WO2004047559A1 - アクリルアミドの生成抑制方法とその用途 - Google Patents
アクリルアミドの生成抑制方法とその用途 Download PDFInfo
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- WO2004047559A1 WO2004047559A1 PCT/JP2003/014819 JP0314819W WO2004047559A1 WO 2004047559 A1 WO2004047559 A1 WO 2004047559A1 JP 0314819 W JP0314819 W JP 0314819W WO 2004047559 A1 WO2004047559 A1 WO 2004047559A1
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- WO
- WIPO (PCT)
- Prior art keywords
- acid
- production
- ability
- acrylamide
- inhibit
- Prior art date
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- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
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Classifications
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- A23L—FOODS, 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
- A23L7/00—Cereal-derived products; Malt products; Preparation or treatment thereof
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- A23L7/109—Types of pasta, e.g. macaroni or noodles
- A23L7/111—Semi-moist pasta, i.e. containing about 20% of moist; Moist packaged or frozen pasta; Pasta fried or pre-fried in a non-aqueous frying medium, e.g. oil; Packaged pasta to be cooked directly in the package
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- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, 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
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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Definitions
- the present invention relates to a method for suppressing the production of acrylamide, which is known as a carcinogenic substance or a substance causing neuropathy, and a thread for use in the method.
- edible materials containing an organic substance having an amino group and a carbohydrate having an ability to form amino or acrylamide can be heated to a relatively low temperature.
- the method for suppressing the generation of acrylamide produced is as follows. When heating edible materials that may produce acrylamide by heat treatment, Acryl characterized in that it contains an organic substance having an ability to inhibit the production of acryl and hydride and is subjected to heat treatment.
- the present inventors have focused on a mechanism for generating an acrylic.
- Organic substances in particular, lactones, substances and / or phenolic substances capable of inhibiting production, and more specifically,
- One or more phenolic substances separated from a conductor are defined as an organic substance having an amino group, and a carbohydrate capable of producing an akulua * on the contrary. The heat treatment in the presence of a specific organic substance does not allow the specific organic substance to be present, and it is believed that the formation of akuUrad 'can be significantly suppressed. Found a new fact, and based on this, made the present invention ⁇
- the present invention provides a method for producing acrylamide-K in an edible material which is likely to produce acrylamide by heat treatment.
- Acrylami characterized by having an organic substance having an inhibitory ability and being subjected to heat treatment.
- To produce acryla by heat treatment comprising an organic substance having an amino group and a saccharide capable of producing acrylamide by reacting with the organic substance.
- the edible material is treated with an organic substance having an ability to inhibit the generation of aku-lu-rad.
- a method for suppressing the production of luer is confirmed, and compositions such as food, drink, cosmetics, pharmaceuticals, or intermediate products thereof, in which the production of acrylamide produced using this method is suppressed.
- Acryladogenesis inhibitor containing an organic substance capable of inhibiting the formation of acrylyl as an active ingredient
- Acrylar F containing an organic substance capable of inhibiting the formation of acrylamide F Foods, cosmetics, pharmaceuticals, PP, Ri good the product of any composition when you provide, the mosquito g
- the edible material which is likely to generate the acryla K by the heat treatment is heated. Reacts with organic substances having an ano group to be added to and / or contained in edible materials and remarkably suppresses the production of acrylamide from substances capable of producing acrylates by reacting with them. You can do it.
- Food production inhibition method ⁇ click re Rua of the present invention or cosmetic PP pharmaceuticals, for the manufacture of or et products soil various compositions between in the) between this to a heart, originating and nervous I 5 early It is possible to produce a highly safe composition which is less likely to cause a notice or the like.
- BEST MODE FOR CARRYING OUT THE INVENTION The edible material that generates acrylamide by the heat treatment according to the present invention includes an organic substance having a 7-amino group and an edible material.
- J Means all edible materials that produce luam o
- organic substance having an amino group examples include, but are not limited to, guanine, L-alanine. Soo-shin, L-Se-un, Heat-train, Shin-chan
- an edible material containing an organic substance having an amino group an organic substance having an N-amino group, or containing one or more of these, for example, agricultural products, Livestock products, marine products or their mouths
- Non-acid and / or nucleic acid seasonings soy sauce, miso, sauce, grilled meat sauce ketchup, V-yonezu, butter, cheese, vinegar, only U Noodles, sake, wine, rye-rail, cinnamon, dash, oysters, oysters, kelp, sushi, shiitake, yeast Seasonings such as ex. And meat ex. 0
- the saccharide having an ability to produce acrylamide according to the present invention there is a saccharide which is supposed to produce akuU ruK in contrast to an organic substance having ano s.
- Non-reducing sugars such as glycerol, as well as glyceric acid, glyceric acid, glyceric acid, and the like.
- O Ascorbic acid is an example of a non-ascorbic acid conductor.
- an edible material having a quality capable of producing a lacquer, a carbohydrate, or a carbohydrate having one or more of the above saccharides for example, cinnamon products, livestock, Water organisms or their PP can be mentioned more specifically.
- cinnamon products, livestock, Water organisms or their PP can be mentioned more specifically.
- the following quality is required.
- m Candy Sugar sweeteners such as lactose and sugar can be mentioned.
- the edible material containing an organic substance having an a group, an organic substance having a no group, and / or a saccharide and a saccharide capable of forming a product by reacting with the above is specifically described in the example of food and drink.
- seasonings and sweeteners for example, sliced potatoes, boiled, steamed fish, potatoes, potatoes to be reconstituted, potato flour germinated wheat Wheat flour, wheat germ, dough, gluten germinated barley, germinated rice, rice grits, rice flour, corn, corn flour, buckwheat flour, soy flour, defatted soybean, Soybean power Zein Boiled beans, pasted beans, germinated soybeans, etc., and can be produced by mixing one or more of these materials.
- premix products such as sponge, nuts, donut mix, tempura powder, tempura seeds, salad mix, etc. and intermediate PP Products and their processed products, including, for example, brewery or A-frozen meat, carcass, milk, skim milk, and raw cream — Luke power zein, knotter, tea Livestock products such as meat, whey, whole eggs, liquid eggs, egg yolks, egg whites, boiled eggs, or their processing
- O PP Furthermore, for example, marine products such as chilled or frozen fish, fillets, surimi, dried fish s baked shellfish, or processed products thereof o
- organic substance having an ability to inhibit the production of acrylamide refers to an edible material containing the organic substance having the ano group and the saccharide having the ability to produce acrylamide.
- the term refers to all organic substances that have the effect of suppressing the production of acrylamide by allowing them to survive heat treatment.
- Acrylic is an example of an organic substance having the ability to suppress K production.
- the quality having the ability to inhibit the production of akuUrad 'is for example,-trehalose, 1 ⁇ -l-trehalose reduction, j-latinose-g Lecosil a-
- phenolic substances that have the ability to inhibit the production of alkamine are: catechin, epir dyke Flavonoids such as kins and other power technics, kercetin, isoscelsitol U, lutin, na U, hesdin, etc.
- Phenolic substances such as conductors
- One or more selected from the organic substances can be advantageously used in the present invention.
- ⁇ -treno ⁇ ⁇ ⁇ and / or ⁇ -treno ⁇ ⁇ -Carbohydrates such as sugars, and other fluorogenic substances such as rutin, nanzine and / or heparin are organic compounds containing ano groups and acrylates.
- a is a high-purity lipstick a, ⁇ -trehalose (registered trademark “Treha” sold by Hayashibara Shoji Co., Ltd.) , ', The reagent grade crystals are ⁇ , 5-toreha ⁇ ls (sold by Hayashibara Biochemical Research Laboratories, Inc. ) May be powdered reduced para- noses (Mitsui Sugar Sales, product name “Paratinite”) or
- Trilin can be advantageously used, for example, high-purity ⁇ -cyclodextrin (sold by Shiosui Port Refining Co., Ltd., trade name: “Digi-Pearl 3-1 ⁇ 0”).
- the phenolic substance having an ability to inhibit the production of acrylylamide in the present invention is, for example, commercially available.
- Phenolic substances, such as propyl and plant cyanidins or their carbohydrate derivatives, are originally sold as health foods
- green tea polyphenol (Tokyo Food) may be used as a catechin.
- Techno Co., Ltd., registered trademark “Polyf; 1: Non”) Doga or flavonoids include sugar karuta (Rinbara Shoji Sales Co., Ltd.
- An organic substance or a substance having an ano group is an organic substance or a substance having an ano group
- the molar ratio is 0.5 or more, ⁇ 0.7.5 or more, more preferably 1.0 or more, with respect to cryla or a carbohydrate capable of producing. It is desirable. If the molar ratio is less than 0.05, the presence of lacquer is not sufficient, and the organic substance having the ability to inhibit acrylamide formation may not be effective. In the case of phenolic substances, the molar ratio is preferably 0 • 004 or more, with respect to the organic substance having an a / no group or the carbohydrate capable of forming an alkanol. Then ⁇ is 0.
- an organic substance having an amino group contained in an edible material reacts with a substance having an ability to produce acrylamide to form an acrylate.
- the method of heating is particularly limited For example, for example, for example, baked ⁇ s Roasting, heating a child range s lettuce heating
- the organic substance having the acrylamide production suppression base in the present invention is different from the sample (edible material) in terms of the moisture content of the sample (edible material). It is possible to suppress the generation of acrylic at any of the low-cost sites. In particular, in order to remarkably suppress the production of acrylic acid, the water (a) of the sample (edible material) during the heat treatment is usually preferably about 10% by mass or more. The use of the method for suppressing the generation of acryl is suppressed by the
- the operation of adding the edible material to the edible material may be performed before the edible material is subjected to the heat treatment, even at the stage of blending the raw material for preparing the edible material. Addition immediately after heat treatment and / or / 't A
- Examples of the method of inclusion include, but are not limited to, kneading, kneading, dissolving, dispersing, suspending, emulsifying,
- the method of application, spraying, injection, etc. can be selected as appropriate.o Generating acryla in plant cells such as fruits, etc. through gene manipulation as necessary It is advantageous to pre-generate an organic substance having a suppressing ability, for example, a quality and / or phenolic substance, and to have it in the mouth to make it an edible material.
- the organic matter m. Having the ability to inhibit the production of aqua described in the item IJ is included in the edible material that produces the acrylamide by heat treatment. Finished with edible materials and oral compositions with the ability to inhibit the production of acryla
- the organic substance having the above-mentioned ano group and / or the substance having the ability to inhibit the production of acrylamide and / or the phenol compound having the ability to inhibit the production of acrylamide can be used.
- a carbohydrate having the ability to produce acryla described in HIJ it can be advantageously carried out to obtain a composition having the ability to inhibit the production of urea.
- Gu-Sin-Sin-Sin-Sin-Sin-Sin-Sin-Sen-Sin N Gu-Sin-Sin-Sin-Sin-Sin-Sin-Sen-Sin N
- Organic substances such as peptides or proteins having an S-no group, and D-x-ss-arabinos: D, G-co-,
- One or more monosaccharides selected from D-fructose and D-galactose D-xix, s--arabino--s,
- D-Glucos D-Fractus and D-galactose-one or two or more T-shells are used as constituent sugars.
- Non-complex sugars are used as constituent sugars.
- -Is more than 0.5, preferably 0.75 or more, in mole ratio. More preferably, ⁇ is 1 • 0 or more, and as a phenolic substance having an ability to inhibit Z or acrylamide formation, for example, rutin, naringin and / or Or hesperidin in a molar ratio of 0.
- the composition has the ability to suppress the formation of U-Ru amide, and even if this is heated alone or with other materials, the formation of acrylamide is remarkable. It is possible to obtain an excellent effect that it is suppressed and its formation is substantially prevented.
- an organic substance having the ability to inhibit the production of acrylamide as described in BIJ is to be mixed with and contained in ascorbic acids.
- the solid composition of the present invention can also be advantageously implemented.
- Such a composition containing oral cholesteric acid is a composition that requires acetic acid, and is additionally prepared by heat treatment. By using it in the manufacture of compositions containing edible materials that may produce acrylamide, it is possible to effectively produce acrylamide in those processes. Can be suppressed.
- Such a composition containing lascosulbic acids is a highly safe, high PP drinking porcelain that is enriched with lascosolebinic acids (vinyl, N-C).
- the food or drink of the composition described above may be a food or drink manufactured in an orderly manner for animals including humans and pets, for example, a pot-tip chip. , Floats, Floyd Onions, Conch Chips, Bananas, Vegetable Chips, Fried Senbei, University of Umpei, Kanto, Sunna Fried confectionery such as confectionery cakes ⁇ okke, potato, fries, tempura, fried food, fried Satsuma ginger balls, thick fried spring rolls, instant fried foods, etc., senbei Japanese sweets such as hail, dorayaki, middle, bun, sea bream takoyaki, barley, biscuit, krak power, cooki-pretelle, seria Confectionery, snacks, lollipops, nons, pizzas, pies, sponges - key, full Tsu full, force the scan Te La, de over Na Tsu of how small MugiKae ⁇
- cosmetics include, for example, lotions, creams, emulsions and gels. Soap, toilet soap, skin wash powder, face wash cream, etc. in the form of, powder, paste, block, etc., ⁇ , ⁇ , J J J J J ⁇ ⁇ ⁇ ⁇ For example: jump-bottle-line, jumper, lens, hair-washing powder, etc .: raw
- Cosmetic cosmetics such as jelly-like pill-shaped type, jelly-like fillet type, paste-type wash-off type, powdery, etc.
- Cream cold cream, hand cream, hand cream, emulsion, moisturizer, shower ⁇ One-third, Shearing ⁇ -One, Three-Phase ⁇ BING FORM, PRESH-BREAK Cosmetic oil, Baby
- Oral cosmetics such as nail cosmetics, cosmetics, lipsticks, lip creams, condensed lipsticks, lip glosses, lip cosmetics, toothpastes, and mouthwashes
- the cosmetic PP obtained by using the method for inhibiting the production of acrylics according to the present invention is exemplified by durable cosmetics, nossolt, bath cosmetics such as bath cosmetics. Even after the heat treatment, the amount of lactam is remarkably reduced, causing less onset and neurological damage.
- composition which can be produced by employing the method for suppressing the production of acrylic acid according to the present invention, such as 1 1
- Agents Excipients Excipients Capsules, tablets, pills, ophthalmic softeners Oral mucosal patches Suspensions, emulsions, hardeners, drugs, suppositories, powdered liquors, tablets, tablets Injection, tincture, ophthalmic occupational occupation " ⁇ Ear occupational occupational agent Agent
- the obtained pharmaceuticals are heat-treated to reduce the risk of carcinogenesis and nervous disorders by significantly reducing the risk of carcinoma and nervous disorders.
- the K-generation 5 formula test was performed using a phenolic acid according to the method of Nulless Mottleram (D0 ⁇ aIdS • ⁇ 0ttram) described in Non-Patent Document 2.
- Carrier gas helium (1 mI / min)
- the test results are shown in Table 1.
- the acrylamide production rate (%) is based on the assumption that the amount of acrylamide produced when using D-glucose as the carbohydrate is 100%.
- the values are shown as relative values.
- D-glucose, D-fructoose, and succorbic acid in the heat treatment with sanolagine are comparative. It produced a pajamas of the evening. Above all, the production of acrylami from ascorbic acid was more than four times as large as that of D-glucose mouth, and D-glucose was large. And D-fractures are few in comparison to ca, but D-galactoses and malt souks.
- the heat treatment with spargin has produced the U-family F o- ⁇ ⁇ ⁇ The heat treatment has been carried out and the heat treatment has been carried out. No production of aqua and de from the yeast was observed. ⁇ It is an asymmetric carbohydrate.
- the production rate of L-Lu and L-glucose from D-glucose is reduced to 50% or less.
- Uru 7 *, « «. 'The production rate (%) was significantly less than 20%.
- the mole ratio in the table is the mole ratio of a-trace to D-glucose, and the s-quard 'production rate (%) is D-glu
- Tre a, a-Trehalose
- D-glucose is increased by increasing the amount of D-glucose, but the amount of lacquer is increased.
- the mole ratio of a-to-reno-square to a mixture is 0.5 or more within the range of the ⁇ -test, the 7- ) Is the additive system
- the amount of acrylamide generated (kmg) is set to a relative value of 100%.
- the amount of akulua produced by heating with D-glucose varies depending on the type of anoic acid.
- the results of Table 5 that the anoic acids that produce quorum F are asparagine and L-isosicin, the results are shown in Table 5. Reno ⁇ ⁇ --source was found to significantly suppress the generation of aquarium from shiso-shisin as well as shi-paragin.
- the generation to the aku-u-lua is performed by the program of the para-paragine and the L-isocyanin.
- a sugar solution (saccharide content: 0.1 mM 01 / mI) was added to a 0 ml volume test tube with a stopper in 1 ml and 0.05 M phosphate buffer (p.
- the water content of the sample is about 5
- the results are shown in Table 7.
- the acrylamide production rate (%) was shown as a relative value when the amount of acrylamide production (mg) at each water content of the control sample was 100%.
- V 8 Content (3 ⁇ 4) Acrylamide Acrylamide m Production ung) Production rate) Production quantity (mg) Production rate
- the processing was performed in the same manner as in Experiment 6 except that the values were changed to 0 • 100 and 0500 mmoI, and the production amount of acrylamide was measured.
- Table 8 shows the results obtained when the same treatment was carried out in the test system without the addition of urea.
- the acrylamide production rate (%) was shown as a relative value when the amount of acrylamide (mg) in P-I was 100%. .
- BIR of edible materials such as fruits or wild rice.
- the three types of kiston are-0 200 m 9 (about 0 • 1 7
- the acrylamide formation rate (%) is calculated by subtracting the amount of acrylamide formation (mg) when only L-asparagine and L-ascorbic acid are used. It is shown as a relative value when it was taken as 0%. Table 9
- Cyclic tetrasaccharide A cyclic tetrasaccharide in which four molecules of D-glucose are alternately linked by a 1,6 or ⁇ -1,3 bond.
- ⁇ S-D ⁇ Entrance D ⁇ Eli-Sitol, Reducing Platinum ⁇ Glucose J ⁇ , ⁇ Tre / ⁇ Loose, Nanamaru Cyl-trehalose and c-cyclodextrin are asparagine, L-ascorrebinic acid and power, and their acrylates and dough. Production rate to less than 50%, in particular, ⁇ ,
- T re Hi, ⁇ -Treha mouth
- the fluctuation of PH before and after the heat treatment was small in both the system with and without the addition of heat, and the sample used was small. It is low, so the production is small, but it has been found that fac-U-lua is produced at the mouth of heated f100 ° c.
- -Trehalose The production of aqua in the non-added system increased as the reaction pH increased, and increased drastically in PH 6 and PH 6-5. Even at pH, the formation of akulua was significantly lower than that of the added system.
- the degree of suppression is almost constant, and under the conditions in which the production rate (%) of aqua is suppressed to less than 15%, casparagin or L
- S-Sulfuric acid instead of S-sulfuric acid 5 S-Sulfuric acid 2-sulfuric acid (Hashiwara Biochemical Research Kyushu Sales Co., Ltd.) Indication AA 2 GJ) or scorubic acid 2-U acid ( ⁇ Shu Vita, 3N
- the generation rate (%) of 7 cl 7 mid in the table shown in Fig. 4 is Under the respective pH conditions, when the amount of acrylylamide formed (mg) in the absence of ⁇ , ⁇ -trihalose was 100%, The relative values of the rose addition system are shown.
- 2-Gluco-K is more stable to heat treatment than sea-scorbic acid and has a heat treatment degree of 100 ° C.
- the amount of acrylamide generated is lower than that of ascorbic acid, but under the condition of pH less than PH4, it is less than that of ascorbic acid. Generates more than 10 and Tari aquaria, and in the case of trees exceeding s PH6-same as ashcorubic acid
- rutin, naU and hesin are present in a relatively small amount of ⁇ t, i.e., in a molar ratio relative to cis-g or G-glucose. 0. 0 0
- a-Torreha ⁇ Issuri is a dry mash 3.
- a-Torreha ⁇ Issuri is a dry mash 3.
- the dried potatoes used in the experiment had a water content of 7.2% by mass.
- the solid phase extraction column (commercial name: Oasis HBL5) was preliminarily confined with methanol 5I and 5 ml of deionized water. 0 mg power cartridge, manufactured by Nihon Waters Co., Ltd.) and eluted 10 times with 2 ml of deionized water, for a total of 10 fl. Fractionated into cushions. Flux 3 containing 'U-U-Lad' was filtered and used as a material for analysis of A-Frilla F. o In this experiment,
- the C-MS analysis was carried out using a C / MS / ⁇ S system (Thermoc: c-Stor Co., Ltd.) Went on condition o
- Measurement time 10 minutes (c Introduce 4 to 7 minutes of analysis time to the source)
- Table 13 shows the o ⁇ expression results obtained by multiplying the measured values obtained by multiplying the degree of the internal standard by the above three times and multiplying them by the above-mentioned effect. Faku Uru, Uto 'is generated by the Flippo
- the actual food is cooked using PP material
- This PP contains ⁇ ,,-ureno ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ PP PP ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP PP
- Jagamo (northern M extra-production, make-in) is washed with whole water and then put into a shredder to make a square pillar-shaped shredded piece of about 1 cm on a side. 1% and 20% by weight of,
- ⁇ Treha ⁇ ⁇ S (Hayashibara Shoji Co., Ltd., registered trademark “Treno”) Aqueous solution: and immersed in it and kept at 50 ° C for 20 minutes. Draining was performed, followed by blanching for 3 minutes.Frozen / Pb-preserved at _20 ° C, and then fried in accordance with a conventional method to prepare a fly pot.
- This BP is good in shape, texture and flavor, and contains., ⁇ -ray 1 ⁇ ⁇ , so it can be purified by fly processing. It is a highly safe flooded potato with reduced generation of mist, and can be used as it is, or as an advantage, as a soup.
- Example 3
- 70 parts by mass of flour, 0.25 parts by mass of yeast and 30 parts by mass of water are kneaded to prepare a medium seed, and then a low strength is applied to the medium seed.
- This product has a good flavor and good taste.- Because it does not eat trehalose, it is safe to prevent the production of acrylamide by firing. This product, which is a highly resistant cracker, can be used advantageously as a snack.
- M Western yeast manufactured by Sanfuji Corporation 2 parts by mass, 12 parts by mass of whole egg, 10 parts by mass of unsalted butter-20 parts by mass of milk, 75 parts by mass of water After kneading at 24 ° C at low speed for 6 minutes and medium speed for 5 minutes and then stopping, kneading was further continued at medium speed for 4.5 minutes to produce a raw material. Fermentation was performed for 50 minutes as one time. The dough is divided into 40 g pieces, rounded and
- This product is generally swollen, has a good color tone, has a good taste, and contains a, -trinoperose. It is a highly safe butter roll in which the generation of cryamide is suppressed.
- slice arms were treated at 70 ° C with a concentration of about 5 Ow / w% ⁇ , ⁇ -trehalose (Hayashibara Biochemical Co., Ltd.) Immersion in a solution for 15 minutes, draining, and then using an electronic oven.
- This PP can be used as a snack or as a confectionery or confectionery ingredient.
- the dried rice is further roasted in a conventional manner, and the roasted germ is prepared.
- the oat is good in flavor and contains a mixture of nutrients. Therefore, it is a highly safe pre-roasted wheat germ with reduced production of acrylado by roasting.o
- This product is savory ⁇ easy to eat and storage stable O
- this product is a mineral vitamin containing selenium zinc and a food fiber.
- Example 7 Since the rice is contained in rice fields, it is suitable as a raw food for stomach feeding pm 1 or as a raw material for other drinks o
- Example 7 Since the rice is contained in rice fields, it is suitable as a raw food for stomach feeding pm 1 or as a raw material for other drinks o
- Example 7 Since the rice is contained in rice fields, it is suitable as a raw food for stomach feeding pm 1 or as a raw material for other drinks o
- dry mass potato (trade name “Queen's Shef Mass Potato” manufactured by Miki Foods Co., Ltd.) 100 parts by mass and high-purity hydrous crystals ⁇ , ⁇ -toluene Lehalose powder (Hayashibara Shoji Co., Ltd., registered trademark “Toreha”) 2.5 parts by weight were uniformly mixed to produce powder 7-ZL powder.
- This product contains a., O ⁇ -tore / ⁇ ⁇ -- ⁇ ⁇ : :: ⁇ O> ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ It is a highly safe powder that can be used with wild rice and other ingredients to suppress the formation of akulua when oiled.
- Example 8 Powder and powder obtained in Example 8 3. 100 Potatoes Dish and pepper are added to the shellfish and milk is added.
- the mixture was kneaded to obtain a dough.
- This material was rolled to a thickness of 2 mm, and then cut to a width of 5 mm to obtain a pretzel material.
- the dough was heated at 230 to 260 ° C for 6 minutes to prepare a crisp pretzel. Since this product contains, ⁇ -torenolose, it is a highly safe crystal that suppresses the production of acrylamide when fired. It is a pre-order o
- this product contains ⁇ , ⁇ -trehalose together with L-ascorbic acid, it is a composition that requires L-ascorbic acid. And heat-treating this together with an edible material that may react with lacsorbic acid to form acrylamide to produce another composition Even in this case, it is possible to effectively suppress the generation of acrylamide in the manufacturing process.
- This product is a granule with good fluidity with no caking, easy handling and good storage stability, and safety containing L-ascorbic acid. It can be advantageously used for producing various compositions such as foods and drinks, cosmetics, pharmaceuticals or intermediate products thereof with high quality.
- L-ascorbic acid 2 Glucoside powder (available from Hayashibara Biochemical Laboratory Co., Ltd., registered trademark “AA2G”) 1 part by mass and high-purity hydrous crystals ⁇ , ⁇ —Treha And 9 parts by mass of a low-grade powder (Hayashibara Shoji Co., Ltd., registered trademark “Treha”) were mixed uniformly to obtain a powdery laccolnic acid-containing composition.
- this product contains ⁇ , a-torenolose together with L-ascorbic acid 2 —glucose, it can be treated with L-ascorbic acid. , Which may react with L-ascorbic acids to form acrylamide. Heat-treating the material together with the other ingredients to produce another composition.
- This powder is a powder that has been prevented from caking, has good mobility, and is easy to handle and has good storage stability. Highly safe PP mouth with acids
- compositions such as quality foods and drinks, cosmetic and pharmaceutical taps or intermediates between them.
- This composition has a ratio of 1-to-1 and mono-to-transferred rutin with bis-sulfuric acid. And do this,
- the edible ingredients and other ingredients are heat-processed to produce another composition.
- L-Iscorubic acid 2 Glucose Y (Hayashibara Biochemical Research Laboratories Co., Ltd., registered trademark “AA2G”) 10 parts by mass Propylene glycol 50 Parts by mass Purified water 30 • 5 parts by mass
- This product is used in combination with anoic acid and L-aspartic acid 2-glycoside in combination with ⁇ , -trihalose and ⁇ -triure. Because it contains noose, it is an emollient cream that suppresses the production of acrylic acid by heat treatment.This product also has excellent moisture retention. In addition, it has good growth and gloss ⁇ and is suitable as a highly safe cosmetic.
- Example 17
- amino acid mixture 4 parts by mass of isolysin, L — 6 parts by mass of rosin, L — 8 parts by mass of lysine hydrochloride, L-phenylalanine 8 parts by weight, L — 1 part by weight of tyrosine, L — 8 parts by weight of ripple phantom, L — 8 parts by weight of parin, L — 1 part by weight of phosphoric acid, A mixture of 1 part by mass of L-serine, 1 part by mass of L-methylamine, 2 parts by mass of L-trionin, and 8 parts by mass of L-arginine hydrochloride was prepared.
- thiamine nitrate 0.01 parts by weight 1-cotin acid amide 0 • 0.44 shellfish part, water 86.05 parts by weight
- this PP refers to ⁇ -noic acid and L-ascorbic acid 21-glucose, as well as -trehalose and ⁇ -1 It is preferable as a highly safe amino acid-containing linking agent in which the generation of acrylamide by heat treatment is suppressed.o Industrial applicability How to control the production of acrylamide
- compositions that have the ability to inhibit the production of luamide can be used in agricultural products, livestock, marine products or their processing.
- the sugar having the ability to produce acrylamide is L-l-rubic acid
- a sulfonic acid-containing composition having the ability to inhibit the production of 'acrylamide' is a composition that requires ash corbins, which, in addition, produces an alkanol by heat treatment.
- the invention is a food and drink cosmetic PP pharmaceutical PP or ih
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Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
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DE60329015T DE60329015D1 (de) | 2002-11-27 | 2003-11-20 | Verfahren zur hemmung der acrylamidbildungund seine verwendung |
EP03811909A EP1568283B1 (en) | 2002-11-27 | 2003-11-20 | Method of inhibiting acrylamide formation and use thereof |
CN2003801044596A CN1717181B (zh) | 2002-11-27 | 2003-11-20 | 丙烯酰胺的生成抑制方法及其用途 |
US10/536,268 US20060194743A1 (en) | 2002-11-27 | 2003-11-20 | Method for inhibiting acrylamide formation and use thereof |
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JP2002-344613 | 2002-11-27 | ||
JP2002344613 | 2002-11-27 | ||
JP2002-372115 | 2002-12-24 | ||
JP2002372115 | 2002-12-24 | ||
JP2002378582 | 2002-12-26 | ||
JP2002-378582 | 2002-12-26 | ||
JP2003027433 | 2003-02-04 | ||
JP2003-27433 | 2003-02-04 | ||
JP2003057582 | 2003-03-04 | ||
JP2003-57582 | 2003-03-04 | ||
JP2003-86324 | 2003-03-26 | ||
JP2003086324 | 2003-03-26 | ||
JP2003-282087 | 2003-07-29 | ||
JP2003282087A JP2004305201A (ja) | 2002-11-27 | 2003-07-29 | アクリルアミドの生成抑制方法とその用途 |
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WO2004047559A1 true WO2004047559A1 (ja) | 2004-06-10 |
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US (1) | US20060194743A1 (ja) |
EP (1) | EP1568283B1 (ja) |
JP (1) | JP2004305201A (ja) |
KR (1) | KR20050074643A (ja) |
CN (1) | CN1717181B (ja) |
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Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004098313A1 (de) * | 2003-05-08 | 2004-11-18 | Helmut Ritter | Verminderung von acrylamid in lebensmitteln |
CN1313036C (zh) * | 2005-03-21 | 2007-05-02 | 浙江大学 | 竹叶提取物作为热加工食品中丙烯酰胺抑制剂的应用 |
WO2007097357A1 (ja) * | 2006-02-22 | 2007-08-30 | Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo | 揮発性硫化物類の生成抑制剤とこれを利用する揮発性硫化物類の生成抑制方法 |
US7267834B2 (en) | 2003-02-21 | 2007-09-11 | Frito-Lay North America, Inc. | Method for reducing acrylamide formation in thermally processed foods |
KR100830680B1 (ko) * | 2005-11-03 | 2008-05-20 | 주식회사농심 | 아크릴아마이드가 저감된 스낵의 제조 방법 |
US7393550B2 (en) | 2003-02-21 | 2008-07-01 | Frito-Lay North America, Inv. | Method for reducing acrylamide formation in thermally processed foods |
US7811618B2 (en) | 2002-09-19 | 2010-10-12 | Frito-Lay North America, Inc. | Method for reducing asparagine in food products |
US8110240B2 (en) | 2003-02-21 | 2012-02-07 | Frito-Lay North America, Inc. | Method for reducing acrylamide formation in thermally processed foods |
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Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7811618B2 (en) | 2002-09-19 | 2010-10-12 | Frito-Lay North America, Inc. | Method for reducing asparagine in food products |
US8110240B2 (en) | 2003-02-21 | 2012-02-07 | Frito-Lay North America, Inc. | Method for reducing acrylamide formation in thermally processed foods |
US8114463B2 (en) | 2003-02-21 | 2012-02-14 | Frito-Lay North America, Inc. | Method for reducing acrylamide formation in thermally processed foods |
US7267834B2 (en) | 2003-02-21 | 2007-09-11 | Frito-Lay North America, Inc. | Method for reducing acrylamide formation in thermally processed foods |
US7393550B2 (en) | 2003-02-21 | 2008-07-01 | Frito-Lay North America, Inv. | Method for reducing acrylamide formation in thermally processed foods |
WO2004098313A1 (de) * | 2003-05-08 | 2004-11-18 | Helmut Ritter | Verminderung von acrylamid in lebensmitteln |
CN1313036C (zh) * | 2005-03-21 | 2007-05-02 | 浙江大学 | 竹叶提取物作为热加工食品中丙烯酰胺抑制剂的应用 |
KR100830680B1 (ko) * | 2005-11-03 | 2008-05-20 | 주식회사농심 | 아크릴아마이드가 저감된 스낵의 제조 방법 |
WO2007097357A1 (ja) * | 2006-02-22 | 2007-08-30 | Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo | 揮発性硫化物類の生成抑制剤とこれを利用する揮発性硫化物類の生成抑制方法 |
US8343951B2 (en) | 2006-02-22 | 2013-01-01 | Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo | Volatile sulfide production inhibitor and method for inhibiting the production of volatile sulfide using the inhibitor |
US8486684B2 (en) | 2007-08-13 | 2013-07-16 | Frito-Lay North America, Inc. | Method for increasing asparaginase activity in a solution |
US8158175B2 (en) | 2008-08-28 | 2012-04-17 | Frito-Lay North America, Inc. | Method for real time measurement of acrylamide in a food product |
US9095145B2 (en) | 2008-09-05 | 2015-08-04 | Frito-Lay North America, Inc. | Method and system for the direct injection of asparaginase into a food process |
US9215886B2 (en) | 2008-12-05 | 2015-12-22 | Frito-Lay North America, Inc. | Method for making a low-acrylamide content snack with desired organoleptical properties |
US8284248B2 (en) | 2009-08-25 | 2012-10-09 | Frito-Lay North America, Inc. | Method for real time detection of defects in a food product |
WO2018169055A1 (ja) | 2017-03-16 | 2018-09-20 | 学校法人北里研究所 | 新規ポコニオライド化合物及びその使用 |
Also Published As
Publication number | Publication date |
---|---|
DE60329015D1 (de) | 2009-10-08 |
CN1717181B (zh) | 2010-05-05 |
EP1568283A1 (en) | 2005-08-31 |
KR20050074643A (ko) | 2005-07-18 |
CN1717181A (zh) | 2006-01-04 |
US20060194743A1 (en) | 2006-08-31 |
EP1568283A4 (en) | 2007-02-28 |
EP1568283B1 (en) | 2009-08-26 |
TW200501886A (en) | 2005-01-16 |
JP2004305201A (ja) | 2004-11-04 |
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