the polysaccharide is at least one selected from the group consisting of glucomannan, locust bean gum, and guar gum;
Item 5. Item 5. The digestive enzyme reaction inhibitor / retarder according to Item 4, wherein the polysaccharide is guar gum;
Item 6. The digestive enzyme reaction inhibitory / retarding agent according to any one of Items 1 to 5, wherein the digestive enzyme substrate is a protein;
Item 7. Item 7. The digestive enzyme reaction suppressing / retarding agent according to any one of Items 1 to 6, wherein the digestive enzyme is a proteolytic enzyme.

  The digestive enzyme reaction inhibitor / retarder of the present invention effectively suppresses / retards the digestive enzyme reaction of a substrate such as a protein without greatly changing the physical properties of the system, thereby rapidly absorbing and over-absorbing nutrients in the body. Can be prevented.

  Hereinafter, the present invention will be described in detail.

Digestive enzyme reaction inhibitor / retarder In the present invention, the digestive enzyme reaction suppressor / retarder refers to a composition for inhibiting / delaying a digestion reaction of a substrate such as a protein by digestive enzymes in the body.

  The digestive enzyme reaction inhibitor / retarder of the present invention is characterized by containing a polysaccharide.

The polysaccharide contained in the digestive enzyme reaction inhibition / retarding agent of the present invention is a dynamic viscoelasticity measuring apparatus ARES (reo) having a cone-plate jig having a diameter of 50 mm. Using metric scientific) at 20 ° C,
(a) G ″> G ′ in the frequency (angular velocity) range of 0.1 to 100 rad / s, and
(b) Complex viscosity η ^* = (G ′ ² + G ″ ² ) ^1/2 / ω represents a Newtonian equilibrium, and η ^* at that time is less than 1 Pa · s.

  Here, G ′, G ″, and ω represent storage elastic modulus, loss elastic modulus, and frequency (angular velocity), respectively. The polysaccharide contained in the digestive enzyme reaction inhibitor / retarder of the present invention is characterized in that loss tangent tan δ = G ″ / G ′> 1 when dynamic viscoelasticity is measured under the above conditions.

In the present invention, the fact that the complex viscosity η ^* indicates Newtonian equilibrium in the range of 0.1 to 100 rad / s means that there exists a frequency region that exhibits the behavior of Newtonian flow in the above range.

  Here, Newtonian flow refers to a phenomenon in which the complex viscosity has a constant value regardless of the frequency, in other words, a rheological behavior in which the frequency and the complex stiffness are proportional.

  As the polysaccharide contained in the digestive enzyme reaction inhibitor / retarding agent of the present invention, any polysaccharide can be used as long as it satisfies the above dynamic viscoelastic parameters. , Xanthan gum, galactomannan (guar gum, locust bean gum, tara gum, etc.), carrageenan, cassia gum, glucomannan, native gellan gum, deacylated gellan gum, tamarind seed gum, pectin, psyllium seed gum, gelatin, tragacanth gum, caraya gum, gum arabic , Gati gum, Rhamzan gum, Psyllium seed gum, Macrohomopsis gum, Agar, Alginic acids (alginic acid, alginate), curdlan, pullulan, methylcellulose (MC), hydroxypropylmethylcellulose (HPMC), carbo Selected from cellulose derivatives such as sodium dimethylcellulose (CMC), hydroxypropylcellulose (HPC), hydroxyethylcellulose (HEC), water-soluble hemicellulose, soybean polysaccharide, processed and modified starch, raw starch (raw starch), dextrin, etc. 1 type or 2 or more types can be mentioned. Preferred are glucomannan and galactomannan, and more preferred is galactomannan.

  Examples of the galactomannan include guar gum and locust bean gum. Guar gum is preferred.

  These polysaccharides are used individually by 1 type or in mixture of 2 or more types.

  These polysaccharides are commercially available or can be obtained by methods known in the art. Furthermore, it is preferable that the average molecular weight of these polysaccharides is adjusted by raw material selection or enzyme / acid treatment.

The average molecular weight of the polysaccharide contained in the digestive enzyme reaction inhibitor / retarder of the present invention is usually 2.0 as the weight average molecular weight when measured by the static light scattering method (concentration and angle dependence of scattering intensity). × 10 ⁶ g / mol or less, preferably 0.05 × 10 ^{6 to} 2.0 × 10 ⁶ g / mol, more preferably 0.5 × 10 ^{6 to} 2.0 × 10 ⁶ g / mol.

  The content of the polysaccharide in the digestive enzyme reaction inhibitor / retarder of the present invention may vary depending on the type of polysaccharide, molecular weight, etc., but is usually 5 wt% or less, preferably 0.01 to 5 wt%. Preferably it is 0.05-3 wt%.

  Examples of the substrate of the digestion reaction that is inhibited by the digestive enzyme reaction inhibition / retarding agent of the present invention include carbohydrates, lipids, proteins, and the like, preferably proteins.

  Examples of the digestive enzyme targeted by the digestive enzyme reaction inhibitor / retarder of the present invention include carbohydrate-degrading enzymes, lipolytic enzymes, and proteolytic enzymes, with the proteolytic enzyme being preferred.

  The digestive enzyme reaction inhibitor / retarder of the present invention includes, as optional components, a fragrance, a colorant, an excipient, a warm feeling, a thermal component, an extract, a surfactant, a solvent, a solubilizer, a pH adjuster, a buffer, Base, anti-packaging agent, emulsifier, suspending agent, softener, thickener, dispersant, excipient, lubricant, antioxidant, preservative, preservative, plasticizer, etc. good.

  By ingesting the digestive enzyme reaction inhibitor / retarder of the present invention together with food, digestion of digestive enzyme substrates such as charcoal fireworks, lipids and proteins contained in the food can be suppressed and / or delayed.

  Examples of foods targeted by the present invention include frozen confectionery such as ice cream, ice milk, lacto ice, sherbet, and ice confectionery; milk, milk beverages, lactic acid bacteria beverages, fruit juice soft drinks, carbonated beverages, fruit juice beverages, vegetable juice beverages , Tea drinks, ion drinks, sports drinks, functional drinks, vitamin supplement drinks, nutritional balance drinks, jelly drinks and powdered drinks; puddings such as custard pudding, milk pudding and fruit juice pudding, jelly, bavaroa Desserts such as yoghurt; Chewing gums, bubble gums and other gums (plate gums, sugar-coated granule gums); chocolates with flavors such as strawberry chocolate, blueberry chocolate and melon chocolate in addition to marble chocolate Chocolates; soft candy Caramels (including caramel, nougat, gummy candy, marshmallow, etc.) and caramels such as toffee; sweets such as soft biscuits and soft cookies; dressings such as emulsification type dressing, separate dressing and non-oil dressing, ketchup, sauce and sauce Sauces; jams such as strawberry jam, blueberry jam, marmalade, apple jam, apricot jam and prasab; fruit wine such as red wine; fruits for processing syrup pickled cherries, apricots, apples, strawberries, etc .; ham, sausage, and Processed livestock products such as grilled pork; fish ham, fish sausage, fish surimi, salmon, bamboo rings, hampen, fried satsuma, date rolls and whale bacon; Bi Noodles such as Hun, Harusame and Wonton; Bread such as bread, confectionery bread and prepared bread, coffee cream, fresh cream, custard cream, whipped cream, creams such as fermented cream and sour cream, consommé soup, potage soup, cream soup And soups such as Chinese soup, soups such as miso soup, fresh soup, stew, curry, and gratin; and various other side dishes and processed foods. In addition to these general foods, protein / phosphorus / potassium-adjusted foods, salt-adjusted foods, oil-and-fat-adjusted foods, intestinal foods, calcium / iron / vitamin-enriched foods, hypoallergenic foods, concentrated liquid foods, and mixer foods , And special foods such as a chopped meal, therapeutic foods, and foods for chewing / swallowing called so-called tromi preparations.

  In this specification, ingesting a digestive enzyme reaction inhibitor / retarder with food (or used with a digestive enzyme substrate) means that the reaction suppressant / retarder is simultaneously with food (or digestive enzyme substrate) at the same time as a meal, Or to be taken after a meal. Here, when the reaction suppressing / retarding agent is ingested at the same time as the food (or digestive enzyme substrate), the reaction suppressing / retarding agent is mixed in the food in advance even if it is separate from the food (or digestive enzyme substrate). It may be.

  In these cases, the ratio of the polysaccharide contained in the digestive enzyme reaction inhibitor / retarder of the present invention is usually 0.5 to 100 mmol, preferably 1 to 100 mmol, more preferably 2 to 1 mol per digestive enzyme substrate. 50 mmol.

  By using the digestive enzyme reaction inhibiting / retarding agent of the present invention so that the number of molar molecules of the polysaccharide contained in the reaction retarding agent is the above ratio, a desired digestive enzyme reaction inhibiting / retarding effect can be obtained. it can. Accordingly, by using a polysaccharide having an average molecular weight adjusted within the above range of addition amount, it is possible to provide a digestive enzyme reaction inhibitor / retarder having a desired effect without greatly changing the physical properties of the system. Can do.

Experimental example 1
Experimental materials and methods Konjac glucomannan (KGM), locust bean gum (LBG), guar gum (GG) as a polysaccharide, isolated soybean protein (SPI) as a protein (molecular weight of about 350,000, the same applies to Example 2), enzyme Pancreatin was used.

  The concentration of the polysaccharide added to the protein was determined in advance so that the zero shear viscosity of the aqueous solution was 10, 20, and 30 mPa · s, and added to the sample (SPI + enzyme + water).

  Table 1 shows the SPI, polysaccharide, and pancreatin concentrations of each sample. Here, the sample name indicates (polysaccharide type-zero shear viscosity of aqueous polysaccharide solution). For example, GG [1] -10 indicates that the concentration is determined so that the zero shear viscosity of the aqueous solution of guagam GG [1] is 10 mPa · s, and the same concentration is added to the sample. Therefore, if the same polysaccharide sample is used, the higher the zero shear viscosity, the higher the polysaccharide concentration, that is, the number of polysaccharide chain molecules present in the system.

Using Leowin (manufactured by Thermo HAAKE), the digestive enzyme degradation process of the polysaccharide-added protein was examined from the time dependence of dynamic viscoelasticity. The time-dependent change of the storage elastic modulus G ′ was approximated by the following equation (Equation 1), and the rate constants k ₁ and k ₂ and the equilibrium value G ′ _3S were obtained using the least square method.

Among the polysaccharide samples used in the experiment, the frequency dependence of the dynamic viscoelasticity of GG [1] aqueous solution (1 wt%) is shown in FIG. 1, and the rate constant (Rate constant) k ₁ of degradation of the polysaccharide-added protein is shown in FIG. As shown in FIG.

The weight average molecular weight of the polysaccharide used was GG [1]: 2.0 × 10 ⁶ g / mol, LBG: 1.0 × 10 ⁶ g / mol, KGM: 1.1 × 10 ⁶ g / mol. Met.

From FIG. 1, the 1 wt% aqueous solution of guar gum used in this experiment always has G ″> G ′, that is, tan δ> 1 (tan δ = G ″ / G) in the frequency range of 0.1 to 100 rad / s. ': Loss tangent). The complex viscosity η ^* = (G ′ ² + G ″ ² ) ^1/2 / ω showed Newtonian equilibrium, and the value was less than 1 Pa · s.

  FIG. 2 shows the rate constant of the protein degradation rate. FIG. 2 shows that the rate constant of the protein added with glucomannan and galactomannan (guar gum, locust bean gum) is smaller than that of the separated soybean protein without added polysaccharide. Therefore, it can be seen that the degradation of the protein is delayed by the addition of the polysaccharide in a relatively low viscosity region (a viscosity region in which the influence of the viscosity on the degradation rate can be almost ignored) of zero shear viscosity of 10 to 30 mPa · s. .

  The comparison of the rate constants for each polysaccharide shows that the galactomannan (guar gum, locust bean gum) mixed system has a smaller rate constant than the glucomannan mixed system, and therefore has a higher protein degradation inhibiting / retarding effect.

  Furthermore, the samples of 30 mPa · s (GG [1] -30, LBG-30, and KGM-30) each having a high zero shear viscosity are 10 mPa · s (GG [1] -10, LBG-10, and Since the degradation rate constant is smaller than that of the KGM-10) sample, it is suggested that the degradation of the protein is delayed when the number of molar molecules of the polysaccharide present in the system is increased.

Experimental example 2
Experimental Materials and Methods Guar gum (GG [1], GG [2], GG [3], GG [4]), isolated soybean protein (SPI) as protein, and pancreatin as enzyme were used as polysaccharides.

  The concentration of guar gum was determined so that the zero shear viscosity of the aqueous solution was 10, 20, and 30 mPa · s, respectively, and added to the sample. Table 2 shows the SPI, guar gum, and pancreatin concentrations of each sample.

Leowin (manufactured by Thermo HAAKE) was used to examine the digestive enzyme degradation process of guar gum-added protein from the time dependence of dynamic viscoelasticity. The time-dependent change of the storage elastic modulus G ′ was approximated by the following equation (Equation 2), and the rate constants k ₁ and k ₂ and the equilibrium value G ′ _3S were determined using the least square method.

Among the guar gum samples used, the frequency dependence of the dynamic viscoelasticity of GG [3] and GG [4] aqueous solutions (1 wt%) is shown in FIGS. 3 and 4, and the rate constant k ₁ of the degradation of the guar gum added protein is shown. As shown in FIG.

The average molecular weight of the guar gum used was GG [1]: 2.0 × 10 ⁶ g / mol, GG [2]: 1.7 × 10 ⁶ g / mol, GG [3]: 1.2 × 10 ^{It was 6} g / mol, GG [4]: 1.0 × 10 ⁶ g / mol.

3 and 4, the 1 wt% aqueous solution of any guar gum always has G ″> G ′ in the frequency range of 0.1 to 100 rad / s, that is, tan δ> 1 (tan δ = G ″). / G ′: loss tangent). The complex viscosity η ^* = (G ′ ² + G ″ ² ) ^1/2 / ω showed Newtonian equilibrium, and the value was less than 1 Pa · s.

  As can be seen from FIG. 5, the rate constant of any guar gum mixed system was smaller than that of the SPI single system, and decreased by about 75%. It was found that the digestive enzyme reaction can be effectively suppressed / delayed by adding guar gum to 2 to 20 mmol per 1 mol of protein which is a substrate for the digestive enzyme.

FIG. 1 shows the frequency dependence of dynamic viscoelasticity of Guar gum GG [1] aqueous solution (1 wt%) in Experimental Example 1. FIG. 2 shows the rate constant k ₁ of the digestive enzyme degradation rate of the polysaccharide-added protein in Experimental Example 1. FIG. 3 shows the frequency dependence of dynamic viscoelasticity of Guar gum GG [3] aqueous solution (1 wt%) in Experimental Example 2. FIG. 4 shows the frequency dependence of dynamic viscoelasticity of Guar gum GG [4] aqueous solution (1 wt%) in Experimental Example 2. Figure 5 shows the rate constant k ₁ of digestive enzymes degradation rate of guar gum added protein in Experimental Example 2.

Claims (6)

Containing polysaccharide, a reaction inhibitor-retarder of digestive enzymes;
The polysaccharide is at least one selected from the group consisting of locust bean gum and guar gum, and the dynamic viscoelasticity of the 1 wt% aqueous solution of the polysaccharide is obtained by using a cone-plate jig having a diameter of 50 mm. When measured at 20 ° C. using a mechanical viscoelasticity measuring device ARES (manufactured by Rheometric Scientific),
(a) G ″> G ′ in the frequency range of 0.1 to 100 rad / s, and
(b) a complex viscosity ^{η * = (G '2 +} G''2) 1/2 / ω indicates a Newtonian equilibrium, wherein the eta ^* is less than 1 Pa · s, the reaction suppression of digestive enzymes -Retarder.
Here, G ′, G ″, and w represent storage elastic modulus, loss elastic modulus, and frequency, respectively. The reaction inhibitor / retarder for digestive enzymes according to claim 1, wherein the average molecular weight of the polysaccharide is 2.0 × 10 ⁶ g / mol or less as a weight average molecular weight when measured by a static light scattering method. Wherein the digestive enzymes a reaction inhibitor-retarder of digestive enzymes to be used with substrates, the proportion of the polysaccharide contained in the reaction inhibiting and retarding agent is a substrate 1mol per 0.5 to 100 mmol of digestive enzymes The reaction inhibitor / retarder for digestive enzymes according to claim 1 or 2. The reaction inhibitor / retarder for digestive enzymes according to any one of claims 1 to 3, wherein the polysaccharide is guar gum. Substrates of digestive enzymes is a protein, the reaction inhibiting and retarding agent of digestive enzymes according to any one of claims 1-4. Digestive enzyme is protease, reaction inhibitor-retarder digestive enzymes according to any one of claims 1 to 5.

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