JPS62146589A - Fermentation and production with gel containing embedded microorganism - Google Patents

Fermentation and production with gel containing embedded microorganism

Info

Publication number
JPS62146589A
JPS62146589A JP60286675A JP28667585A JPS62146589A JP S62146589 A JPS62146589 A JP S62146589A JP 60286675 A JP60286675 A JP 60286675A JP 28667585 A JP28667585 A JP 28667585A JP S62146589 A JPS62146589 A JP S62146589A
Authority
JP
Japan
Prior art keywords
fermentation
yeast
microorganism
stock solution
pva
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.)
Granted
Application number
JP60286675A
Other languages
Japanese (ja)
Other versions
JPH058669B2 (en
Inventor
Norio Nishikawa
西川 紀男
Kozo Kamata
鎌田 耕造
Masao Nanbu
南部 昌生
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sapporo Breweries Ltd
Eneos Corp
Original Assignee
Sapporo Breweries Ltd
Nippon Oil Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sapporo Breweries Ltd, Nippon Oil Corp filed Critical Sapporo Breweries Ltd
Priority to JP60286675A priority Critical patent/JPS62146589A/en
Publication of JPS62146589A publication Critical patent/JPS62146589A/en
Publication of JPH058669B2 publication Critical patent/JPH058669B2/ja
Granted legal-status Critical Current

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  • Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Distillation Of Fermentation Liquor, Processing Of Alcohols, Vinegar And Beer (AREA)

Abstract

PURPOSE:To shorten fermentation time and obtain a product in a high concentration having a good flavor, by blending polyvinyl alcohol (PVA) with the same fermentative solution as a fermentation stock solution, further adding a microorganism for fermentative production, repeatedly freezing and thawing the resultant mixture and using the resultant gel containing the embedded microorganism. CONSTITUTION:Polyvinyl alcohol (PVA) is added to the same fermentative solution as a stock solution to be fermented and dissolved while heating to give a fermentative solution containing the dissolved PVA, which is then cooled. A microorganism (yeast) for fermentative production is then added thereto to afford a mixed suspension, which is then injected and filled in a mold of a given shape and then subjected to freezing and thawing treatment at least twice to give a formed article, having good rubber-like elasticity and containing the embedded microorganism. The resultant formed article is then added to the above-mentioned stock solution to carry out fermentation. Since the stock solution suitable for cultivation of the yeast is previously contained in the gel, the yeast is directly ingested as a nutriment to carry out multiplication and the aimed fermentation product of good quality is obtained in a short time.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、産業用、研究用などに利用し得る微生物包埋
ゲルによる発酵生産法。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention is a fermentation production method using microorganism-embedded gel that can be used for industrial and research purposes.

(従来の技術) 出願人は先に、ポリビニルアルコール(PVA)粉末を
水に加熱溶解し、その水溶液に微生物を混入させた混合
懸濁液に、凍結・解凍を反復してゴム状弾性を有する微
生物包埋ゲルを製造すること、並にこの場合、凍結に先
立ち、微生物の凍結障害を回避する目的でグリセリン、
ゼラチン、澱粉、などの凍fll!i障害保護剤を添加
することを特開昭57−141291号、特開昭29−
56446号その伯で開示した。
(Prior Art) The applicant first heated and dissolved polyvinyl alcohol (PVA) powder in water, mixed microorganisms into the aqueous solution, and made a mixed suspension that had rubber-like elasticity by repeatedly freezing and thawing it. To prepare a microorganism-embedded gel, and in this case, prior to freezing, glycerin,
Freeze gelatin, starch, etc.! The addition of an i-damage protectant is disclosed in JP-A-57-141291 and JP-A-29-Sho.
Disclosed in No. 56446.

(発明が解決しようとする問題点) 上記従来の凍結障害防止剤を添加しないでPVA−微生
物の混合懸濁液を凍結・解凍を反復してゴム状弾性のゲ
ルとする場合は、微生物の1部が死滅ないし弱化するこ
とが認められた。
(Problems to be Solved by the Invention) When a mixed suspension of PVA and microorganisms is repeatedly frozen and thawed to form a rubber-like elastic gel without adding the above-mentioned conventional anti-freezing agent, it is necessary to It was observed that some parts of the body died or weakened.

従ってこのゲルを用いて例えばビールの発酵生産のため
、その原液である麦芽汁を発酵さぜるときは、発酵の定
常状態が19られるまでに艮時問を要し、その上ゲルの
多量の添加により、麦芽汁の濃度がそれたけ希釈され、
生産されるアルコールの濃度は低下し、そのまま生産品
として供し1qない無駄を生ずる不都合をもたらす。
Therefore, when using this gel to ferment wort, which is the stock solution, for fermentation production of beer, it takes a long time to reach a steady state of fermentation, and in addition, a large amount of gel is used. By adding, the concentration of wort is diluted by that amount,
The concentration of the alcohol produced decreases, resulting in the inconvenience that less than 1 q of alcohol is wasted if it is used as a product as it is.

前記の凍結障害防止剤を添加してPVA−微生物の混合
懸濁液を凍結・解凍を反復してゴム状弾性のゲルとする
場合は、微生物の死滅及び弱化は防止されるが、ビール
の発酵生産に使用したとき、前記の障害防止剤は、麦芽
汁とは異質の物質であるので、不純で風味や品質の劣化
したビールをもたらす等の不都合を伴う。
When the above-mentioned anti-freezing agent is added and the mixed suspension of PVA and microorganisms is repeatedly frozen and thawed to form a rubber-like elastic gel, the death and weakening of the microorganisms are prevented, but beer fermentation is prevented. When used in production, the anti-damage agent is a substance different from the wort, and therefore has disadvantages such as producing beer that is impure and has a deteriorated flavor and quality.

(問題点を解決するための手段) 本発明は、発酵時間を短縮し且つアルコールや乳酸、酢
酸などの発酵生産物の濃度の向上した発酵を行なうこと
ができる微生物包埋ゲルによる発酵生産法を提供するも
ので、原料ポリビニルアルコール(PVA)と発酵原液
と同じ発酵性液とを混合したものを加熱♂解し、得られ
たPVA ?fJ解発酵性液を冷却しこれに発酵生産用
微生物を添加して生る混合懸濁液に、凍結・解凍を反復
して微生物包埋ゲルを製造し、該微生物包埋ゲルにより
前記発酵させるべき原液を光醇させることを特徴とする
(Means for Solving the Problems) The present invention provides a fermentation production method using microorganism-embedded gel that can shorten fermentation time and perform fermentation with improved concentrations of fermentation products such as alcohol, lactic acid, and acetic acid. What we offer is PVA obtained by heating and melting a mixture of raw material polyvinyl alcohol (PVA) and the same fermentable liquid as the fermentation stock solution. A mixed suspension produced by cooling the fJ defermentable liquid and adding microorganisms for fermentation production thereto is repeatedly frozen and thawed to produce a microorganism-embedded gel, and the microorganism-embedded gel is used for the above-mentioned fermentation. It is characterized by making the undiluted solution brighter.

(実施例) 次に本発明の詳細な説明する。(Example) Next, the present invention will be explained in detail.

原料、ポリビニルアルコール(PVA)は、けん化度9
5モル%以上、平均重合度700以上を有するものとし
、例えばその粉末を6v1t%以上を、発酵すべき原液
と同じ発酵性液に添加し加熱溶解し、PVA溶解溶解発
液性液る。例えばビール製造においては、発酵すべき原
料は麦芽汁であるので、該PVAの溶媒としての発酵性
液は、麦芽汁を使用する。かくしてPVA溶解麦芽汁に
適量の圧Pl!酵母を5〜10wt%添加して、混合懸
濁液を調製し、これを所定形状の生形用鋳型内に所望量
注入充填し、これを冷凍庫内で一3°以下、例えば−2
0℃に凍結させ、次に外部に出し、至温で解凍する。再
び上記の凍結処理を施し、凍結・解凍を少なくとも2回
行なう。
The raw material, polyvinyl alcohol (PVA), has a saponification degree of 9.
5 mol % or more and an average degree of polymerization of 700 or more. For example, 6 vol 1 t % or more of the powder is added to the same fermentable liquid as the stock solution to be fermented and dissolved by heating to form a PVA-dissolved liquefying liquid. For example, in beer production, the raw material to be fermented is wort, so wort is used as the fermentable liquid as a solvent for the PVA. In this way, the appropriate amount of pressure Pl is applied to the PVA-dissolved wort! Add 5 to 10 wt% of yeast to prepare a mixed suspension, inject and fill the desired amount into a green mold with a predetermined shape, and store this in a freezer at a temperature of -3° or less, e.g. -2
Freeze it to 0°C, then take it outside and thaw it at the lowest temperature. The above freezing treatment is performed again, and freezing and thawing are performed at least twice.

麦芽汁中のPVAの濃度は、6〜25wt%の範囲がよ
い。この範囲において、良好なゴム状弾性を有する微生
物包埋ゲルの成形体が1qられる。
The concentration of PVA in the wort is preferably in the range of 6 to 25 wt%. Within this range, 1 q of molded microorganism-embedded gel having good rubber-like elasticity is obtained.

麦芽汁の濃度は、ビール製造における発酵原液である麦
芽汁と同じでよい。勿論それ以上の1度のものでも差支
えない。必要に応じ、これにグルコース、酵母エキスな
どビール醸造に差支えない異臭、異味のない栄養成分を
少量添加するようにしてもよい。
The concentration of wort may be the same as that of wort, which is the fermentation stock solution used in beer production. Of course, there is no problem with a one-time event more than that. If necessary, a small amount of nutritional components such as glucose and yeast extract that do not interfere with beer brewing and have no off-odor or off-taste may be added thereto.

上記によって凍結・解凍を3回繰り返して1qられた麦
芽汁を含む酵母包埋グル成形体につき、その包埋酵母の
生理活性を2型染色式弱化度測定法(西用紀男: In
5t、 Brewing、 Proc、13thCon
v、105(1974) )により測定した所、健全酵
母は全体の85%、やや弱化した酵母は15%であり、
死滅酵母と弱化酵母は全く認められなかった。比較のた
め、溶媒として水のみを使用して同様に作成した酵母包
埋ゲル成形体につき、仝法により測定した所、健全酵母
は全体の55%、やや弱化した酵母は25%、弱化酵母
15%、死滅酵母5%であった。
For the yeast-embedded glu molded body containing 1q of wort obtained by repeating freezing and thawing three times as described above, the physiological activity of the embedded yeast was measured using the type 2 staining method for measuring the degree of weakening (Norio Nishiyo: In
5t, Brewing, Proc, 13thCon
According to the measurements made by J. V., 105 (1974), healthy yeast accounted for 85% of the total and slightly weakened yeast accounted for 15%.
No dead yeast or weakened yeast was observed. For comparison, a yeast-embedded gel molded body similarly prepared using only water as a solvent was measured using the same method, and 55% of the total was healthy yeast, 25% was slightly weakened yeast, and 15% was weakened yeast. %, and 5% dead yeast.

上記本発明により得た麦芽汁含有酵母包埋ゲル成形体を
ビール醸造における麦芽汁の発酵に当り、その発酵タン
ク内に、適宜の大きさに截断したものを所望個数設置し
、バッチ式或は連続式で麦芽汁の発酵を行なった所、ゲ
ル中の酵母が発酵の定常状態まで増殖するまでに要する
日数は、上記比較用に作成したゲル中の酵母が定常状態
まで増殖するまでに要する日数より数日早くなることが
認められ、それだけ早期に発酵生産を完了した。これは
、本発明のゲル中に予め酵母の培養に適した麦芽汁が予
め含有されて居るので、包埋酵母は直ちにこれを栄養分
として摂取し直ちに増殖し得られるからである。
When fermenting wort in beer brewing, the wort-containing yeast-embedded gel molded body obtained according to the present invention is cut into a desired size and placed in a fermentation tank in a desired number, and batch-type or When fermenting wort in a continuous manner, the number of days required for the yeast in the gel to grow to a steady state of fermentation is the number of days required for the yeast in the gel created for the above comparison to grow to a steady state. It was recognized that the process was several days earlier, and the fermentation production was completed earlier. This is because the gel of the present invention already contains wort suitable for culturing yeast, so the embedded yeast can immediately ingest this as nutrients and proliferate immediately.

これに対し、上記比較のゲルではその包埋酵母は、当初
、何等栄養のない水で囲まれて居るので、直ちに増殖す
ることができず、外部の発酵せしめるべき麦芽汁が侵入
しこれを栄養として増殖するまでに長時間を要するから
であると考えられる。この場合、本発明によれば、その
酵母の培養液として、特に、発酵せしめるべき原液と同
じ材料、即ち、ビール発酵生産の場合は、麦芽汁を使用
したので、発酵せしめるべき原液である麦芽汁と同様の
同じ発酵環境に始めから包埋酵母を馳しませられるので
、酵母の発酵条件を常に良好で且つ均一に維持でき且つ
風味の損なわないビールが円滑に得られる。従って、酵
母の栄養分とはなるが、その発酵せしめるべき原液、上
記の例では麦芽汁と異なる材料から成る凍結障害防止剤
をゲル中に含有する場合のような、発酵原液に対し不純
物となる或は発酵生産物、上記の例ではビールの品質、
風味を汚損することがなく、有利であり、而も、そのゲ
ル中に含まれる麦芽汁分に対応してアルコール発酵、乳
酸発酵等の発酵生産量を向上できる。これに対し、水の
みをPVAの溶媒として使用して作成した包埋酵母ゲル
を使用した場合、その水分含有量だけ希釈された発酵生
産物をもたらし、特にビール等の発酵飲料等の生産には
不適である。
On the other hand, in the comparative gel described above, the embedded yeast is initially surrounded by water with no nutrients, so it cannot proliferate immediately, and the wort to be fermented from outside enters and nourishes it. This is thought to be due to the fact that it takes a long time to proliferate. In this case, according to the present invention, the same material as the stock solution to be fermented is used as the culture solution for the yeast, that is, in the case of beer fermentation production, wort is used. Since the embedded yeast can be incubated in the same fermentation environment from the beginning, the yeast fermentation conditions can always be kept good and uniform, and beer without loss of flavor can be smoothly obtained. Therefore, although it provides nutrients for the yeast, it may also become an impurity in the fermentation stock solution, such as when the gel contains a freeze damage prevention agent made of a material different from the wort in the above example. is the fermentation product, in the above example the quality of the beer,
It is advantageous because it does not spoil the flavor, and furthermore, the yield of fermentation such as alcoholic fermentation and lactic acid fermentation can be improved corresponding to the wort content contained in the gel. In contrast, the use of an embedded yeast gel made using only water as a solvent for PVA results in a fermentation product that is diluted by its water content, which is particularly difficult for the production of fermented beverages such as beer. Not suitable.

次に更に具体的な実施例につき説明する。Next, more specific examples will be described.

実施例1 容器内にPVA粉末1!iogと11°B(]麦芽汁8
50戒を加え、これをオートクレーブにより 121℃
で15分間加熱し、PVA溶解発酵性液を1qた。これ
を窄温まで冷lJシた後これに圧搾ビール酵母1003
を添加し、攪拌して得た混合懸濁液を、皿状の平板容器
に流し込み、厚さ 7Nnの薄層とし、これを冷凍庫内
に収容し、−20℃に凍結後、取り出し至温で解凍した
。この凍結・解凍処理をその後2回、合計3回行ない、
ゴム状弾性の酵母包埋ゲル成形板を得た。このゲル成形
体につき、包埋酵母の生理活性を検べた所、死滅酵母、
弱化酵母は全く存在せず、健全酵母90%、やや弱化酵
lm110%の分布であった。このビール酵母包埋ゲル
の截断片200 gを500m1容シリンダーに入れ、
11°Bg麦芽汁300m1を加え、15℃、48時間
発酵させ、以後は24時間毎に11°B(1麦芽汁を入
れ替え、発酵の定常状態が得られる迄の時間を測定した
所、麦芽汁3回人机替え4日目に定常状態を得た。比較
のため、水のみを溶媒として上記と同じ方法で作成した
ビール酵母包埋ゲルの截断片2009を500d容シリ
ンダーに入れ、11°BCI麦芽汁300dを加え、以
下上記と同様に麦芽汁の入れ替えを行ない発酵を行なっ
た場合、発酵が定常状態になるまでには、麦芽汁を5回
入れ替え、6日目に定常状態を得た。
Example 1 One piece of PVA powder in the container! iog and 11°B (] wort 8
Add 50 precepts and autoclave at 121℃
The mixture was heated for 15 minutes, and 1 q of PVA-dissolved fermentable liquid was obtained. After cooling this to a narrow temperature, add pressed beer yeast 1003 to this.
The mixed suspension obtained by adding and stirring was poured into a dish-shaped flat plate container to form a thin layer with a thickness of 7Nn, which was placed in a freezer and frozen at -20°C, then taken out and kept at room temperature. Unzipped. This freezing/thawing process was then carried out twice, for a total of three times.
A rubber-like elastic yeast-embedded gel molded plate was obtained. When this gel molded body was tested for the physiological activity of the embedded yeast, it was found that dead yeast,
There was no weakened yeast at all, and the distribution was 90% healthy yeast and 110% slightly weakened yeast. Put 200 g of the cut pieces of this brewer's yeast embedding gel into a 500 ml cylinder,
300ml of 11°Bg wort was added and fermented at 15°C for 48 hours. After that, 11°Bg wort was replaced every 24 hours (one wort was replaced, and the time until a steady state of fermentation was reached was measured. Steady state was obtained on the 4th day after three personnel changes.For comparison, a cut piece of beer yeast embedding gel 2009 prepared in the same manner as above using only water as a solvent was placed in a 500 d cylinder and incubated at 11° BCI. When 300 d of wort was added and fermentation was carried out by replacing the wort in the same manner as above, the wort was replaced 5 times until the fermentation reached a steady state, and a steady state was achieved on the 6th day.

このように、本発明の酵母包埋ゲルにより発酵時間を短
縮できる。
Thus, the fermentation time can be shortened by the yeast-embedded gel of the present invention.

又、本発明の上記酸m包埋ゲルを使用して4回目の定常
状態において、アルコール4.8%含有のビール発酵液
が得られたに対し、上記の比較酵母包埋ゲルを使用した
場合、当初の発酵液中のアルコール含有量は2.5%に
すぎなかった。
In addition, in the fourth steady state using the acid m-embedded gel of the present invention, a beer fermentation liquid containing 4.8% alcohol was obtained, whereas when the comparative yeast-embedded gel was used. The alcohol content in the initial fermentation liquid was only 2.5%.

而して麦芽汁の3回目の置換でも、発酵液中のアルコー
ル含有量は所要の48%に遅せず開渠しなければならな
い無駄を生じた。
Even after replacing the wort for the third time, the alcohol content in the fermented liquid was reduced to the required 48%, which resulted in waste, as the drain had to be opened without delay.

実施例2 培苺液として15%廃糖密850dとP■△粉末150
9とを入れた容器を7t−1〜クレープで加熱溶解し、
冷mls、cereviside var、cllip
soideus At1U 3200 (サツカロミセ
ス、セレビシェ バリアント エリブソイデウス エイ
エイチュー3200 )の圧Pi8菌体100Jを加え
よく攪拌混合して14た混合懸濁液を、平板容器に流し
、次で冷凍庫内入れ、実施例1と同様に冷凍・解凍を3
回反復して、酵母包埋グル成形薄板を得た。これを7x
 7X  7ttry、の立方形に截断し、その截断片
800 gを15%廃糖密1000mに加え、30℃、
24時間発酵させ、5.5wt%のアルコール発酵液を
得た。
Example 2 15% waste molasses 850d and P■△ powder 150d as cultivated strawberry liquid
Heat and melt the container containing 9 with 7t-1 ~ crepe,
cold mls, cereviside var, clip
Add 100 J of pressure Pi8 microbial cells of E. soideus At1U 3200 (Satsucharomyces, cerevisiae variant Erybusoideus AT1U 3200) and mix thoroughly with stirring. The mixed suspension was poured into a flat plate container, and then placed in the freezer, as in Example 1. Freeze and thaw 3 times.
The process was repeated several times to obtain yeast-embedded glue molded thin plates. 7x this
Cut into cubes of 7×7ttry, add 800 g of the cut pieces to 1000 m of 15% waste molasses, and heat at 30°C.
Fermentation was performed for 24 hours to obtain a 5.5 wt % alcoholic fermentation liquid.

比較のため、溶媒として水850rdを使用し、その他
は、前記実施例2と同様にして作成した酵母包埋ゲル成
形薄板の同じ大きさの立方形成断片800gを15%廃
糖蜜1000dに加えて30℃で発酵させた所、3日間
経過しても3wt%のアルコール発酵液を得るにとどま
った。
For comparison, 850 rd of water was used as the solvent, and 800 g of cube-formed pieces of the same size of the yeast-embedded gel molded thin plate prepared in the same manner as in Example 2 were added to 1000 d of 15% blackstrap molasses for 30 g. When fermentation was carried out at ℃, only 3 wt% alcohol fermentation liquid was obtained even after 3 days.

実施例3 容器内に、麦芽10007とこれに対しPVA扮末15
%を入れ、オートクレーブで加熱溶解した後至温に冷却
し、これに、予め通常の前培養を行ない遠心分離により
集菌した乳酸菌り、dclbrueckii  (ラク
トバチルス・デルブリュッキー)の集菌菌体を加えて得
た調製液を、これを平板容器に流し、冷凍庫で一25℃
での凍結と空窩での解凍を3回繰り返して乳酸菌包埋ゲ
ル成形体を(qた。これを立方形に細断して得た多数個
を、800g10’ B麦芽汁1ooo#li!に加え
42℃、24時間発発酵せ、乳M! 1.2%含有の発
酵液を得た。
Example 3 In a container, malt 10007 and PVA dressing powder 15
%, heated and dissolved in an autoclave, cooled to a very low temperature, and collected bacterial cells of lactic acid bacteria, dclbrueckii, which had been precultured in advance and collected by centrifugation. Pour the prepared solution into a flat container and store it in the freezer at -25°C.
The process of freezing and thawing in the cavity was repeated three times to obtain a lactic acid bacteria-embedded gel molded body (q).Cut this into cubes and make a large number of pieces into 800g10' B wort 1ooo#li! The mixture was added and fermented at 42°C for 24 hours to obtain a fermented liquid containing 1.2% Milk M!.

比較のため、麦芽汁に代え、水1ooordをPV^溶
媒として使用し、前記実施例3と同様にして乳酸菌包埋
ゲル成形体を得た。
For comparison, a lactic acid bacteria-embedded gel molded body was obtained in the same manner as in Example 3 except that 100 ml of water was used as the PV solvent instead of wort.

これにつき、前記実施例3に記載と同様に乳酸発酵させ
た所、3日間の発酵では、僅が0.3%程度の乳酸含有
の発酵液が得られたにすぎなかった。
Regarding this, when lactic acid fermentation was carried out in the same manner as described in Example 3, a fermented liquid containing only about 0.3% lactic acid was obtained after 3 days of fermentation.

実施例4 乳酸菌としてBiridobacterium(ビフィ
ドバクテリウム)を実施例3と同様に培養し、集菌した
菌体を使用する以外は、実施例3と同様に包埋グル成形
体の作成と、乳酸発酵を行なった所、乳酸143%の濃
度の乳酸発酵液を得た。
Example 4 Biridobacterium was cultured as lactic acid bacteria in the same manner as in Example 3, and an embedded glue molded body was created and lactic acid fermentation was carried out in the same manner as in Example 3, except that the collected bacterial cells were used. As a result, a lactic acid fermentation liquid with a lactic acid concentration of 143% was obtained.

(発明の効果) このように本発明によるときは、PVへの溶媒として、
発酵させるべき原液と同じ発酵性液を使用してその発酵
微生物の包埋ゲルを作成し、このゲルを使用し、該発酵
させるべき原液を発酵させるようにしたので、発酵時間
を短縮し得られ且つ高濃度のアルコール、乳酸等の所要
の発酵生産成分を含む良質の発酵液の生産を確実にもた
らす等の効果を特する 特許 出 願 人 日本石油株式会社 外2名 手続補正書 16事件の表示 昭和60年特許願第286675号 2、発明の名称 微生物包埋ゲルによる発酵生産法 3補正をする者 事件との関係 特許出願人 日本石油株式会社 サッポロビール株式会社 4、代 理 人 ?lt話503〜1811番(代)?−−−・5、補正
命令の日付(自発) & 補正の対象 明細書の発明の詳細な説明の欄 7、補正の内容 (1)明細書第2頁第2行の「発酵生産法。」を「発酵
生産法に関する。」と訂正する。
(Effect of the invention) As described above, according to the present invention, as a solvent for PV,
By using the same fermentable solution as the stock solution to be fermented, we created a gel embedding the fermenting microorganisms, and using this gel to ferment the stock solution to be fermented, the fermentation time could be shortened. A patent that has the effect of reliably producing a high-quality fermented liquid containing necessary fermentation production components such as high concentrations of alcohol and lactic acid.Applicant: 2 persons other than Nippon Oil Co., Ltd.Representation of procedural amendment case 16 Patent Application No. 286675 of 1985 2, Name of the invention Fermentation production method using microorganism-embedded gel 3 Relationship to the case of the person making the amendment Patent applicant Nippon Oil Co., Ltd. Sapporo Breweries Ltd. 4, agent? Lt story 503-1811 (generation)? ---・5. Date of amendment order (voluntary) & Detailed explanation of the invention in the specification subject to amendment 7, Contents of amendment (1) "Fermentation production method" on page 2, line 2 of the specification. is corrected to "Relates to fermentation production methods."

(2)  同省第2頁第10行の「澱粉、など」を「澱
粉など」と訂正する。
(2) "Starch, etc." in line 10 of page 2 of the ministry is corrected to "starch, etc."

(3)  同書第3頁第20行の「生る」を「生じる」
と訂正する。
(3) "Arise" for "to live" in line 20, page 3 of the same book.
I am corrected.

(4)同書第4頁第8行の「粉末を6 wt%」を「粉
末6 wt%」と訂正する。
(4) In the same book, page 4, line 8, "6 wt% powder" is corrected to "6 wt% powder."

(5)同書第4頁第15行の「生形用」を「成形用」と
訂正する。
(5) "For raw shapes" on page 4, line 15 of the same book is corrected to "for molding."

(6)同書第5頁第17行の「仝」を「同」と訂正する
(6) In the same book, page 5, line 17, "仝" is corrected to "same".

(7)同書第6頁第3行乃至第4行の「裁断」を「裁断
」と訂正する。
(7) "Cut" in lines 3 and 4 of page 6 of the same book is corrected to "cut".

(8)  同書第6頁第13行の「増殖し得られる」を
「増殖できる」と訂正する。
(8) In the same book, page 6, line 13, "can multiply" is corrected to "capable of multiplying."

(9)同書第7頁第6行の「損なわない」を「損なわれ
ない」と訂正する。
(9) In the same book, page 7, line 6, ``not impair'' is corrected to ``not be impaired.''

<1(l  同書第8頁第15行の「裁断片」を「裁断
片」と訂正する・ αυ 同書第9頁第2行の「裁断片」を「裁断片」と訂
正する。
<1 (l Correct "shredded fragments" in line 15 of page 8 of the same book as "shredded fragments" - αυ Correct "shredded fragments" in line 2 of page 9 of the same book as "shredded fragments".

■ 同書第9頁第20行の「cereviside J
を(−cerevisi&e Jと訂正する。
■ "cereviside J" on page 9, line 20 of the same book.
is corrected as (-cerevisi&e J.

CI)  同省第10頁第5行の「内入れ」を「に入れ
」と訂正する。
CI) In line 5 of page 10 of the Ministry, "inner" is corrected to "inere."

@ 同省第10頁第7行の「截断し、その截断」を「裁
断し、その裁断」と訂正する。
@ The Ministry of Justice, page 10, line 7, ``cut and cut'' is corrected to ``cut and cut.''

の 同書@10頁第13行乃至第14行の「裁断片」を
「裁断片」と訂正する。
In the same book, page 10, lines 13 and 14, "shredded fragment" is corrected to "shredded fragment".

04)  同書第11頁第3行の「集菌菌体を加えて得
た調製液を、これを平板」を「菌体を加えて得た調製液
を平板」と訂正する。
04) In the same book, page 11, line 3, ``The prepared liquid obtained by adding collected bacterial cells is plated'' is corrected to ``The prepared liquid obtained by adding bacterial cells is plated.''

(2つ  同書第11頁第3行の「細断」を「裁断」と
訂正する。
(2) "Shred" in line 3 of page 11 of the same book is corrected to "shred."

Claims (1)

【特許請求の範囲】 1、原料ポリビニルアルコール(PVA)と発酵原液と
同じ発酵性液とを混合したものを加熱溶解し、得られた
PVA溶解発酵性液を冷却しこれに発酵生産用微生物を
添加して成る混合懸濁液に、凍結・解凍を反復して微生
物包埋ゲルを製造し、該微生物包埋ゲルにより前記発酵
させるべき原液を発酵させることを特徴とする微生物包
埋ゲルによる発酵生産法。 2、発酵原液及び発酵性液は麦芽汁である特許請求の範
囲1に記載のアルコール又は乳酸の発酵生産法。 3、発酵原液及び発酵性液は廃糖密水溶液である特許請
求の範囲1に記載のアルコールの発酵生産法。
[Claims] 1. A mixture of raw material polyvinyl alcohol (PVA) and the same fermentable liquid as the fermentation stock solution is heated and dissolved, the obtained PVA-dissolved fermentable liquid is cooled, and microorganisms for fermentation production are added to it. A microorganism-embedded gel is produced by repeatedly freezing and thawing a mixed suspension obtained by adding the above-mentioned ingredients, and the raw solution to be fermented is fermented by the microorganism-embedded gel. Production method. 2. The method for fermentative production of alcohol or lactic acid according to claim 1, wherein the fermentation stock solution and fermentable liquid are wort. 3. The method for fermentative production of alcohol according to claim 1, wherein the fermentation stock solution and the fermentable liquid are waste sugar dense aqueous solutions.
JP60286675A 1985-12-19 1985-12-19 Fermentation and production with gel containing embedded microorganism Granted JPS62146589A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60286675A JPS62146589A (en) 1985-12-19 1985-12-19 Fermentation and production with gel containing embedded microorganism

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60286675A JPS62146589A (en) 1985-12-19 1985-12-19 Fermentation and production with gel containing embedded microorganism

Publications (2)

Publication Number Publication Date
JPS62146589A true JPS62146589A (en) 1987-06-30
JPH058669B2 JPH058669B2 (en) 1993-02-02

Family

ID=17707507

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60286675A Granted JPS62146589A (en) 1985-12-19 1985-12-19 Fermentation and production with gel containing embedded microorganism

Country Status (1)

Country Link
JP (1) JPS62146589A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013524827A (en) * 2010-04-27 2013-06-20 クリスチャン・ハンセン・アクティーゼルスカブ Method for inoculating yeast into fruit juice

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS541501A (en) * 1977-06-04 1979-01-08 Japanese National Railways<Jnr> Training simulator for operating motive power
JPS5847492A (en) * 1981-09-14 1983-03-19 Nippon Oil Co Ltd Immobilization and propagation of mold of microorganism

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS541501A (en) * 1977-06-04 1979-01-08 Japanese National Railways<Jnr> Training simulator for operating motive power
JPS5847492A (en) * 1981-09-14 1983-03-19 Nippon Oil Co Ltd Immobilization and propagation of mold of microorganism

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013524827A (en) * 2010-04-27 2013-06-20 クリスチャン・ハンセン・アクティーゼルスカブ Method for inoculating yeast into fruit juice
JP2016039816A (en) * 2010-04-27 2016-03-24 クリスチャン・ハンセン・アクティーゼルスカブChr. HansenA/S Method for inoculating yeast into fruit juice

Also Published As

Publication number Publication date
JPH058669B2 (en) 1993-02-02

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