JPH08168388A - Production of aloe extract flavor - Google Patents
Production of aloe extract flavorInfo
- Publication number
- JPH08168388A JPH08168388A JP6334484A JP33448494A JPH08168388A JP H08168388 A JPH08168388 A JP H08168388A JP 6334484 A JP6334484 A JP 6334484A JP 33448494 A JP33448494 A JP 33448494A JP H08168388 A JPH08168388 A JP H08168388A
- Authority
- JP
- Japan
- Prior art keywords
- yeast
- aloe extract
- lactic acid
- water
- added
- 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.)
- Pending
Links
Landscapes
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Medicinal Preparation (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、民間薬として利用され
るアロエの抽出物の苦味と青臭みを矯正し、飲用し易く
するアロエ抽出物矯味剤の製造方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing an aloe extract corrigent that corrects the bitterness and blue odor of an aloe extract used as a folk medicine and makes it easier to drink.
【0002】[0002]
【従来の技術】ユリ科アロエ属の植物は、古い時代から
民間薬草として利用されているものである。その種類は
多いが、わが国の気候風土に適するものとしてキダチア
ロエが普及している。民間薬としての利用形態は、多肉
性の葉をすりおろしたり、生のまま輪切りにして水で煮
出した液を飲用し、胃弱、便秘、せき、ぜんそくなどに
使っている。アロエの主成分は結晶性のアロイン(al
oin)、アロエエモジン(aloe−emodin)
などであって、いずれも強い苦味を示す(木島正夫等編
『薬用植物大事典』修正版第23〜24頁、広川書店、
1967:木村康一・木村孟淳共著『原色日本薬用植物
図鑑』改訂版第234頁、保育社、1981)。2. Description of the Related Art Plants belonging to the genus Aloe of the family Liliaceae have been used as folk herbs since ancient times. There are many kinds, but Kidachi aloe is popular as one suitable for the climate of Japan. It is used as a folk medicine by succulent leaves grated or sliced raw and boiled in water for drinking, and is used for stomach weakness, constipation, coughing, asthma, etc. The main component of aloe is crystalline aloin (al
oin), aloe-emodin
And so on, all of which show strong bitterness (edited by Masao Kijima et al., “Encyclopedia of Medicinal Plants”, revised pages 23 to 24, Hirokawa Shoten,
1967: Koichi Kimura and Jun Kimura, "Primary Color Japanese Medicinal Botanical Encyclopedia," revised edition, page 234, Nursery School, 1981).
【0003】キダチアロエの抽出液は苦味が強く、ま
た、青臭みを持つため、民間薬ないし保健飲料として利
用しにくいのが欠点である。そこで、アロエから特殊な
蒸留技術でエキスを抽出して無味・無臭の製品にしたと
いう製品が市販されている。しかし、その製造技術の詳
細は明らかでない(川村賢司監修『なるほど・ザ・メキ
シカンアロエ』、四海書房、1986)。Since the extract of Chinese cabbage aloe has a strong bitterness and has a blue odor, it is difficult to use it as a folk medicine or health drink. Therefore, a product in which an extract is extracted from aloe by a special distillation technique to make it tasteless and odorless is commercially available. However, the details of its manufacturing technology are not clear (Kenji Kawamura's "Narudo the Mexican Aloe", Shikai Shobo, 1986).
【0004】[0004]
【発明が解決しようとする課題】そこで、アロエ抽出物
の苦味と青臭みを除いて、或いは抑制して、飲用し易い
飲料とすることを目的とした。鋭意研究の結果、本発明
の方法によって調製される物質をアロエ抽出液に加えて
風味を矯正することにより目的を達し得ることを発見
し、本発明を完成した。すなわち、本願は新たなアロエ
抽出物の風味矯正剤の製造方法を開示するものである。The object of the present invention is therefore to eliminate or suppress the bitterness and blue odor of the aloe extract to provide a drink that is easy to drink. As a result of earnest research, they have found that the substance prepared by the method of the present invention can be achieved by adding the substance to the aloe extract to correct the taste, and completed the present invention. That is, the present application discloses a method for producing a flavor-correcting agent of a new aloe extract.
【0005】[0005]
【課題を解決するための手段】本願のアロエ抽出物矯味
剤の製造方法は、基本的に以下のような各工程を結合す
ることから成る。 (イ)大豆粉砕物に米糠及びフィッシュミールを添加混
合して水抽出する工程 (ロ)水抽出液に糖質を加え、酵母菌を接種して醗酵さ
せる工程 (ハ)酵母醗酵液を加熱滅菌した後、乳酸菌を接種して
培養する工程 (ニ)乳酸菌培養液から有効成分を分離・精製する工程 以下、各工程ごとに詳細を説明する。The method for producing an aloe extract flavoring agent of the present application basically comprises combining the following steps. (B) Step of adding rice bran and fish meal to ground soybeans and extracting with water (b) Step of adding sugars to water extract and inoculating yeast with fermentation (c) Heat sterilizing yeast fermentation solution After that, the step of inoculating and culturing the lactic acid bacterium (d) The step of separating and purifying the active ingredient from the lactic acid bacterium culture solution will be described below in detail for each step.
【0006】(イ)大豆粉砕物に米糠及びフィッシュミ
ールを添加混合して水抽出する工程:丸大豆を適宜粉砕
したものを主要原料とする。本発明の目的には、脱脂大
豆粕または豆腐製造時のオカラも利用可能である。米糠
は、生糠または脱脂糠を使用する。フィッシュミール
は、鰯などを原料とした市販品のうち良質なものを使用
する。フィッシュミールの代わりに肉エキスや酵母エキ
スも使用することができる。これらの原料のうち、丸大
豆粉砕物、生糠、フィッシュミール等の脂肪含量は0.
8%(W/W)以下程度まで低下させたものが好まし
い。最終製品の矯味剤に“油焼け臭”が発生するのを避
けるためである。よって、丸大豆粉砕物、生糠、フィッ
シュミール等はあらかじめヘキサン等の溶剤で抽出処理
をしておく。脱脂大豆・脱脂米糠等の場合はそのまま使
用できる。(A) A step of adding rice bran and fish meal to a crushed soybean product and extracting with water: whole soybean is appropriately crushed as a main raw material. For the purpose of the present invention, defatted soybean meal or okara during the production of tofu can also be used. For rice bran, raw bran or defatted bran is used. For fish meal, use good quality commercial products made from sardines and the like. Meat extract or yeast extract can be used instead of fish meal. Of these raw materials, the fat content of crushed whole soybeans, raw rice bran, fish meal, etc. is 0.
It is preferably reduced to about 8% (W / W) or less. This is to avoid the occurrence of "oil burning smell" in the flavoring agent of the final product. Therefore, the crushed whole soybeans, raw rice bran, fish meal, etc. are extracted in advance with a solvent such as hexane. In the case of defatted soybean, defatted rice bran, etc., it can be used as it is.
【0007】原料の配合比は、大豆50部に対して米糠
20〜25部、フィッシュミール3〜10部とする。こ
れらを混合し、水を加えて全体を1000部とする。水
抽出の操作は、上記の混合物を15℃以下に24〜30
時間保持した後、懸濁物を濾別して行う。水抽出操作の
際の温度が、例えば室温程度(20〜30℃)に高くな
ると、抽出時に雑菌汚染が生じ易い。また、雑菌汚染の
生じ難い60℃以上の温度にすると、本願の目的の矯味
効果が低下するため、抽出温度は10〜15℃であるこ
とが望ましい。The mixing ratio of the raw materials is 20 to 25 parts of rice bran and 3 to 10 parts of fish meal to 50 parts of soybean. These are mixed and water is added to make 1000 parts. The operation of water extraction is carried out by heating the above mixture to 15 ° C or lower for 24 to 30
After holding for a time, the suspension is filtered off. When the temperature during the water extraction operation becomes high, for example, about room temperature (20 to 30 ° C.), contamination of various bacteria is likely to occur during extraction. Further, if the temperature is set to 60 ° C or higher at which contamination by bacteria is unlikely to occur, the taste masking effect for the purpose of the present application is lowered, so the extraction temperature is preferably 10 to 15 ° C.
【0008】(ロ)水抽出液に糖質を加え、酵母菌を接
種して醗酵させる工程:上記(イ)の工程で得た水抽出
液に糖質を5〜8%(W/W)加える。糖質としては、
蔗糖、ぶどう糖、果糖、麦芽糖など、酵母菌(サッカロ
ミセス・セレビッシェ)が利用し得るものならばいずれ
でもよい。糖質を添加した水抽出液を、110〜115
℃で20〜30分間加熱滅菌し、ついで、酵母菌(サッ
カロミセス・セレビッシェ)を接種して20〜25℃で
10〜12時間醗酵させる。使用するサッカロミセス・
セレビッシェ(Saccharomyces cerevisiae)は、清酒用
・製パン用等として市販されている菌株でよい。(B) Step of adding sugar to the water extract and inoculating yeast with the water to ferment: 5-8% (W / W) sugar in the water extract obtained in the step (a) Add. As a sugar,
Any sucrose, glucose, fructose, maltose, etc. that can be used by the yeast (Saccharomyces cerevisiae) may be used. Water extract containing sugar was added to 110-115.
The mixture is sterilized by heat at 20 ° C. for 20 to 30 minutes, then inoculated with yeast (Saccharomyces cerevisiae) and fermented at 20 to 25 ° C. for 10 to 12 hours. Saccharomyces used
The cerevisiae ( Saccharomyce s cerevisiae ) may be a commercially available strain for sake, bread making, etc.
【0009】(ハ)酵母醗酵液を加熱滅菌した後、乳酸
菌を接種して培養する工程:酵母菌による醗酵後、培養
液を75〜90℃で30分程度加熱して酵母菌を死滅さ
せる。ついで、死滅酵母菌体を除去することなく、この
培養液に乳酸菌を接種して培養する。使用する乳酸菌と
しては、ラクトバチルス・ブルガリカス(Lactobacillu
s delbrueckii subsp. bulgaricus )、ストレプトコッ
カス・サーモフィルス(Streptococcus salivarius sub
sp. thermophilus)、及び、ロイコノストック・メッセ
ンテロイデス(Leuconostoc mesenteroides )からなる
群の中の一種または二種以上の乳酸菌を用いる。これら
の菌株は、ヨーグルト製造用に市販されている菌株の中
から選ぶことができる。乳酸菌の培養は、培養液を18
〜20℃に24〜30時間保持した後、35〜40℃に
昇温して6〜7時間保持し、次いで10〜15℃に冷却
して72時間後醗酵を行って終了する。ここで、35〜
40℃の温度は本願で使用する乳酸菌群の増殖に好適な
温度範囲であり、10〜15℃は増殖速度が極めて遅い
温度範囲である。本願の目的の矯味性物質の本体は明ら
かではないが、乳酸菌培養時の温度管理は重要である。
醗酵終了後の培養液のpHは概ね4.3〜4.5とな
る。(C) Step of sterilizing the yeast fermentation broth by heating and then inoculating the lactic acid bacterium and culturing: After fermentation by the yeast, the culture broth is heated at 75 to 90 ° C. for about 30 minutes to kill the yeast. Then, the lactic acid bacterium is inoculated into this culture medium without removing the dead yeast cells and cultured. The lactic acid bacteria used are Lactobacillus
s delbruecki i subsp.bulgaricus ), Streptococcu s salivarius sub
sp. thermophilus ) and one or more lactic acid bacteria selected from the group consisting of Leuconostoc mesenteroides . These strains can be selected from the strains that are commercially available for yogurt production. For the cultivation of lactic acid bacteria, 18
After being kept at -20 ° C for 24 to 30 hours, the temperature is raised to 35 to 40 ° C and kept for 6 to 7 hours, then cooled to 10 to 15 ° C, and after 72 hours fermentation is completed. Where 35-
The temperature of 40 ° C. is a temperature range suitable for the growth of the lactic acid bacteria group used in the present application, and 10 to 15 ° C. is a temperature range in which the growth rate is extremely slow. Although the main body of the taste masking substance for the purpose of the present application is not clear, temperature control during culturing of lactic acid bacteria is important.
The pH of the culture solution after the fermentation is about 4.3 to 4.5.
【0010】(ニ)乳酸菌培養液から有効成分を分離・
精製する工程:乳酸醗酵終了後の培養液に20〜25%
(V/V)の低級アルコール類を加えて沈澱する区分を
濾別ないし遠心分離で除く。この上澄液に30〜35%
(V/V)の低級アルコール類を加えて沈澱する区分を
濾別ないし遠心分離で除く。この上澄液にさらに40〜
45%(V/V)の低級アルコール類を加えて沈澱する
区分を濾別ないし遠心分離で除く操作を繰り返してその
上澄液を採取する。ここで使用する低級アルコール類と
しては、メタノール、エタノール、プロパノール等いず
れも使用可能であるが、食品衛生上はエタノールが好ま
しい。(D) Separation of active ingredient from lactic acid bacterium culture solution
Purification step: 20-25% in the culture broth after the end of lactic acid fermentation
The (V / V) lower alcohols are added and the precipitated section is removed by filtration or centrifugation. 30-35% in this supernatant
The (V / V) lower alcohols are added and the precipitated section is removed by filtration or centrifugation. Add 40 to this supernatant.
A procedure in which 45% (V / V) lower alcohols are added and precipitates are removed by filtration or centrifugation is repeated to collect the supernatant. As the lower alcohols used here, any of methanol, ethanol, propanol and the like can be used, but ethanol is preferable in terms of food hygiene.
【0011】次いで上記のアルコール含有上澄液に硫酸
ナトリウムを15〜20%(W/W)加えて15〜20
分間静置後に濾別する。この沈澱区分をエタノールで洗
浄した後、水に再溶解し、透析ないしゲル濾過の手段で
硫酸ナトリウムを除く。以上の処理で得られた透析精製
液を真空乾燥ないし凍結乾燥の手段で乾燥して粉末と
し、本発明のアロエ抽出物矯味剤とする。収量は原料大
豆1キログラム当たり150〜200グラム程度であ
る。本品の1グラムは約1キログラムのキダチアロエ
(生葉)抽出物の苦味と青臭みを良くマスキングする効
果を有する。以下、実施例に基づいて更に詳細に説明す
る。Next, 15 to 20% (W / W) of sodium sulfate was added to the above alcohol-containing supernatant to obtain 15 to 20.
After standing for a minute, the mixture is filtered. After washing this precipitate with ethanol, it is redissolved in water and sodium sulfate is removed by means of dialysis or gel filtration. The dialyzed purified solution obtained by the above treatment is dried by means of vacuum drying or freeze-drying to give a powder, which is used as the aloe extract flavoring agent of the present invention. The yield is about 150 to 200 grams per kilogram of raw soybean. One gram of this product has the effect of masking the bitterness and blue odor of about 1 kilogram of the green leaf aloe extract. Hereinafter, the present invention will be described in more detail based on examples.
【0012】[0012]
実施例1:脱脂大豆500グラム、脱脂米糠200グラ
ム、および、フィッシュミール100グラムを混合し、
水を加えて10リットルにする。これを15℃に30時
間静置した後、濾過し、残滓に少量の水を加えて洗って
濾液10リットルを得た。該濾液に蔗糖500グラムを
加えて溶解し、20リットル容ジャーファーメンターに
入れて115℃、20分間滅菌し、25℃まで放冷した
後、サッカロミセス・セレビッシェの種培養液500ミ
リリットルを植菌し、25℃で12時間醗酵させた。Example 1: 500 grams of defatted soybeans, 200 grams of defatted rice bran, and 100 grams of fish meal were mixed,
Add water to make 10 liters. This was allowed to stand at 15 ° C. for 30 hours, then filtered, and a small amount of water was added to the residue to wash it to obtain 10 liters of a filtrate. 500 g of sucrose was added to the filtrate to dissolve it, and the mixture was placed in a 20 liter jar fermenter and sterilized at 115 ° C. for 20 minutes, allowed to cool to 25 ° C., and then inoculated with 500 ml of Saccharomyces cerevisiae seed culture solution. Fermentation was carried out at 25 ° C for 12 hours.
【0013】次いで該醗酵液を75℃まで昇温し30分
間保持して酵母菌を滅菌した後、20℃まで冷却し、ロ
イコノストック・メセンテロイデスの種培養液500ミ
リリットルを加えて20℃で30時間培養した後、40
℃まで昇温して6時間保持し、次いで10℃まで冷却し
て72時間後醗酵させた。醗酵終了後の培養液のpHは
4.3であった。該醗酵終了液にあらかじめ10℃に冷
却したエタノール2リットルを攪拌しながら加えて濾過
し、濾液にエタノール1リットルを追加し再濾過し、そ
の濾液にエタノール1リットルを追加し再濾過して、清
澄濾液12リットルを得た。Then, the fermentation liquor is heated to 75 ° C. and kept for 30 minutes to sterilize the yeast, then cooled to 20 ° C., 500 ml of a Leuconostoc mesenteroides seed culture broth is added, and the mixture is kept at 20 ° C. at 30 ° C. 40 hours after culturing
The temperature was raised to ℃ and held for 6 hours, then cooled to 10 ℃ and fermented after 72 hours. The pH of the culture broth after fermentation was 4.3. To the fermentation broth, 2 liters of ethanol cooled in advance to 10 ° C. was added with stirring and filtered, 1 liter of ethanol was added to the filtrate and refiltered, and 1 liter of ethanol was added to the filtrate and refiltered to clarify. 12 liters of filtrate were obtained.
【0014】該濾液12リットルに硫酸ナトリウム2キ
ログラムを加えて攪拌溶解し、20分間静置して生じた
沈澱を濾別した。該沈澱物を200ミリリットルの蒸留
水に溶解し、厚さ0.1mmのニトロセルロース膜を用
いて流水で20時間透析した。該透析液を常法により凍
結乾燥し、乾燥粉末85グラムを得た。この粉末0.5
グラムをキダチアロエの抽出液1リットルに添加して官
能試験を行ったところ、苦味・青臭みが大幅に解消され
た。2 kg of sodium sulfate was added to 12 liters of the filtrate, dissolved by stirring, and allowed to stand for 20 minutes, and the precipitate formed was separated by filtration. The precipitate was dissolved in 200 ml of distilled water and dialyzed against running water for 20 hours using a nitrocellulose membrane having a thickness of 0.1 mm. The dialysate was freeze-dried by a conventional method to obtain 85 g of dry powder. This powder 0.5
When 1 g of gram was added to 1 liter of extract of Kidachi aloe and a sensory test was conducted, bitterness and blue odor were largely eliminated.
【0015】実施例2:接種する乳酸菌として、実施例
1のロイコノストック・メセンテロイデスに代えてラク
トバチルス・ブルガリカス(Lactobacillus delbruecki
i subsp. bulgaricus )、及び、ストレプトコッカス・
サーモフィルス(Streptococcus salivarius subsp. th
ermophilus)の混合種培養液を接種し、実施例1と同様
に処理して乾燥粉末93グラムを得た。本品のキダチア
ロエ抽出物の苦味・青臭みに対するマスキング効果も、
ロイコノストック・メセンテロイデス使用の場合と相違
は認められなかった。Example 2: As a lactic acid bacterium to be inoculated, Lactobacillus bulgaricus ( Lactobacillus delbruecki) was used instead of the Leuconostoc mesenteroides of Example 1.
i subsp. bulgaricus ) and Streptococcus
Thermophilus ( Streptococcu s salivarius subsp. Th
ermophilus ) was inoculated and treated in the same manner as in Example 1 to obtain 93 g of dry powder. The masking effect against the bitterness and blue odor of the yellowtail aloe extract of this product,
No difference was observed with the use of Leuconostoc mesenteroides.
【0016】[0016]
【発明の効果】以上説明したように、本発明の製造方法
によって調製されたアロエ抽出物矯味剤をアロエ抽出物
に添加することにより、アロエ抽出物の有する苦味・青
臭みが大幅に減少されて、アロエ抽出物を民間薬ないし
健康食品として利用し易くする効果が認められる。As described above, by adding the aloe extract flavoring agent prepared by the production method of the present invention to the aloe extract, the bitterness and blue odor of the aloe extract are significantly reduced. , The effect of facilitating the use of aloe extract as a folk medicine or health food is recognized.
フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 //(C12P 1/02 C12R 1:865) (C12P 1/04 C12R 1:225 1:46 1:01) Continuation of the front page (51) Int.Cl. 6 Identification code Office reference number FI technical display area // (C12P 1/02 C12R 1: 865) (C12P 1/04 C12R 1: 225 1:46 1:01)
Claims (4)
矯味剤の製造方法。 (イ)大豆粉砕物に米糠及びフィッシュミールを添加混
合して水抽出する工程 (ロ)水抽出液に糖質を加え、酵母菌を接種して醗酵さ
せる工程 (ハ)酵母醗酵液を加熱滅菌した後、乳酸菌を接種して
培養する工程 (ニ)乳酸菌培養液から有効成分を分離・精製する工程1. A method for producing an aloe extract flavoring agent, which comprises combining the following steps. (B) Step of adding rice bran and fish meal to ground soybeans and extracting with water (b) Step of adding sugars to water extract and inoculating yeast with fermentation (c) Heat sterilizing yeast fermentation solution After that, the step of inoculating and culturing lactic acid bacteria (d) The step of separating and purifying the active ingredient from the lactic acid bacterium culture solution
レビッシェ(Saccharomyces cerevisiae)であることを
特徴とする請求項1記載のアロエ抽出物矯味剤の製造方
法。2. A process according to claim 1, wherein the aloe extract flavoring agent characterized by yeast is inoculated is Saccharomyces Serebisshe (Saccharomyce s cerevisiae).
ルガリカス(Lactobacillus delbrueckii subsp. bulga
ricus )、ストレプトコッカス・サーモフィルス(Stre
ptococcus salivarius subsp. thermophilus)、及び、
ロイコノストック・メッセンテロイデス(Leuconostoc
mesenteroides )からなる群の中の一種または二種以上
の乳酸菌であることを特徴とする請求項1記載のアロエ
抽出物矯味剤の製造方法。3. A lactic acid bacterium to be inoculated is Lactobacillus delbruecki i subsp. Bulga .
ricus ), Streptococcus thermophilus ( Stre
ptococcu s salivarius subsp. thermophilus ), and
Leuconostoc Mescenteroides
The method for producing an aloe extract flavoring agent according to claim 1, wherein the lactic acid bacterium is one kind or two or more kinds selected from the group consisting of mesenteroides ).
〜40℃)に保持した後、低温(10〜15℃)に保持
して後醗酵せしめることを特徴とする請求項1及び請求
項3記載のアロエ抽出物矯味剤の製造方法。4. A lactic acid bacterium culture solution is added to a lactic acid bacterium at an optimum growth temperature (35).
4. The method for producing an aloe extract flavoring agent according to claim 1 or 3, wherein the fermented aloe extract is held at a low temperature (10 to 15 ° C) for post-fermentation.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6334484A JPH08168388A (en) | 1994-12-19 | 1994-12-19 | Production of aloe extract flavor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6334484A JPH08168388A (en) | 1994-12-19 | 1994-12-19 | Production of aloe extract flavor |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH08168388A true JPH08168388A (en) | 1996-07-02 |
Family
ID=18277916
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6334484A Pending JPH08168388A (en) | 1994-12-19 | 1994-12-19 | Production of aloe extract flavor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH08168388A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1534815A1 (en) * | 2002-07-03 | 2005-06-01 | Ariake Japan Co. | Alcoholic beverages derived from animal extract, and methods for the production thereof |
JP2017513697A (en) * | 2014-04-11 | 2017-06-01 | ビュータマックス・アドバンスド・バイオフューエルズ・エルエルシー | Pollution reduction |
-
1994
- 1994-12-19 JP JP6334484A patent/JPH08168388A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1534815A1 (en) * | 2002-07-03 | 2005-06-01 | Ariake Japan Co. | Alcoholic beverages derived from animal extract, and methods for the production thereof |
EP1534815A4 (en) * | 2002-07-03 | 2005-09-21 | Ariake Japan Co | Alcoholic beverages derived from animal extract, and methods for the production thereof |
JP2017513697A (en) * | 2014-04-11 | 2017-06-01 | ビュータマックス・アドバンスド・バイオフューエルズ・エルエルシー | Pollution reduction |
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