JPS62259576A - Fermentation apparatus - Google Patents

Fermentation apparatus

Info

Publication number
JPS62259576A
JPS62259576A JP61103415A JP10341586A JPS62259576A JP S62259576 A JPS62259576 A JP S62259576A JP 61103415 A JP61103415 A JP 61103415A JP 10341586 A JP10341586 A JP 10341586A JP S62259576 A JPS62259576 A JP S62259576A
Authority
JP
Japan
Prior art keywords
culture
tank
raw material
fermentation
material liquid
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
Application number
JP61103415A
Other languages
Japanese (ja)
Inventor
Kyozo Kawachi
河内 恭三
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.)
Toshiba Corp
Original Assignee
Toshiba 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 Toshiba Corp filed Critical Toshiba Corp
Priority to JP61103415A priority Critical patent/JPS62259576A/en
Publication of JPS62259576A publication Critical patent/JPS62259576A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To shorten the time necessary for acclimatization and to continue high productivity of fermentation product preventing metabolic inhibition, by connecting a culture tank with a filter to separate a culture liquid into fermentation cells and a fermentation product and with a membrane-type reactor having a membrane to divide the space in the reactor for feeding a raw material liquid to the culture liquid. CONSTITUTION:The space in a membrane-type reactor 1 is divided with a partition membrane 14 into a culture liquid chamber 12 and a raw material liquid chamber 13. The culture liquid chamber 12 is connected to a culture tank 16 through pipes 15a, 15b to circulate the culture liquid. The raw material liquid chamber 13 is connected to a raw material tank 18 through pipes 15c, 15d to enable the circulation of the raw material liquid. The culture tank 16 is connected with an aseptic water tank 22 through a pipe 15e to be fed with aseptic water. The culture tank 16 is connected with a filter 23 through pipes 15f, 15g and the fermented liquid is separated with the filter 23 into a fermentation product and fermenting bacterial cells. The latter component is returned to the culture tank 16 and the former component is collected as the objective product.

Description

【発明の詳細な説明】 [発明の目的] (産業上の利用分野) 本発明は、例えば味噌や醤油などのf11id食品を製
造するための醗酵装置の改良に関する。
DETAILED DESCRIPTION OF THE INVENTION [Object of the Invention] (Industrial Field of Application) The present invention relates to improvements in fermentation equipment for producing flid foods such as miso and soy sauce.

(従来の技術) 従来の醗酵装置としては、第2図に示すv4造のものが
知られている。即ち、図中の1は原料槽、2は培養槽、
3.4はポンプ、5は醗酵槽である。
(Prior Art) As a conventional fermentation apparatus, a V4 type fermentation apparatus shown in FIG. 2 is known. That is, 1 in the figure is a raw material tank, 2 is a culture tank,
3.4 is a pump, and 5 is a fermentation tank.

こうした醗酵装置により醗酵食品を製造するには、前記
原料槽1に麹菌により予め消化させた原料液を、培養槽
2にtlill菌(酵母菌や乳酸菌)を高濃度に培養し
た培養液を夫々貯蔵し、原料液及び培養液をポンプ3.
4によりl酸槽5に供給し、撹拌しながら1〜3か月醗
酵する方法が採用されている。
In order to produce fermented foods using such a fermentation device, a raw material liquid pre-digested by Aspergillus oryzae is stored in the raw material tank 1, and a culture liquid obtained by culturing trill bacteria (yeast bacteria and lactic acid bacteria) at a high concentration is stored in the culture tank 2. 3. Pump the raw material solution and culture solution.
4 to the acid tank 5 and fermentation is carried out for 1 to 3 months while stirring.

上述した醸M@画においては、一般に第3図に示す特性
を持つ異種の醗酵反応が引続いて起きる。
In the above-mentioned fermentation process, different types of fermentation reactions generally occur subsequently, having the characteristics shown in FIG.

第3図において、横軸は時間、縦軸は濃度、曲線Aは醗
酵生成物濃度(例えばアルコール濃度)、曲線Bは醗酵
菌濃度(例えば酵母菌濃度)、曲線Cは残余基質濃度(
例えばグル°コース濃度)である。[醗酵菌濃度は、植
種(t−0)の後馴養期(tl)を過ぎて、対数増殖期
(1+〜t2)に入り、急激に高くなる。同時に基質I
ltが低下し、allll酸生成物濃度昇する。しかし
ながら、残余基質があるにもかかわらず、醗酵生成物濃
度Cpに近付くと、醗酵菌濃度が低下し、m酊生成物濃
度の上昇が止まる。これは、醗酵生成物が所定濃度を越
える、と醗酵筒の代謝明言を生じて増殖を抑制するため
と考えられる。
In Figure 3, the horizontal axis is time, the vertical axis is concentration, curve A is the concentration of fermentation products (e.g. alcohol concentration), curve B is the concentration of fermenting bacteria (e.g. yeast concentration), and curve C is the concentration of residual substrate (e.g. alcohol concentration).
For example, glucose concentration). [The concentration of fermenting bacteria passes through the acclimatization period (tl) after inoculation (t-0), enters the logarithmic growth phase (1+ to t2), and rapidly increases. At the same time substrate I
lt decreases and allll acid product concentration increases. However, even though there is residual substrate, as the fermentation product concentration approaches Cp, the fermentation bacteria concentration decreases and the increase in the m-intoxication product concentration stops. This is thought to be because when the fermentation product exceeds a predetermined concentration, the fermentation tube becomes metabolically active and inhibits proliferation.

以上説明した従来の!1酵装置においては、■馴養用を
要し、醗酵に長時間かがる、■醗酵生成物による代謝聞
書が生じ、生産性(醗酵槽ψ位体積・単位時間当りの生
産! (g/ρ・hr) )の向上を期待できない、■
N菌の混入や予期しない微生物反応の進行等により品質
が低下する等の問題がある。
Conventional as explained above! 1 In a fermentation device, ■ acclimatization is required, fermentation takes a long time, ■ metabolic rate due to fermentation products occurs, and productivity (fermentation tank ψ volume/production per unit time! (g/ρ)・We cannot expect an improvement in hr) ), ■
There are problems such as quality deterioration due to contamination with N bacteria and unexpected progression of microbial reactions.

(発明が解決しようとする問題点) 本発明は、上記問題点を解決するためになされたもので
、馴養用を短縮すると共に、代謝明言を防止して^い生
産性を持続し、更に雑菌の混入を防止し得るriots
装置を提供しようとするものである。
(Problems to be Solved by the Invention) The present invention has been made to solve the above-mentioned problems, and it shortens the acclimation period, prevents metabolic deterioration, maintains high productivity, and further eliminates harmful bacteria. riots that can prevent the contamination of
The aim is to provide equipment.

[発明の構成] (問題点を解決するための手段) 本発明は、隔膜により内部を培1′a室及び原料液室に
区画された膜形反応器と、この反応器の培養液室との間
で醗酵筒を含む培養液の循環がなされる培養槽と、前記
反応器の原料液室との間で原料液の循環がなされる原料
槽と、前記培養槽に無菌水を供給する無菌水槽と、前記
培養槽に連結され、該培養槽中の培養液を分離しIII
酵菌を培養槽に返送すると共に醗酵生成物を生産系に供
給するための濾過器とを具備したことを特徴とする醗酵
装置である。
[Structure of the Invention] (Means for Solving the Problems) The present invention provides a membrane reactor whose interior is divided into a culture medium chamber 1'a and a raw material liquid chamber by a diaphragm, and a culture liquid chamber of this reactor. A culture tank in which a culture solution including a fermentation cylinder is circulated, a raw material tank in which a raw material liquid is circulated between a raw material liquid chamber of the reactor, and a sterile tank that supplies sterile water to the culture tank. a water tank, connected to the culture tank, separating the culture solution in the culture tank;
This fermentation apparatus is characterized by being equipped with a filter for returning the fermentation bacteria to the culture tank and supplying the fermentation product to the production system.

(作用) 上述した本発明の醗酵装置によれば、膜形反応器内では
隔膜を介して醗酵反応が進み、循環する培養液の醗酵生
成物の濃度が上昇するが、培養液を濾過器側に引抜き、
ここで培養液を分離して111!i酵菌を培養槽に返送
すると共にwJ酵生成物を生産系に供給し、かつ培養液
量の減少分を無菌水槽からの無菌水で補充することによ
って、循環する培養系の醗酵生成物濃度の上昇を抑制で
きる。その結果、培養系のII′M生成物濃度を代謝阻
害濃度以下に保ごとができ、生産性を著しく向上できる
(Function) According to the fermentation apparatus of the present invention described above, the fermentation reaction proceeds through the diaphragm in the membrane reactor, and the concentration of fermentation products in the circulating culture solution increases. Pull it out,
Now separate the culture solution and 111! The concentration of fermentation products in the circulating culture system can be increased by returning the i-ferment to the culture tank, supplying the w-J fermentation product to the production system, and replenishing the decreased amount of culture solution with sterile water from the sterile water tank. can suppress the rise in As a result, the II'M product concentration in the culture system can be maintained below the metabolically inhibiting concentration, and productivity can be significantly improved.

また、クローズシステムであるため、雑菌の混入や予期
しない醗酵反応の進行等を防止して高品質の醗酵食品を
再現性よく製造できる。更に、濾過器での培養液の分離
、Wi1m菌の培養槽への返送を行なうことができるた
め、醗酵筒の外部流出を防止できる。
In addition, since it is a closed system, high-quality fermented foods can be produced with good reproducibility by preventing the contamination of various bacteria and the unexpected progression of fermentation reactions. Furthermore, since the culture solution can be separated using a filter and the Wi1m bacteria can be returned to the culture tank, leakage to the outside of the fermentation tube can be prevented.

(発明の実施例) 以下、本発明の実施例を第1図を参照して詳細に説明す
る。
(Embodiments of the Invention) Hereinafter, embodiments of the present invention will be described in detail with reference to FIG.

図中の11は、筒状で上下面が密封された膜形反応器で
あり、この反応器11の内部には培養液室12と原料液
室13とに区画する隔膜14が該反応器11の側面に対
して平行となるように配置されている。この隔膜14は
、例えば分画分子量1oooo〜1000000の限外
濾過膜、ポアサイズ0.01〜1μmの精密濾過膜もし
くはセラミック膜等から形成される。前記膜形反応器1
1の培養液室12の入口には、配管15aを介して培養
液が満たされた培養槽16が連結されており、かつ該配
管15aにはポンプ17aが介装されている。この培養
液は、予めl!!1酊菌(例えば酵母菌)を108〜1
08個/m!2に培養したものである。
Reference numeral 11 in the figure is a cylindrical membrane reactor whose upper and lower surfaces are sealed. Inside the reactor 11, there is a diaphragm 14 that divides the reactor into a culture solution chamber 12 and a raw material solution chamber 13. is arranged parallel to the side surface of the The diaphragm 14 is formed of, for example, an ultrafiltration membrane with a molecular weight cutoff of 1000000 to 1,000,000, a precision filtration membrane with a pore size of 0.01 to 1 μm, or a ceramic membrane. The membrane reactor 1
A culture tank 16 filled with a culture solution is connected to the entrance of the first culture solution chamber 12 via a pipe 15a, and a pump 17a is interposed in the pipe 15a. This culture solution should be prepared in advance. ! 1 intoxicant (e.g. yeast) 108 to 1
08 pieces/m! 2.

前記膜形反応器11の培養液室12の出口には、配管1
5bを介して前記培養槽16に連結されている。こうし
た構成において、前記ポンプ17aを作動させることに
より前記培養槽16中の培養液が配管15a1前記培養
液室12及び配管15bを通って循環する。
At the outlet of the culture solution chamber 12 of the membrane reactor 11, there is a pipe 1.
It is connected to the culture tank 16 via 5b. In such a configuration, by operating the pump 17a, the culture solution in the culture tank 16 is circulated through the pipe 15a1, the culture solution chamber 12, and the pipe 15b.

また、前記反応器11の原料液室13の入口には配管1
5cを介して原料液を収容した原料槽18が連結されて
おり、かつ該配管15cにはポンプ17bが介装されて
いる。前記原料槽18内の原料液は、例えば麹菌、蒸大
豆及び食塩の混合物を低温殺菌した後、無菌水を加えて
流動化して予め麹菌により消化させたものである。前記
反応器11の原料液室13の出口は、配管15dを介し
て生産系を構成する混合器19に連結されている。この
配管15dには、調整弁2oが介装されており、かつ該
調整弁19と前記原料液室13との間の配管156部分
には前記原料槽18と連結する分岐管21が設けられて
いる。こうした構成において、前記調整弁20を閉じた
状態で前記ポンプ17bを作動することによって原料槽
18の原料液が配管15G、原料液室13、配管15d
及び分岐管21を通って循環する。
In addition, a pipe 1 is provided at the entrance of the raw material liquid chamber 13 of the reactor 11.
A raw material tank 18 containing a raw material liquid is connected via a pipe 5c, and a pump 17b is interposed in the pipe 15c. The raw material liquid in the raw material tank 18 is, for example, a mixture of koji mold, steamed soybeans, and salt that is pasteurized, fluidized by adding sterile water, and digested by koji mold in advance. The outlet of the raw material liquid chamber 13 of the reactor 11 is connected to a mixer 19 constituting a production system via a pipe 15d. A regulating valve 2o is interposed in this piping 15d, and a branch pipe 21 connected to the raw material tank 18 is provided in a portion of the piping 156 between the regulating valve 19 and the raw material liquid chamber 13. There is. In such a configuration, by operating the pump 17b with the regulating valve 20 closed, the raw material liquid in the raw material tank 18 is supplied to the pipe 15G, the raw material liquid chamber 13, and the pipe 15d.
and circulates through the branch pipe 21.

更に、前記培養槽16には配管15eを介して無菌水を
収容した無菌水槽22が連結されており、かつ該配管1
5eには前記無菌水槽22の無菌水を前記培養槽16に
供給するためのポンプ17Gが介装されている。なお、
前記培lI槽16には図示しない液面計が挿着されてお
り、該液面計で検知した培養液の水位が設定した水位よ
り下がると。
Furthermore, a sterile water tank 22 containing sterile water is connected to the culture tank 16 via a pipe 15e, and the pipe 1
A pump 17G for supplying sterile water from the sterile water tank 22 to the culture tank 16 is interposed in 5e. In addition,
A liquid level gauge (not shown) is inserted into the culture medium tank 16, and when the water level of the culture liquid detected by the liquid level gauge falls below a set water level.

前記ポンプ17cの作動部に信号が出力され、該ポンプ
17cが作動して無菌水槽22の無菌水が配管15eを
通して培養槽16内に供給できるようになっている。ま
た、前記培養槽16には配管15fを介して濾過器23
が連結されており、かつ該配管15fには前記培養槽1
6内の培養液を前記濾過器23に供給するためのポンプ
17dが介装されている。前記濾過器には、万両分子量
1000〜1oooooの限外濾過膜24が配置されて
いる。
A signal is output to the operating section of the pump 17c, and the pump 17c is activated so that sterile water from the sterile water tank 22 can be supplied into the culture tank 16 through the pipe 15e. In addition, a filter 23 is connected to the culture tank 16 via a pipe 15f.
is connected to the pipe 15f, and the culture tank 1 is connected to the pipe 15f.
A pump 17d for supplying the culture solution in 6 to the filter 23 is interposed. An ultrafiltration membrane 24 having a molecular weight of 1000 to 1000 is disposed in the filter.

前記濾過器23に供給された培養液は、その限外81過
y!24で分離され、分離された一方の醗酵菌は配管1
50を介して前記培養槽16に返送され、他方のII酊
生成物は配管15hを介して前記混合器19に供給され
る。
The culture solution supplied to the filter 23 exceeds its limit of 81 y! 24, and one of the separated fermentation bacteria is transferred to pipe 1.
50 to the culture tank 16, and the other intoxicated product II is supplied to the mixer 19 via pipe 15h.

次に、前述したmM装圏の作用を説明する。Next, the action of the aforementioned mm-enabled sphere will be explained.

まず、例えば麹菌、蒸大豆及び食塩の混合物を低温殺菌
した後、無菌水を加えて流動化して予め麹菌により消化
させた所定量の原料液を原料槽18に導入する。つづい
て、調整弁20を閉じた後、ポンプ17aを作動して培
養槽16内の醗醇菌を含む培養液を配管15a1膜形反
応器11の培養液室12及び配管15bを通して循環さ
せる。
First, for example, a mixture of koji mold, steamed soybeans, and salt is pasteurized, then sterile water is added to fluidize it, and a predetermined amount of the raw material liquid, which has been previously digested by koji mold, is introduced into the raw material tank 18. Subsequently, after closing the regulating valve 20, the pump 17a is operated to circulate the culture solution containing the fermented bacteria in the culture tank 16 through the pipe 15a1, the culture solution chamber 12 of the membrane reactor 11, and the pipe 15b.

この際、培養液の循環流速は醗酵菌の沈降防止及び隔膜
14壁面への醗酵菌の固定化と汚染防止等の観点から1
0〜10’ cR/IRinの範囲、好ましくは102
〜103CIII/1nに設定する。同時にポンプ17
bを作動して原料槽18内の原料液を配管15G、反応
器11の原料液室13、配管15d及び分岐管21を通
して循環させる。この時、前記原料液室13を通って循
環する原料液中の基質が反応器11の隔膜14を通過し
て反対側の培養液室12に濃度拡散し、培養液室12内
を循環する@養液中の醗肝菌により醗酵反応が生じて前
記基質から#Iiam生成物が作られる。
At this time, the circulation flow rate of the culture solution is set at 1 from the viewpoint of preventing sedimentation of the fermenting bacteria, immobilizing the fermenting bacteria on the wall surface of the diaphragm 14, and preventing contamination.
Range of 0-10' cR/IRin, preferably 102
~103CIII/1n. At the same time pump 17
b is operated to circulate the raw material liquid in the raw material tank 18 through the pipe 15G, the raw material liquid chamber 13 of the reactor 11, the pipe 15d, and the branch pipe 21. At this time, the substrate in the raw material liquid circulating through the raw material liquid chamber 13 passes through the diaphragm 14 of the reactor 11, diffuses in concentration to the culture liquid chamber 12 on the opposite side, and circulates within the culture liquid chamber 12. A fermentation reaction occurs by Hepatobacterium in the nutrient solution to produce the #Iiam product from the substrate.

膜形反応器11の培養液室12と培養槽16との間で培
養液を循環させて培養液中に!!1llW生成物を生成
させた後、ポンプ17dを作動して培養槽16内の培養
液を配管15fを通して濾過器23に引抜く。この濾過
器23では、その限外濾過膜24により培養液中の醗酵
菌及び高分子物質と、醗酵生成物及び比較的低分子の物
質とに分離される。醗Wl菌及び高分子物質は、外部に
流出させることなく配管15aを通して前記培養槽16
に返送される。醗酵生成物及び比較的低分子の物質は、
配管15hを通して混合器1つに供給される。この混合
器19には、開閉弁20の解放により原料液が供給され
て、前記醗酵生成物と混合され、所望の醗酵食品が作ら
れる。また、前記培養槽16からの培養液の引抜きに伴
って該培養槽16の水位が下がると、図示しない液面計
からポンプ17cに信号が出力されて該ポンプが作動し
、無菌水槽22内の無菌水が配管15eを通して培養槽
16内に補充され、培養液の循環系の液湧を一定状態に
維持される。
The culture solution is circulated between the culture solution chamber 12 of the membrane reactor 11 and the culture tank 16 to enter the culture solution! ! After producing 111W product, the pump 17d is operated to draw the culture solution in the culture tank 16 to the filter 23 through the pipe 15f. In this filter 23, the ultrafiltration membrane 24 separates the fermentation bacteria and high molecular substances in the culture solution from the fermentation products and relatively low molecular substances. The Wl bacteria and polymer substances are transferred to the culture tank 16 through the piping 15a without leaking to the outside.
will be returned to. Fermentation products and relatively low molecular weight substances are
It is supplied to one mixer through a pipe 15h. The raw material liquid is supplied to the mixer 19 by opening the on-off valve 20 and mixed with the fermentation product to produce a desired fermented food. Further, when the water level of the culture tank 16 decreases as the culture solution is withdrawn from the culture tank 16, a signal is output from the liquid level gauge (not shown) to the pump 17c, which activates the pump. Sterile water is replenished into the culture tank 16 through the pipe 15e, and the flow of the culture solution circulation system is maintained at a constant state.

上述した膜形反応器11の原料液室13と原料槽18と
の間での原料液の循環、及び膜形反応器11の培養液液
室12と培養槽16との間での培養液の循環においては
、下記(1)式に示すように隔膜14を透過する基質に
対応したl[1酊生成物が発生する。また、培養槽16
からの培養液の濾過器23への引抜きにより、培養循環
系のWIJ酊生酸生成物失量は下記(2式で表わされる
Circulation of the raw material liquid between the raw material liquid chamber 13 and the raw material tank 18 of the membrane reactor 11 mentioned above, and circulation of the culture liquid between the culture liquid chamber 12 of the membrane reactor 11 and the culture tank 16. During the circulation, a l[1 intoxication product corresponding to the substrate passing through the diaphragm 14 is generated as shown in equation (1) below. In addition, the culture tank 16
By drawing the culture fluid from the culture medium into the filter 23, the loss of WIJ acid product in the culture circulation system is expressed by the following equation (2).

醗酵生成物の発生!=Jd−8−k  ・・・(1)m
酵生成物の流失量=Cr −Qp   ・・・(2但し
、上2(1)、(2)の式中において、Jd:隔111
14を介して濃度拡散する基質フラックスC9/cd−
sea)、 S:隔1114の表面積(cd )、 に:定数、 CF:培養液の醗酵生成物濃度〔g/c#+3〕、Qp
:!II過器23の透過液流fjk Crys3/se
a )である。
Generation of fermentation products! =Jd-8-k...(1)m
Amount of fermentation product runoff = Cr - Qp (2 However, in the formulas of above 2 (1) and (2), Jd: interval 111
Substrate flux C9/cd− that concentration diffuses through 14
sea), S: surface area of septum 1114 (cd), N: constant, CF: fermentation product concentration of culture solution [g/c#+3], Qp
:! Permeate flow fjk Crys3/se of II filter 23
a).

定常状態では、培養液の循環系内の醗酵生成物の発生■
と流失量とは等しい。従って、醗酵生成物濃度(CF 
)は下記(3)式で表わされる。即ち、濾過器23の透
過液流量(Q、)の操作により醗酵生成物濃度(CF 
)の制御が可能であり、これによって培養液の循環系の
醗酵生成物濃度を代謝阻害濃度以下に維持することがで
き、生産性を著しく向上できる。
At steady state, the generation of fermentation products within the circulatory system of the culture medium■
and the amount lost are equal. Therefore, the fermentation product concentration (CF
) is expressed by the following formula (3). That is, by controlling the permeate flow rate (Q) of the filter 23, the fermentation product concentration (CF
), thereby making it possible to maintain the concentration of fermentation products in the circulation system of the culture solution below the metabolically inhibiting concentration, thereby significantly improving productivity.

CF−(Jd −8−k)/QP ・・・(3)また、
培養液の循環系において醗酵生成物の一部は膜形反応器
11の隔l!14を通して原料液室13に濃度拡散し、
原料液の循環系に移行して混合された後、開閉弁20を
通して混合器19に供給される。このため、原料液循環
系においても下記(4)式に示す原料液の醗酵生成物の
濃度(CM)のバランスが生じる。
CF-(Jd-8-k)/QP...(3) Also,
In the circulation system of the culture solution, a part of the fermentation product is transferred to the membrane reactor 11. The concentration is diffused into the raw material liquid chamber 13 through 14,
After being transferred to the raw material liquid circulation system and mixed, it is supplied to the mixer 19 through the on-off valve 20. Therefore, in the raw material liquid circulation system as well, the concentration (CM) of the fermentation product of the raw material liquid is balanced as shown by the following equation (4).

CM−(Jd −8−k)/QP  ・・・(4)以上
説明した本実施例によれば、次の列挙する種々の効果を
発揮できる。
CM-(Jd-8-k)/QP (4) According to this embodiment described above, various effects listed below can be achieved.

■醗酵菌が生成する#1酵生成物の濃度を制御できる。■The concentration of #1 fermentation product produced by fermentation bacteria can be controlled.

■S酵菌の流出を濾過器23により防止できる。(2) Outflow of S yeast can be prevented by the filter 23.

■前記■により培養液中の醗酵菌濃度の管埋が容易とな
る。
(2) The above (2) makes it easy to determine the concentration of fermenting bacteria in the culture solution.

■前記■及び■により連続的なS酵が可能となると共に
醗酵生成物濃度を代謝阻害濃度以下に維持でき、醗酵生
成物の生産性、ひいてはWJW1食品の生産性を向上で
きる。
(2) The above (2) and (2) enable continuous S fermentation and maintain the fermentation product concentration below the metabolic inhibition concentration, thereby improving the productivity of the fermentation product and, by extension, the productivity of the WJW1 food.

■無菌状態でかつクローズシステムであるため、雑菌の
混入や予期しない醗酵反応の進行等を防止でき、高品質
の醗酵食品を得ることができる。
■As it is a sterile and closed system, it is possible to prevent the contamination of various bacteria and the unexpected progression of fermentation reactions, making it possible to obtain high-quality fermented foods.

■原料液を循環するため、撹拌機が不要となる。■Since the raw material liquid is circulated, a stirrer is not required.

[発明の効果] 以上詳述した如く、本発明によれば馴養期を短縮すると
共に、代謝阻害を防止して高い生産性を持続し、更に雑
菌の混入を防止し得るl1g酵装置を提供できる。
[Effects of the Invention] As detailed above, according to the present invention, it is possible to provide an 11g fermentation apparatus that can shorten the acclimatization period, prevent metabolic inhibition, maintain high productivity, and prevent contamination with various bacteria. .

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明の実施例における醗酵装置を示す概略図
、第2図は従来の醗酵装置を示す概略図、第3図は醗酵
反応のバッチ実験における特性図である。 11・・・膜形反応器、12・・・培養液室、13・・
・原料液室、14・・・隔膜、16・・・培養液L17
a〜17d・・・ポンプ、18・・・原料槽、19・・
・混合器、20・・・調整弁、22・・・無菌水槽、2
3・・・濾過器。
FIG. 1 is a schematic diagram showing a fermentation apparatus in an embodiment of the present invention, FIG. 2 is a schematic diagram showing a conventional fermentation apparatus, and FIG. 3 is a characteristic diagram in a batch experiment of fermentation reaction. 11... Membrane reactor, 12... Culture solution chamber, 13...
- Raw material liquid chamber, 14...diaphragm, 16...culture solution L17
a to 17d...pump, 18...raw material tank, 19...
・Mixer, 20... Regulating valve, 22... Sterile water tank, 2
3...filter.

Claims (1)

【特許請求の範囲】[Claims] 隔膜により内部を培養液室及び原料液室に区画された膜
形反応器と、この反応器の培養液室との間で醗酵菌を含
む培養液の循環がなされる培養槽と、前記反応器の原料
液室との間で原料液の循環がなされる原料槽と、前記培
養槽に無菌水を供給する無菌水槽と、前記培養槽に連結
され、該培養槽中の培養液を分離し醗酵菌を培養槽に返
送すると共に醗酵生成物を生産系に供給するための濾過
器とを具備したことを特徴とする醗酵装置。
A membrane reactor whose interior is divided into a culture solution chamber and a raw material solution chamber by a diaphragm, a culture tank in which a culture solution containing fermentation bacteria is circulated between the culture solution chamber of this reactor, and the reactor. a raw material tank in which raw material liquid is circulated between the raw material liquid chamber, a sterile water tank that supplies sterile water to the culture tank, and a sterile water tank that is connected to the culture tank and separates the culture liquid in the culture tank for fermentation. A fermentation device characterized by comprising a filter for returning bacteria to a culture tank and supplying a fermentation product to a production system.
JP61103415A 1986-05-06 1986-05-06 Fermentation apparatus Pending JPS62259576A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61103415A JPS62259576A (en) 1986-05-06 1986-05-06 Fermentation apparatus

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61103415A JPS62259576A (en) 1986-05-06 1986-05-06 Fermentation apparatus

Publications (1)

Publication Number Publication Date
JPS62259576A true JPS62259576A (en) 1987-11-11

Family

ID=14353413

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61103415A Pending JPS62259576A (en) 1986-05-06 1986-05-06 Fermentation apparatus

Country Status (1)

Country Link
JP (1) JPS62259576A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0242992A (en) * 1988-08-03 1990-02-13 Tanabe Seiyaku Co Ltd Reaction using biocatalyst and device for said reaction

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0242992A (en) * 1988-08-03 1990-02-13 Tanabe Seiyaku Co Ltd Reaction using biocatalyst and device for said reaction

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