JPH0715440Y2 - Reaction vessel - Google Patents

Reaction vessel

Info

Publication number
JPH0715440Y2
JPH0715440Y2 JP1989110417U JP11041789U JPH0715440Y2 JP H0715440 Y2 JPH0715440 Y2 JP H0715440Y2 JP 1989110417 U JP1989110417 U JP 1989110417U JP 11041789 U JP11041789 U JP 11041789U JP H0715440 Y2 JPH0715440 Y2 JP H0715440Y2
Authority
JP
Japan
Prior art keywords
container
sensor
nozzle
incubator
gas
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 - Lifetime
Application number
JP1989110417U
Other languages
Japanese (ja)
Other versions
JPH0350900U (en
Inventor
充 片倉
幹夫 角田
孝良 木村
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.)
Tsumura and Co
Original Assignee
Tsumura and Co
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 Tsumura and Co filed Critical Tsumura and Co
Priority to JP1989110417U priority Critical patent/JPH0715440Y2/en
Publication of JPH0350900U publication Critical patent/JPH0350900U/ja
Application granted granted Critical
Publication of JPH0715440Y2 publication Critical patent/JPH0715440Y2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12MAPPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
    • C12M27/00Means for mixing, agitating or circulating fluids in the vessel
    • C12M27/02Stirrer or mobile mixing elements

Landscapes

  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Zoology (AREA)
  • Biomedical Technology (AREA)
  • Sustainable Development (AREA)
  • Microbiology (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Biotechnology (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)

Description

【考案の詳細な説明】 [産業上の利用分野] 本考案は反応容器に係り、特に容器内面壁への付着物の
生成を解決する反応容器に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial field of use] The present invention relates to a reaction vessel, and more particularly to a reaction vessel for solving the formation of deposits on the inner wall of the vessel.

[従来の技術] 各種研究の検体としての動・植物細胞又は微生物は、一
般に栄養としての空気を導入するエアノズルや攪拌器を
備えた培養器中にて培養される。このような培養器の容
器内に保持される培養液の液位近傍の容器内面壁には、
動・植物細胞又は微生物等からなる固形物が付着し、こ
の付着層は経時的に成長してゆく。そして、この付着層
中の動・植物細胞又は微生物は培養条件が満足されない
状況におかれることから、死滅に到る。このような死滅
細胞の発生は培養液中の動・植物細胞又は微生物数を減
らす直接的な原因となる上に、培養液中の動・植物細胞
又は微生物の増殖に対して悪影響を及ぼし、培養液中の
動・植物細胞又は微生物を死滅させる恐れもある。ま
た、一度付着するとその部分で細胞が生育するものも含
めて付着量が急激に増加し、激しい場合には培養表面か
ら上部にわたって、大きな細胞のかたまりを形成してし
まう。従ってこれを可及的速やかに取り除く、即ち、微
生物培養液中に戻す必要がある。
[Prior Art] Animal / plant cells or microorganisms as specimens for various studies are generally cultivated in an incubator equipped with an air nozzle or an agitator for introducing air as nutrients. On the inner wall of the container near the liquid level of the culture solution held in the container of such an incubator,
Solids composed of animal / plant cells or microorganisms adhere, and the adhered layer grows with time. The animal / plant cells or microorganisms in the adhesion layer are killed because the culture conditions are not satisfied. The generation of such dead cells has a direct cause of reducing the number of animal / plant cells or microorganisms in the culture solution, and also has an adverse effect on the growth of the animal / plant cells or microorganisms in the culture solution. There is also a risk of killing animal / plant cells or microorganisms in the liquid. In addition, once attached, the amount of attached cells, including those in which cells grow at that portion, increases rapidly, and when they are violent, large cell clusters are formed from the culture surface to the upper portion. Therefore, it is necessary to remove this as soon as possible, that is, to return it to the microbial culture solution.

また、培養器に限らず、各種分散液や溶液等を保持する
反応容器では、容器内面壁の液位近傍に分散質や溶質が
付着し、これが液濃度や液組成を変える原因となるな
ど、付着物による問題が生じることから、これを速やか
に液中に戻す必要がある場合がある。
Further, not limited to the incubator, in a reaction container for holding various dispersions or solutions, the dispersoid or solute adheres to the vicinity of the liquid level on the inner wall of the container, which causes the change in liquid concentration or liquid composition, etc. Since there is a problem due to deposits, it may be necessary to quickly return this to the liquid.

[考案が解決しようとする課題] 従来、培養器の容器内面壁の付着層の除去については、
特に対策は講じられておらず、作業員が付着層を目視に
て確認した際に磁石などを用いて、かき取るか、槽全体
を揺すり落とすなどの処理がなされていた。また、他の
反応容器についても同様である。しかしながら、このよ
うな人為的な処理では作業効率が悪く、人手を要する上
に付着層を常に速やかに除去することができず、付着層
による問題の解決策をして十分なものとは言えない。
[Problems to be Solved by the Invention] Conventionally, regarding removal of the adhesion layer on the inner wall of the container of the incubator,
No particular measures were taken, and when the operator visually confirmed the adhesion layer, a treatment such as scraping or shaking off the entire tank was performed using a magnet or the like. The same applies to other reaction vessels. However, such an artificial treatment is inefficient in working efficiency, requires labor and cannot always remove the adhering layer quickly, and it cannot be said that a solution to the problem due to the adhering layer is sufficient. .

なお、培養器内の液を常時バブリングしておくことによ
り、付着層の生成を防止することも考えられるが、この
場合には培養液が泡立ち、良好な培養が行なえない。ま
た、バブリングのための動力コストが高くつくため好ま
しくない。
It is possible to prevent the formation of an adherent layer by constantly bubbling the liquid in the incubator, but in this case, the culture liquid foams and good culture cannot be performed. Moreover, the power cost for bubbling is high, which is not preferable.

本考案は、上記従来の問題点を解決し、付着層を自動的
かつ効率的に除去することができる反応容器を提供する
ことを目的とする。
It is an object of the present invention to solve the above-mentioned conventional problems and to provide a reaction container capable of automatically and efficiently removing the adhesion layer.

[課題を解決するための手段] 本考案の反応容器は、液を保持する透明な容器と、該容
器内の液面位よりも下方に気体放出口を有するガラノズ
ルと、該ガスノズルに気体を供給する気体供給手段と、
前記容器の内面壁のうち液面位付近の付着物を検出する
ためのセンサであって、該容器の外側に配置された光学
式センサと、該センサの信号に基づいて前記気体供給手
段を作動させる制御器とを有することを特徴とする。
[Means for Solving the Problems] A reaction container of the present invention is a transparent container for holding a liquid, a glass nozzle having a gas discharge port below the liquid level in the container, and a gas supply to the gas nozzle. Gas supply means for
A sensor for detecting deposits near the liquid level on the inner wall of the container, which is an optical sensor arranged outside the container, and operates the gas supply means based on a signal from the sensor. And a controller for controlling the control.

[作用] 本考案の反応容器では、液を保持する容器の内面壁の液
面位付近に付着物が生成した場合には、センサで検出さ
れる。そして、センサの検出信号に基づいて気体供給手
段が作動される。気体供給手段からの気体は、ノズルの
容器内の液面位よりも下方に設けられた気体放出口から
放出され、放出れた気体により液がバブリングされる。
これにより容器内面壁の付着物は効率的に洗い落される
如くして除去される。
[Operation] In the reaction container of the present invention, when a deposit is formed near the liquid level on the inner wall of the container holding the liquid, the sensor detects it. Then, the gas supply means is operated based on the detection signal of the sensor. The gas from the gas supply means is discharged from the gas discharge port provided below the liquid level in the container of the nozzle, and the discharged gas causes the liquid to bubble.
As a result, the deposits on the inner wall of the container are efficiently washed off and removed.

このように必要時にのみバブリングを行なうため、バブ
リングに要する動力コストは低廉である。
Since the bubbling is performed only when necessary, the power cost required for the bubbling is low.

従って、本考案の反応容器によれば、容器内面壁の付着
物を、人手を要することなく、自動的にかつ効率的に確
実にしかも低コストにて除去することが可能とされる。
Therefore, according to the reaction container of the present invention, it is possible to remove the deposits on the inner wall of the container automatically, efficiently, reliably and at low cost, without requiring any manpower.

しかも、付着物の検出に用いるセンサは、容器外側に配
置された光学式センサであるため、液のバブリング時に
センサが液で汚れたり、センサ自体が付着物で汚染され
たりすることがなく、誤検出のおそれがないため、付着
物を確実に検出することができる。また、センサの故障
の問題もない。
Moreover, since the sensor used to detect the adhered matter is an optical sensor located outside the container, the sensor is not contaminated with the liquid when bubbling the liquid, and the sensor itself is not contaminated with the adhered matter. Since there is no possibility of detection, it is possible to reliably detect the attached matter. Also, there is no problem of sensor failure.

[実施例] 以下に図面を参照して本考案の実施例について説明す
る。
[Embodiment] An embodiment of the present invention will be described below with reference to the drawings.

第1図,第2図は各々本発明の反応容器の一実施例に係
る培養器を示す断面図であり、同一機能を有する部材に
は同一符号を付してある。
1 and 2 are cross-sectional views showing an incubator according to an embodiment of the reaction container of the present invention, in which members having the same function are designated by the same reference numerals.

第1図の培養器1Aは、培養液2を保持する透明な容器
と、該容器3内の液面位2Aよりも下方に空気放出口4aを
有するノズル4と、該ノズル4に空気を供給する空気供
給管5及びエアコンプレッサ6と、前記容器3の内面壁
のうち液面位2A付近の付着物を検出するセンサ7Aと、該
センサ7Aの信号に基いてエアコンプレッサ6を作動させ
る制御器8とを有する。センサ7Aは、発した光の反射
率、屈折率等を測定し、その変化により付着物を検出す
る光学式センサであり、容器3の外側の液面位2A近傍に
設けられている。図中、9は攪拌器、10は培養空気導入
管、11は容器3の蓋である。
The incubator 1A shown in FIG. 1 has a transparent container for holding the culture solution 2, a nozzle 4 having an air discharge port 4a below the liquid level 2A in the container 3, and an air supply to the nozzle 4. Air supply pipe 5 and air compressor 6, a sensor 7A for detecting deposits on the inner wall of the container 3 near the liquid level 2A, and a controller for operating the air compressor 6 based on the signal from the sensor 7A. 8 and. The sensor 7A is an optical sensor that measures the reflectance, the refractive index, and the like of the emitted light and detects adhering substances based on changes in the reflectance, and is provided outside the container 3 near the liquid level 2A. In the figure, 9 is a stirrer, 10 is a culture air introduction tube, and 11 is a lid of the container 3.

本実施例の培養器1Aにおいては、容器3の内面壁に付着
物が付着すると、これをセンサ7Aが検知して付着物検出
信号を制御器8に送る。制御器8は、入力された付着物
検出信号に基いてエアコンプレッサ6を作動させて、空
気供給管5、ノズル4を経て空気を供給する。ノズル4
の放出口4aより放出された空気は、培養液2をバブリン
グさせる。これにより付着物は洗い落される如くして剥
離される。
In the incubator 1A of the present embodiment, when an adhering matter adheres to the inner wall of the container 3, the sensor 7A detects the adhering matter and sends an adhering matter detection signal to the controller 8. The controller 8 operates the air compressor 6 based on the input adhering matter detection signal to supply air through the air supply pipe 5 and the nozzle 4. Nozzle 4
The air discharged from the discharge port 4a of bubbling causes the culture solution 2 to bubble. As a result, the deposits are peeled off as if they were washed off.

なお、本実施例において、ノズル4は環状のノズル本体
4Aから3〜6本のノズル先端部4Bが立設されたものであ
って、このノズル先端部4Bは、容器3の内面壁の付着物
を満遍なく剥離することができるように、円周方向に等
分位置に設けられている。
In this embodiment, the nozzle 4 is an annular nozzle body.
3 to 6 nozzle tip portions 4B are erected from 4A, and these nozzle tip portions 4B are arranged in the circumferential direction so that the adhered matter on the inner wall of the container 3 can be evenly peeled off. It is provided in equal positions.

第2図に示す培養器1Bは、エアノズル14を容器3の下方
の側面から挿入して設けたことが第1図に示すものと異
なる。即ち、第2図に示す培養器1Bは、容器3の下方側
面部に蓋3A付きのノズル挿入口3Bが設けれており、この
挿入口3Bにエアコンプレッサ6からの空気を空気供給管
15を経て供給するエアノズル14が挿入されている。
The incubator 1B shown in FIG. 2 differs from that shown in FIG. 1 in that the air nozzle 14 is provided by inserting it from the lower side surface of the container 3. That is, in the incubator 1B shown in FIG. 2, a nozzle insertion port 3B with a lid 3A is provided on the lower side surface portion of the container 3, and air from the air compressor 6 is supplied to this insertion port 3B by an air supply pipe.
An air nozzle 14 supplied via 15 is inserted.

この培養器1Bにおいても、センサ7Aで付着物を検出する
とその信号を制御器8に送り、制御器8では入力された
信号に基づいて、エアコンプレッサ6を作動させて培養
液2をバブリングさせることにより付着物を剥離させ
る。
Also in this incubator 1B, when the sensor 7A detects an adhering substance, the signal is sent to the controller 8, and the controller 8 operates the air compressor 6 to bubble the culture solution 2 based on the input signal. The attached matter is peeled off by.

なお、本実施例においても、エアノズル14は容器3の内
面壁の付着物を満遍なく剥離することができるように、
3〜6本を均等位置に設けるようにするのが好ましい。
Note that, also in this embodiment, the air nozzle 14 is capable of uniformly removing the deposits on the inner wall of the container 3,
It is preferable to provide 3 to 6 at even positions.

因みに、第1図,第2図に示すような本考案の培養器を
用いて植物細胞培養実験を行なったところ、従来におい
ては、1〜7日程度で付着層が生成していたのに対し
て、センサの検出により自動的に0.5〜24時間毎にバブ
リングが実施され、付着層の形成、成長は全くおこらな
かった。例えば、植物細胞を10l培養器にて、生重量500
〜1000g保持した場合、1日で細胞付着が生じたが、本
考案によれば2〜3時間間隔でバブリングが実施され、
付着はおこらなかった。
By the way, when a plant cell culture experiment was carried out using the incubator of the present invention as shown in FIGS. 1 and 2, in the conventional case, the adherent layer was formed in about 1 to 7 days. Then, bubbling was automatically performed every 0.5 to 24 hours by the detection of the sensor, and the formation and growth of the adhesion layer did not occur at all. For example, plant cells are placed in a 10-liter incubator and the fresh weight is 500
When ~ 1000g was retained, cell adhesion occurred in one day, but according to the present invention, bubbling was performed at intervals of 2-3 hours,
No adhesion occurred.

本考案においては、センサによる付着物検出に周期性を
見出した際には、センサを用いず、一定時間毎にコンプ
レッサを作動させるようにして機能させることもでき
る。また、一定時間毎にコンプレッサを作動させると共
に、センサにより付着物が検出された時にもコンプレッ
サを作動させるようにして機能させることもできる。
In the present invention, when the periodicity is detected in the detection of the adhered substances by the sensor, the sensor can be used and the compressor can be operated at regular intervals. It is also possible to operate the compressor at regular time intervals and also to operate the compressor when an adhering substance is detected by the sensor.

なお、以上の説明では本考案の反応容器を植物細胞培養
器に適用した例について説明したが、本考案は培養器に
限らず、他のあらゆる反応容器に適用できることは言う
までもない。また、供給する気体は空気に限らず、非酸
化ガスが好ましい反応容器であれば窒素等の他の気体を
用いることができる。
In the above description, an example in which the reaction container of the present invention is applied to a plant cell incubator has been described, but it goes without saying that the present invention is not limited to an incubator and can be applied to any other reaction container. Further, the gas to be supplied is not limited to air, and other gases such as nitrogen can be used as long as the reaction container is preferably a non-oxidizing gas.

さらに、本考案の反応容器を適用した培養器において
は、植物細胞、動物細胞のみならず、あらゆる微生物を
培養することができ、特に、培養に際して培養液位近傍
の培養器内面壁に付着しやすい、カルス細胞、大腸菌、
酵母菌等の細胞の培養に有効である。
Furthermore, in the incubator to which the reaction container of the present invention is applied, not only plant cells and animal cells but also all kinds of microorganisms can be cultivated. , Callus cells, E. coli,
It is effective for culturing cells such as yeast.

[考案の効果] 以上詳述した通り、本考案の反応容器によれば、容器内
面壁の付着物を、人手を要することなく、自動的にかつ
効率的に確実にしかも低コストにて除去することが可能
とされる。従って、本考案の反応容器を用いることによ
り、例えば、動・植物細胞又は微生物培養においては、
死滅細胞の生成を防止して高効率培養が可能とされ、ま
た、分散液や溶液の保持容器として、高精度な濃度ない
し組成管理が可能とされる。
[Advantages of the Invention] As described in detail above, according to the reaction container of the present invention, the deposits on the inner wall of the container can be removed automatically, efficiently, reliably, and at low cost without requiring manpower. Is possible. Therefore, by using the reaction container of the present invention, for example, in animal / plant cell or microbial culture,
The production of dead cells can be prevented, high-efficiency culture can be performed, and highly accurate concentration or composition control can be performed as a container for holding a dispersion liquid or a solution.

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

第1図及び第2図は各々本考案の反応容器の一実施例を
示す断面図である。 1A、1B…微生物培養器、1…微生物培養液、3…容器、
4…ノズル、6エアコンプレッサ、7A…センサ、8…制
御器。
1 and 2 are sectional views showing an embodiment of the reaction container of the present invention. 1A, 1B ... Microorganism incubator, 1 ... Microorganism culture solution, 3 ... Container,
4 ... Nozzle, 6 air compressor, 7A ... Sensor, 8 ... Controller.

Claims (1)

【実用新案登録請求の範囲】[Scope of utility model registration request] 【請求項1】液を保持する透明な容器と、該容器内の液
面位よりも下方に気体放出口を有するガスノズルと、該
ガスノズルに気体を供給する気体供給手段と、前記容器
の内面壁のうち液面位付近の付着物を検出するためのセ
ンサであって、該容器の外側に配置された光学式センサ
と、該センサの信号に基づいて前記気体供給手段を作動
させる制御器とを有することを特徴とする反応容器。
1. A transparent container for holding a liquid, a gas nozzle having a gas discharge port below the liquid level in the container, gas supply means for supplying gas to the gas nozzle, and an inner wall of the container. A sensor for detecting deposits in the vicinity of the liquid level, an optical sensor arranged outside the container, and a controller for operating the gas supply means based on a signal from the sensor. A reaction container having.
JP1989110417U 1989-09-21 1989-09-21 Reaction vessel Expired - Lifetime JPH0715440Y2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1989110417U JPH0715440Y2 (en) 1989-09-21 1989-09-21 Reaction vessel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1989110417U JPH0715440Y2 (en) 1989-09-21 1989-09-21 Reaction vessel

Publications (2)

Publication Number Publication Date
JPH0350900U JPH0350900U (en) 1991-05-17
JPH0715440Y2 true JPH0715440Y2 (en) 1995-04-12

Family

ID=31658947

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1989110417U Expired - Lifetime JPH0715440Y2 (en) 1989-09-21 1989-09-21 Reaction vessel

Country Status (1)

Country Link
JP (1) JPH0715440Y2 (en)

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