JPH0736746B2 - Germ drink - Google Patents
Germ drinkInfo
- Publication number
- JPH0736746B2 JPH0736746B2 JP61205523A JP20552386A JPH0736746B2 JP H0736746 B2 JPH0736746 B2 JP H0736746B2 JP 61205523 A JP61205523 A JP 61205523A JP 20552386 A JP20552386 A JP 20552386A JP H0736746 B2 JPH0736746 B2 JP H0736746B2
- Authority
- JP
- Japan
- Prior art keywords
- germ
- extract
- malt
- embryo
- acid solution
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000000284 extract Substances 0.000 claims description 35
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 claims description 21
- 235000013339 cereals Nutrition 0.000 claims description 14
- 238000000605 extraction Methods 0.000 claims description 11
- 239000007788 liquid Substances 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 10
- 150000007524 organic acids Chemical class 0.000 claims description 6
- 239000004615 ingredient Substances 0.000 claims 1
- 210000001161 mammalian embryo Anatomy 0.000 description 16
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 235000013361 beverage Nutrition 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- 241000209140 Triticum Species 0.000 description 5
- 235000021307 Triticum Nutrition 0.000 description 5
- 244000052616 bacterial pathogen Species 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 229920002472 Starch Polymers 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- 235000019698 starch Nutrition 0.000 description 4
- 239000008107 starch Substances 0.000 description 4
- 108091005804 Peptidases Proteins 0.000 description 3
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 3
- 235000015165 citric acid Nutrition 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 235000002906 tartaric acid Nutrition 0.000 description 3
- 239000011975 tartaric acid Substances 0.000 description 3
- 239000008371 vanilla flavor Substances 0.000 description 3
- GHOKWGTUZJEAQD-ZETCQYMHSA-N (D)-(+)-Pantothenic acid Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-ZETCQYMHSA-N 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- GUBGYTABKSRVRQ-DCSYEGIMSA-N Beta-Lactose Chemical compound OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-DCSYEGIMSA-N 0.000 description 2
- GUBGYTABKSRVRQ-PICCSMPSSA-N D-Maltose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- 102000004157 Hydrolases Human genes 0.000 description 2
- 108090000604 Hydrolases Proteins 0.000 description 2
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 2
- 239000004365 Protease Substances 0.000 description 2
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 2
- 108010046377 Whey Proteins Proteins 0.000 description 2
- 102000007544 Whey Proteins Human genes 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 235000020183 skimmed milk Nutrition 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- -1 vitamins B 1 Natural products 0.000 description 2
- 235000021119 whey protein Nutrition 0.000 description 2
- 229930195724 β-lactose Natural products 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- GHOKWGTUZJEAQD-UHFFFAOYSA-N Chick antidermatitis factor Natural products OCC(C)(C)C(O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-UHFFFAOYSA-N 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 102000004139 alpha-Amylases Human genes 0.000 description 1
- 108090000637 alpha-Amylases Proteins 0.000 description 1
- 229940024171 alpha-amylase Drugs 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 229940088598 enzyme Drugs 0.000 description 1
- 235000004626 essential fatty acids Nutrition 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 235000019629 palatability Nutrition 0.000 description 1
- 229940055726 pantothenic acid Drugs 0.000 description 1
- 235000019161 pantothenic acid Nutrition 0.000 description 1
- 239000011713 pantothenic acid Substances 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 241001148471 unidentified anaerobic bacterium Species 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000019156 vitamin B Nutrition 0.000 description 1
- 239000011720 vitamin B Substances 0.000 description 1
- 238000003809 water extraction Methods 0.000 description 1
Landscapes
- Grain Derivatives (AREA)
- Non-Alcoholic Beverages (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は胚芽エキスを含有する胚芽飲料に関し、更に詳
細には穀類の胚芽中に含まれる有用成分をマイルドな処
理で抽出して得た胚芽エキスを含有するおいしい胚芽飲
料に関する。TECHNICAL FIELD The present invention relates to an embryo beverage containing an embryo extract, and more specifically, an embryo obtained by extracting useful components contained in an embryo of a grain by a mild treatment. It relates to a delicious germ drink containing an extract.
穀類胚芽は、良質の蛋白質やヒトの体内では合成されな
いリノール酸、ニコチン酸、パントテン酸等の必須脂肪
酸、ビタミンB1、B2、B6、E、F等の各種ビタミン類、
K、Na、Ca、Mg等のミネラル類を豊富に含有し、栄養価
の極めて高いものである。そして現在、小麦胚芽等の穀
類胚芽の粉末を使用した飲料が食品として市場に提供さ
れているが、これらはいずれも沈降しやすく、引用時の
喉ごしも悪いという欠点があつた。Grain germ is an essential fatty acid such as linoleic acid, nicotinic acid, and pantothenic acid, which are not synthesized in the human body with good quality proteins, various vitamins such as vitamins B 1 , B 2 , B 6 , E and F,
It is rich in minerals such as K, Na, Ca, and Mg, and has an extremely high nutritional value. At present, beverages using powders of cereal germs such as wheat germ are provided on the market as foods, but all of them have the drawback that they tend to settle down and have a bad mouth feel when quoted.
そこで、これらの問題を解決するために、種々の胚芽成
分の抽出方法が提案されている。Therefore, in order to solve these problems, various extraction methods of germ components have been proposed.
例えば、特公昭55−1027号公報には胚芽をデンプン加水
分解酵素の存在下、約70℃で熱水抽出し、更に煮沸処理
して胚芽成分を抽出する方法が、また特開昭48−1170号
公報には三種の酵素を加熱下作用させて胚芽エキスを得
る方法がそれぞれ開示されている。また、特開昭60−14
9351号公報には加水した穀類胚芽に70〜95℃でα−アミ
ラーゼを作用させ、次いで45〜55℃でプロテアーゼを作
用させ、更に加熱処理する胚芽成分の抽出方法が、同60
-149352号公報には膨化処理した全脂穀類胚芽に水の存
在下デンプン加水分解酵素及び/又は蛋白分解酵素を作
用させ、更に加熱処理する胚芽成分の抽出方法がそれぞ
れ開示されている。For example, Japanese Examined Patent Publication No. 55-1027 discloses a method in which the embryo is subjected to hot water extraction at about 70 ° C. in the presence of a starch hydrolase and further subjected to a boiling treatment to extract the germ component. Japanese Patent Laid-Open Publication No. 2003-242242 discloses a method for obtaining an embryo extract by allowing three kinds of enzymes to act under heat. In addition, JP-A-60-14
In 9351, α-amylase is allowed to act on watered grain germ at 70 to 95 ° C., and then protease is allowed to act at 45 to 55 ° C., and a method for extracting a germ component which is further heat-treated, is the same as 60
Japanese Patent Publication No. 149352 discloses a method for extracting an embryo component in which a whole hydrolyzed embryo that has been puffed is treated with starch hydrolase and / or proteolytic enzyme in the presence of water and further heat-treated.
しかしながら、どの方法も収率が悪いか、得られた胚芽
成分に苦があつたり、その嗜好性が低い等味が好ましい
ものでなく、更に改善が望まれていた。However, in any of the methods, the yield is poor, the obtained embryo component is bitter, and the taste with low palatability is not preferable, and further improvement has been desired.
斯る実情において、本発明者らは上記欠点を克服せんと
鋭意研究をおこなつた結果、穀類胚芽の酸溶液抽出物及
びこの抽出物の抽出残査に麦芽を作用させて得た麦芽処
理物液中には、味の良い胚芽成分が多量に含まれている
ことを見出し、本発明を完成した。In such a situation, the present inventors have conducted intensive studies to overcome the above-mentioned drawbacks, and as a result, a malt-treated product obtained by allowing malt to act on an acid solution extract of cereal germ and an extraction residue of this extract. The inventors have found that the liquid contains a large amount of good-tasting germ components, and completed the present invention.
したがつて、本発明は穀類胚芽をpH4〜5.7の有機酸溶
液で抽出して得た抽出物、又は該抽出物とその抽出残
査に麦芽を作用させて得た麦芽処理物液との混合物を主
成分とする胚芽エキスを含有する胚芽飲料を提供するも
のである。Therefore, the present invention is an extract obtained by extracting a cereal germ with an organic acid solution of pH 4 to 5.7, or a mixture of the extract and a malt-treated product liquid obtained by allowing malt to act on the extraction residue. The present invention provides an embryo beverage containing an embryo extract containing as a main component.
本発明において用いられる穀類胚芽としては、麦類、米
類、とうもろこし、その他穀類の胚芽が挙げられ、これ
ら胚芽は全脂物及び脱脂物のいずれでも良い。また、原
料の穀類胚芽の形状は特に制限されるものでなく、例え
ば粉末、粗砕物、圧扁物のいずれをも使用することがで
きる。これら穀類胚芽のうち、特に好ましいものとして
は、脱脂微粉末状の胚芽が挙げられる。Examples of the cereal germ used in the present invention include germs of wheat, rice, corn, and other cereals, and these germs may be whole fat or defatted products. Further, the shape of the grain germ as a raw material is not particularly limited, and for example, any of powder, coarsely crushed product, and pressed product can be used. Among these cereal germs, defatted fine powder-like germs are particularly preferable.
本発明の胚芽飲料を調製するには、まず、穀類胚芽にpH
4〜5.7、好ましくはpH4.5〜5.7の有機酸溶液を加える。
この有機酸溶液量は、胚芽1重量部(以下単に「部」で
示す)に対し3〜6部とするのが好ましい。また、好ま
しい有機酸の例としては、酒石酸、クエン酸、乳酸、リ
ンゴ酸等が挙げられ、特に、酒石酸及びクエン酸が好ま
しい。有機酸溶液による抽出は、機械力若しくは超音波
による攪拌をおこなう場合20〜60分おこなえば良い。つ
ぎに固液分離がおこなわれ、抽出物と抽出残査が分離さ
れる。このときの抽出物の収量は元の胚芽の重量に対し
て乾物換算で約40%前後である。固液分離操作は、常法
によつておこなわれ、得られた抽出物はそのまま胚芽エ
キスとして用いられる。また、分離された抽出残査は麦
芽処理に付される。麦芽処理は、好ましくは抽出残査に
対し、3〜5倍容の水を加え、更に穀類胚芽に対して5
〜25重量%(以下%という)、特に7〜10%の麦芽を添
加し、pHを5.2〜5.8に調整することにより実施される。
この処理温度は、30〜60℃特に40〜50℃が好ましく、ま
た、処理時間は1〜12時間、特に3〜7時間が好まし
い。処理時間が1時間未満である場合は収率が低下し、
また、12時間を超える場合は、菌の増殖により腐敗が生
じる恐れがある。また、酸抽出をおこなわず、元の胚芽
をそのまま麦芽処理した場合にも腐敗が生じる。本発明
で使用される麦芽は、その原料が通常使用されるもの、
例えば六条大麦で良く、その酵素活性は殿粉の糖化力が
10〜40倍、特に20〜30倍のものが好ましい。ここでいう
糖化力は、日本薬局方に準じた方法で測定されるもので
あり、生成麦芽糖量の原料殿粉量に対する倍率で表わさ
れるものである。上記した麦芽処理においては、微量の
プロテアーゼ(例えば10,000I.U.のものを穀類胚芽に対
して0.1%程度)を併用することもできる。このように
して得られた処理物は、80〜120℃で10〜30分間加熱処
理され、更に固液分離に付されて麦芽処理物液が得られ
る。麦芽処理物の収量は、元の胚芽重量に対し、乾物換
算で約30%程度であり、この中には麦芽の自己消化物も
含まれる。なお、固液分離操作も前記と同様常法によつ
ておこなわれる。In order to prepare the germ drink of the present invention, first, the pH of the cereal germ is adjusted to pH.
An organic acid solution of 4-5.7, preferably pH 4.5-5.7 is added.
The amount of the organic acid solution is preferably 3 to 6 parts with respect to 1 part by weight of embryo (hereinafter simply referred to as "part"). Examples of preferable organic acids include tartaric acid, citric acid, lactic acid, malic acid, etc., and tartaric acid and citric acid are particularly preferable. The extraction with the organic acid solution may be carried out for 20 to 60 minutes when stirring with mechanical force or ultrasonic waves. Next, solid-liquid separation is performed, and the extract and the extraction residue are separated. The yield of the extract at this time is about 40% in terms of dry matter with respect to the weight of the original germ. The solid-liquid separation operation is performed by a conventional method, and the obtained extract is used as it is as an embryo extract. The separated extraction residue is subjected to malt treatment. The malt treatment is preferably carried out by adding 3 to 5 volumes of water to the extraction residue, and further adding 5 to the cereal germ.
It is carried out by adding ~ 25% by weight (hereinafter referred to as "%"), particularly 7-10% of malt and adjusting the pH to 5.2-5.8.
The treatment temperature is preferably 30 to 60 ° C., particularly 40 to 50 ° C., and the treatment time is preferably 1 to 12 hours, particularly 3 to 7 hours. If the treatment time is less than 1 hour, the yield will decrease,
Further, if it exceeds 12 hours, spoilage may occur due to bacterial growth. In addition, spoilage occurs even when the original germ is directly treated with malt without acid extraction. Malt used in the present invention, those raw materials are usually used,
For example, six-row barley is good, and its enzymatic activity depends on the saccharifying power of starch.
It is preferably 10 to 40 times, and more preferably 20 to 30 times. The saccharification power here is measured by a method according to the Japanese Pharmacopoeia, and is represented by a ratio of the amount of malt sugar produced to the amount of raw starch. In the above-mentioned malt treatment, a trace amount of protease (for example, about 10,000% of IU can be used in combination with cereal germ). The treated product thus obtained is subjected to a heat treatment at 80 to 120 ° C. for 10 to 30 minutes, and further subjected to solid-liquid separation to obtain a malt-treated product liquid. The yield of the malt-treated product is about 30% in terms of dry matter based on the original weight of the germ, and this includes malt auto-digested products. The solid-liquid separation operation is also carried out by the usual method as described above.
このようにして得られた胚芽成分を含有する抽出物及び
麦芽処理物液は、そのまま、あるいは濃縮して飲料の主
要原料として用いることができる。更に、胚芽成分が変
性しない条件でこれを乾燥して粉末とし、飲料の主要原
料とすることができる。The thus-obtained extract containing the germ component and the malt-treated product liquid can be used as they are or after being concentrated as a main raw material for beverages. Further, it can be dried into powder under the condition that the germ component is not denatured, and can be used as a main ingredient of beverage.
本発明によれば好ましい酸味を有する美味な胚芽成分が
有利に得られるので、経済的であるとともに好ましい胚
芽飲料を提供することができる。According to the present invention, a delicious germ component having a desirable sourness can be advantageously obtained, so that an economical and preferable germ drink can be provided.
次に、実施例及び比較例を挙げて説明する。 Next, examples and comparative examples will be described.
実施例1 (i)脱脂小麦胚芽(水分:12%)(日清製粉(株)
製)をピンミルにて粉砕し、この粉砕物10Kgに、pH4.5
の酸溶液(2%の酒石酸を使用)30lを加えて20分間攪
拌混合し、これを減圧過して抽出液23lと残渣17Kgを
得た。Example 1 (i) Defatted wheat germ (water content: 12%) (Nisshin Seifun Co., Ltd.)
) Is crushed with a pin mill, and 10 kg of this crushed product has a pH of 4.5.
30 l of the acid solution (using 2% tartaric acid) was added and mixed with stirring for 20 minutes, and this was passed under reduced pressure to obtain 23 l of the extract and 17 kg of the residue.
(ii)(i)の残渣に、pH5.5の酸溶液を30l加え、攪拌
混合しながら品温を45℃としてから、麦芽(日本麦芽工
業製)を700g添加して2時間攪拌抽出を行つた。次い
で、温度を90℃まで急速に上げ、同温度に20分間保持し
て殺菌を行なつた。得られた処理物を遠心分離して、抽
出液(麦芽処理物液)26lを得た。(Ii) To the residue of (i), add 30 liters of pH 5.5 acid solution, and while stirring and mixing, bring the product temperature to 45 ° C, then add 700 g of malt (manufactured by Nippon Malt Kogyo Co., Ltd.) and perform stirring extraction for 2 hours. Ivy. Then, the temperature was rapidly raised to 90 ° C. and the temperature was maintained for 20 minutes for sterilization. The obtained treated product was centrifuged to obtain 26 l of an extract (malt-treated product liquid).
(iii)(i)と(ii)で得た抽出液49lをスプレードラ
イヤーにて噴霧乾燥して、粉末胚芽エキス(水分:3.0
%)6.9Kgを得た。この粉末胚芽エキスを用い、以下の
配合のものをミキサーで15分間攪拌混合して胚芽飲料組
成物を得た。(Iii) 49 l of the extract obtained in (i) and (ii) is spray-dried with a spray dryer to obtain powdered germ extract (water content: 3.0
%) 6.9 Kg was obtained. Using this powdered germ extract, the following formulations were mixed by stirring for 15 minutes with a mixer to obtain a germ drink composition.
粉末胚芽エキス :35部 脱脂粉乳 :25 β−ラクトース :20 濃縮ホエー蛋白 :19.5 食塩 : 0.3バニラフレーバー : 0.2 合計 :100 この胚芽飲料組成物10gを150mlの温水に溶解したとこ
ろ、大変美味な胚芽飲料を得た。Powdered germ extract: 35 parts Skim milk powder: 25 β-lactose: 20 Concentrated whey protein: 19.5 Salt: 0.3 Vanilla flavor: 0.2 Total: 100 10 g of this germ drink composition was dissolved in 150 ml of hot water to give a very delicious germ drink. Got
比較例1 実施例1と同様の脱脂小麦胚芽のピンミル粉砕物に、酸
溶液を加えず、はじめから実施例1と同様の麦芽を添加
して2時間攪拌抽出を行なつた。以下、実施例1と同様
の処理を行い、比較品として粉末胚芽エキス(水分3.0
%)6.0Kg(収率66%)を得た。Comparative Example 1 A pin mill pulverized product of defatted wheat germ similar to that of Example 1 was added with malt similar to that of Example 1 from the beginning without adding an acid solution, and extraction with stirring was performed for 2 hours. Thereafter, the same treatment as in Example 1 was performed, and as a comparative product, powdered germ extract (water content 3.0
%) 6.0 Kg (yield 66%) was obtained.
このエキスを用い、実施例1と同様の配合で胚芽飲料組
成物を得、同様に試飲したところ、やや饐えた味で不快
なものであつた。Using this extract, an embryo beverage composition was prepared in the same formulation as in Example 1, and tasting was conducted in the same manner. As a result, the taste was slightly tasteful and unpleasant.
また、実施例1および比較例において、麦芽の処理時間
を、下記第1表に示すように変えた時の麦芽抽出液の一
般生菌数および嫌気性菌数の測定をした。この結果を第
1表に示す。In addition, in Example 1 and Comparative Example, the number of general viable bacteria and the number of anaerobic bacteria of the malt extract were measured when the malt treatment time was changed as shown in Table 1 below. The results are shown in Table 1.
以上の結果から、比較例においては処理時間とともに菌
数が増加し、腐敗が進行していることがわかる。 From the above results, it can be seen that in the comparative example, the number of bacteria increased with the treatment time and the rot progressed.
試験例2 実施例1(i)の抽出液のpHを下記第2表に示すように
変えた以外は実施例1と同様にして粉末胚芽エキスを得
た。この粉末胚芽エキスの収量及び味は第2表の通りで
ある。Test Example 2 A powdery germ extract was obtained in the same manner as in Example 1 except that the pH of the extract of Example 1 (i) was changed as shown in Table 2 below. The yield and taste of this powdery germ extract are shown in Table 2.
実施例2 実施例1(i)及び(ii)で得た両方の抽出液(胚芽エ
キス)を用いて下に示す組成の胚芽飲料を調製した。 Example 2 An embryo beverage having the composition shown below was prepared using both the extract solutions (embryo extracts) obtained in Examples 1 (i) and (ii).
胚芽エキス :80部 牛乳 :19.93 食塩 : 0.04バニラフレーバー 0.03 合計 :100 このものは大変美味であつた。Germ extract: 80 parts Milk: 19.93 Salt: 0.04 Vanilla flavor 0.03 Total: 100 This was very delicious.
実施例3 脱脂小麦胚芽(水分:12%)(日清製粉(株)製)をハ
ンマーミルにて粉砕し、この粉砕物10Kgに、pH5.0の酸
溶液(2%のクエン酸を使用)30lを加えて20分間攪拌
混合した。Example 3 Defatted wheat germ (water content: 12%) (manufactured by Nisshin Seifun Co., Ltd.) was crushed with a hammer mill, and 10 kg of this crushed product had an acid solution of pH 5.0 (using 2% citric acid). 30 l was added and mixed with stirring for 20 minutes.
次に、90℃まで急速に温度を上げ、同温度に20分間保持
して殺菌を行なつた。得られた処理物を遠心分離して、
抽出液24lを得た。この抽出物をスプレードライヤーに
て噴霧乾燥して、粉末胚芽エキス(水分:2.3%)4.1Kg
(収率45%)を得た。Next, the temperature was rapidly raised to 90 ° C., and the temperature was maintained for 20 minutes for sterilization. The obtained treated product is centrifuged,
24 l of extract was obtained. This extract is spray-dried with a spray dryer, and powdered germ extract (water content: 2.3%) 4.1Kg
(Yield 45%) was obtained.
この粉末胚芽エキスを用い、以下の配合のものをミキサ
ーで充分攪拌混合して胚芽飲料組成物を得た。Using this powdered germ extract, the following blends were thoroughly stirred and mixed with a mixer to obtain a germ drink composition.
粉末胚芽エキス 30 部 脱脂粉乳 25 〃 β−ラクトース 24 〃 濃縮ホエー蛋白 20.5〃 食塩 0.3〃バニラフレーバー 0.2〃 合計 100部 このものは大変美味であつた。Powdered germ extract 30 parts Skim milk powder 25 〃 β-lactose 24 〃 Concentrated whey protein 20.5 〃 Salt 0.3 〃 Vanilla flavor 0.2 〃 Total 100 parts This was very delicious.
Claims (1)
して得た抽出物、又は該抽出物とその抽出残査に麦芽
を作用させて得た麦芽処理物液との混合物を主成分とす
る胚芽エキスを含有する胚芽飲料。1. An extract obtained by extracting a cereal germ with an organic acid solution having a pH of 4 to 5.7, or a mixture of the extract and a malt-treated product liquid obtained by allowing malt to act on the extraction residue. An germ drink containing germ extract as an ingredient.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61205523A JPH0736746B2 (en) | 1986-09-01 | 1986-09-01 | Germ drink |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61205523A JPH0736746B2 (en) | 1986-09-01 | 1986-09-01 | Germ drink |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6359863A JPS6359863A (en) | 1988-03-15 |
| JPH0736746B2 true JPH0736746B2 (en) | 1995-04-26 |
Family
ID=16508289
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61205523A Expired - Fee Related JPH0736746B2 (en) | 1986-09-01 | 1986-09-01 | Germ drink |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0736746B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100426960B1 (en) * | 2002-04-12 | 2004-04-13 | 한국식품개발연구원 | A rice beverage containing rice aleuron layer extract, and a method for manufacturing thereof |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5647174A (en) * | 1979-09-27 | 1981-04-28 | Matsushita Electric Ind Co Ltd | Picture quality regulator |
-
1986
- 1986-09-01 JP JP61205523A patent/JPH0736746B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6359863A (en) | 1988-03-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |