JPH0838156A - Culture of alga and apparatus therefor - Google Patents
Culture of alga and apparatus thereforInfo
- Publication number
- JPH0838156A JPH0838156A JP20790794A JP20790794A JPH0838156A JP H0838156 A JPH0838156 A JP H0838156A JP 20790794 A JP20790794 A JP 20790794A JP 20790794 A JP20790794 A JP 20790794A JP H0838156 A JPH0838156 A JP H0838156A
- Authority
- JP
- Japan
- Prior art keywords
- culture
- stage
- algae
- tube
- pipe
- 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.)
- Withdrawn
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS 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
- C12M23/00—Constructional details, e.g. recesses, hinges
- C12M23/22—Transparent or translucent parts
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS 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
- C12M21/00—Bioreactors or fermenters specially adapted for specific uses
- C12M21/02—Photobioreactors
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS 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
- C12M23/00—Constructional details, e.g. recesses, hinges
- C12M23/02—Form or structure of the vessel
- C12M23/06—Tubular
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS 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
- C12M23/00—Constructional details, e.g. recesses, hinges
- C12M23/34—Internal compartments or partitions
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS 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
- C12M23/00—Constructional details, e.g. recesses, hinges
- C12M23/48—Holding appliances; Racks; Supports
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS 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
- C12M29/00—Means for introduction, extraction or recirculation of materials, e.g. pumps
- C12M29/06—Nozzles; Sprayers; Spargers; Diffusers
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS 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
- C12M31/00—Means for providing, directing, scattering or concentrating light
- C12M31/10—Means for providing, directing, scattering or concentrating light by light emitting elements located inside the reactor, e.g. LED or OLED
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical & Material Sciences (AREA)
- Zoology (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Sustainable Development (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Clinical Laboratory Science (AREA)
- Molecular Biology (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、魚介類の種苗生産等に
利用されるクロレラ等の単細胞藻類を、短期間に高密度
でかつ安価に大量生産するための培養装置およびその方
法に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a culturing apparatus and a method for mass-producing unicellular algae such as chlorella, which are used for seedling production of fish and shellfish, in a short period of time at high density and at low cost. is there.
【0002】[0002]
【従来の技術】魚介類の種苗生産などで使用されるクロ
レラ等の単細胞藻類は、方形・円形の培養水槽(容量1
〜200トン)にエアレーションホースをいれ、このホ
ースから放出される空気で、藻類の培養液を撹拌させな
がら開放系で培養されている。そして、クロレラ等の培
養密度が種苗生産に使用できる細胞数迄増殖した段階で
その一部を使用し、その使用量に相当する新しい培養液
を追加して、薄まった細胞数がさらに増殖して元の細胞
数に復するのを待って再び使用するという方法で培養、
実用に供されている。また、特開平3−266973で
提案されているクロレラ等の培養装置は、密閉培養槽で
純粋培養条件を保持し、自走式撹拌機で水槽内を洗浄撹
拌しながら連続培養するもので、当業者がこの装置を採
用するには既存設備の更新が必要となり多大の経費を要
するため実用には供されておらず、前述の方法が一般的
に利用されている。2. Description of the Related Art Single cell algae such as chlorella used in the production of seeds and seedlings of fish and shellfish are cultivated in a rectangular or circular culture tank (capacity 1
(About 200 tons), an aeration hose is put in, and the air discharged from this hose is cultivated in an open system while stirring the culture solution of algae. Then, when the culture density of Chlorella etc. has grown to the number of cells that can be used for seedling production, a part of it is used and a new culture solution corresponding to the amount used is added, and the number of diluted cells further grows. Culture by waiting for the cell number to return to its original value and then using it again,
It is put to practical use. Further, the culturing apparatus such as Chlorella proposed in Japanese Patent Laid-Open No. 3-266973 holds pure culture conditions in a closed culture tank and continuously cultures while washing and stirring the inside of the water tank with a self-propelled stirrer. In order for a trader to adopt this device, the existing equipment needs to be renewed and it requires a large amount of money, so it has not been put into practical use, and the above-mentioned method is generally used.
【0003】[0003]
【発明が解決しようとする課題】上述した従来の培養方
法は、開放系で培養されているために培養不調となる様
々な危険と隣り合わせていて、一度、培養不調となった
ときには、保存種から培養のやり直しをしているが元の
状態に短期間で回復させることは困難である。このた
め、多くの種苗生産業者はそれぞれが開放系で大量培養
しているものを、培養不調となった種苗生産業者に大量
培養用の種として融通し合っているのが現実であり、防
疫という観点からは好ましいものではない。本発明は、
上記のような欠点を除去したもので当業者の既存設備を
利用し、クロレラ藻類等の培養を安定的かつ計画的に生
産することを目的とする。The above-mentioned conventional culturing method is adjacent to various dangers of culture failure because it is cultivated in an open system. Although culturing is repeated, it is difficult to restore the original state in a short period of time. For this reason, many seedling producers are actually cultivating large-scale cultures in an open system, and they are used as seeds for mass-culturing by seedling producers who are in poor culture. It is not preferable from the viewpoint. The present invention
It is intended to stably and systematically produce a culture of chlorella algae or the like by utilizing the existing equipment of those skilled in the art without removing the above-mentioned drawbacks.
【0004】[0004]
【課題を解決するための手段】上記課題を解決するため
に、本発明の第1発明の藻類の培養装置は、台座の中央
部分に透明管を立設し、この透明管の上端に空気室を構
成すると共に内部には複数の光源を配置し、さらに前記
空気室の上端には光透過性の培養容器を吊り下げるため
のフックを備えた上板を固定し、上記培養容器の内部に
は上記空気室と連通したチューブを挿入してなることを
特徴とし、第2発明の藻類の培養装置は、傾斜スタンド
の上端に光透過性の培養容器の上端を固定して傾斜板上
に載置し、傾斜スタンドの上端に設けたエアー管に連通
するチューブを培養容器内に挿入してなることを特徴と
し、第3発明の藻類の培養装置は、水槽の中心部にアン
ドンを固定し、このアンドン内部に水中ポンプを設置
し、水中ポンプから培養液圧送用のパイプを延出せし
め、このパイプの先端を水槽の内側下方に開放せしめ、
この先端から水槽内の培養液を噴出させる一方、上記パ
イプを分岐して水槽の外部と連通せしめたことを特徴と
し、第4発明の藻類の培養装置は、台座の中央部分に透
明管を立設し、この透明管の上端に空気室を構成すると
共に内部には複数の光源を配置し、さらに前記空気室の
上端には光透過性の培養容器を吊り下げるためのフック
を備えた上板を固定し、上記培養容器の内部には上記空
気室と連通したチューブを挿入してなる第一段階の培養
装置と、傾斜スタンドの上端に光透過性の培養容器の上
端を固定して傾斜板上に載置し、傾斜スタンドの上端に
設けたエアー管に連通するチューブを培養容器内に挿入
してなる第二段階の培養装置と、水槽の中心部にアンド
ンを固定し、このアンドン内部に水中ポンプを設置し、
水中ポンプから培養液圧送用のパイプを延出せしめ、こ
のパイプの先端を水槽の内側下方に開放せしめ、この先
端から水槽内の培養液を噴出させる一方、上記パイプを
分岐して水槽の外部と連通せしめてなる第三段階の培養
装置からなることを特徴とし、第5発明の藻類の培養方
法は、光源の周囲に配置した光透過性の培養容器により
藻類を培養し、その後この藻類の一部をその種として利
用し、かつその大部分を第二段階の種として利用するこ
とにより藻類の培養液量を増加させ、純粋培養による種
の保存と第二段階の培養過程への種の供給を行う第一段
階と、光透過性の培養容器を傾斜スタンドに設置して、
準閉鎖系培養方法により第一段階で得られた藻類を純粋
培養し、第三段階の開放系大量培養過程へその全量を種
として供給する第二段階と、藻類培養の水槽に水中ポン
プと水流発生装置を設備して第二段階で得られた培養液
を回転・攪拌させながら開放系のままで大量培養し、そ
の後全量を収穫する第三段階からなり、上記第一、第
二、第三の各段階を連続して行うことを特徴とする。In order to solve the above problems, in the algae culture device of the first invention of the present invention, a transparent tube is erected at the center of the pedestal, and an air chamber is provided at the upper end of the transparent tube. And a plurality of light sources are arranged inside, and an upper plate having a hook for suspending a light-transmissive culture container is fixed to the upper end of the air chamber, and the inside of the culture container is The algae culture device of the second invention is characterized in that a tube communicating with the air chamber is inserted, and the upper end of the light-transmissive culture container is fixed to the upper end of the tilt stand and placed on the tilt plate. Then, a tube communicating with an air tube provided at the upper end of the tilt stand is inserted into the culture container, and the algae culture device of the third invention fixes Andon at the center of the aquarium. Install submersible pump inside Andong Nutrient solution pipe allowed extending the for pumping, allowed open distal end of the pipe to the inside below the water tank,
While the culture solution in the water tank is jetted from this tip, the pipe is branched so as to communicate with the outside of the water tank, and the algae culture device of the fourth invention has a transparent tube standing in the center of the pedestal. An upper plate having an air chamber at the upper end of the transparent tube, a plurality of light sources arranged inside, and a hook for suspending a light-transmissive culture container at the upper end of the air chamber. And a first-stage culture device in which a tube communicating with the air chamber is inserted inside the culture container, and an inclined plate by fixing the upper end of the light-transmitting culture container to the upper end of the tilt stand. A second-stage culture device, which is placed on the top of the tilt stand and is connected to the air pipe installed in the upper end of the tilting stand, is inserted into the culture container, and Andon is fixed in the center of the water tank. I installed a submersible pump,
Extend the pipe for pumping the culture fluid from the submersible pump, open the tip of this pipe to the lower inside of the water tank, and eject the culture fluid in the water tank from this tip, while branching the pipe to the outside of the water tank. The method for cultivating algae according to the fifth aspect of the invention is characterized by comprising a third-stage culturing device that is in communication with each other. Part as a seed and most of it as a seed for the second step, increasing the amount of algae culture solution, preserving the seed by pure culture and supplying the seed to the second-stage culturing process. And the first stage of performing the light-transmissive culture container on the tilt stand,
The algae obtained in the first stage by the semi-closed culture method are purely cultivated, and the second stage in which the whole amount is supplied as seeds to the open system large-scale culture process in the third stage, and the submerged pump and water flow in the algae culture tank. It is equipped with a generator and the culture solution obtained in the second step is cultivated in large quantities while being rotated and stirred, and then the whole amount is harvested. It is characterized in that each step of is performed continuously.
【0005】[0005]
【作用】本発明の培養装置は、光源の周囲に配置した光
透過性の培養容器により培養した藻類の一部をその種と
して再利用し、その多くを次の段階の種として利用する
ことによりクロレラ藻類培養液量を増加させ、純粋培養
による種の保存と第二段階の培養過程への種の供給を行
う。また本発明の培養装置は、光透過性の培養容器を傾
斜スタンドに設置して、準閉鎖系培養方法により純粋培
養性を維持しながら培養し、次の段階である開放系大量
培養過程へその全量を種として供給する。また本発明の
培養装置は、藻類培養の水槽に水中ポンプと藻類水流発
生装置を設備することにより培養液を回転・攪拌させな
がら、開放系のままで藻類の大量培養を行い全量を収穫
する。また、本発明の培養装置は、上記した3発明の各
段階を一連の行程で連続して行う。すなわち、光源の周
囲に配置した光透過性の培養容器により培養した藻類の
一部をその種として再利用し、その多くを次の段階の種
として利用することによりクロレラ藻類培養液量を増加
させ、純粋培養による種の保存と第二段階の培養過程へ
の種の供給を行い、続いて、光透過性の培養容器を傾斜
スタンドに設置して、準閉鎖系培養方法により純粋培養
性を維持しながら培養し、次の段階である開放系大量培
養過程へその全量を種として供給し、次いで藻類培養の
水槽に水中ポンプと藻類水流発生装置を設備することに
より培養液を回転・攪拌させながら、開放系のままで藻
類の大量培養を行い全量を収穫する。The culturing apparatus of the present invention enables reuse of a part of algae cultivated in the light-transmissive culturing vessel arranged around the light source as its seed, and most of it as seed for the next step. Increase the amount of Chlorella algae culture broth to preserve the seeds by pure culture and supply the seeds to the second stage culture process. Further, the culture device of the present invention, a light-transmissive culture container is installed on an inclined stand, and culture is performed while maintaining pure culture by a semi-closed system culture method, and the next step is an open system mass culture process. Supply all as seeds. In addition, the culture device of the present invention is equipped with an underwater pump and an algae water flow generator in a water tank for algae culture to rotate and agitate the culture solution while performing large-scale culture of algae in an open system to harvest the whole amount. Further, the culture apparatus of the present invention continuously carries out the steps of the above-mentioned three inventions in a series of steps. That is, a part of the algae cultivated in a light-transmissive culture vessel placed around the light source is reused as its seed, and most of it is used as the seed of the next stage to increase the amount of chlorella algae culture solution. , Preservation of seeds by pure culture and supply of seeds to the second stage of the culture process, followed by installation of a light-transmissive culture container on a tilt stand to maintain pure culture by a semi-closed culture method. While culturing, the whole amount is supplied as seeds to the next stage, an open-system large-scale culturing process, and then the aqua culture tank is equipped with an underwater pump and an algae water flow generator while rotating and stirring the culture solution. , Algae are cultivated in large quantities in the open system, and the whole amount is harvested.
【0006】[0006]
【実施例】図1ないし図3に示すものは本発明の培養装
置の第一段階に使用される装置の一実施例で、種の継代
培養と中間培養に接種するまでの培養装置であり、以
下、図に基づいて説明する。下端にキャスター11をつ
けた円盤状の台座16の中央に透明アクリル管6を立設
し、その中に光源となる複数の蛍光灯7を設置する。透
明アクリル管6の上部には換気用の排出穴13を穿設し
底部には空気取り入れ穴12を開け、蛍光灯7で温めら
れて軽くなった空気を排出せしめ、透明アクリル管6内
の気温の上昇を防いでいる。1 to 3 show one embodiment of the apparatus used in the first stage of the culture apparatus of the present invention, which is a culture apparatus for inoculating seed subculture and intermediate culture. Hereinafter, description will be given with reference to the drawings. A transparent acrylic tube 6 is erected in the center of a disk-shaped pedestal 16 having casters 11 at its lower end, and a plurality of fluorescent lamps 7 serving as light sources are installed therein. A vent hole 13 for ventilation is formed in the upper part of the transparent acrylic tube 6 and an air intake hole 12 is opened in the bottom part so that the air warmed by the fluorescent lamp 7 and lightened is discharged, and the temperature inside the transparent acrylic tube 6 is discharged. Is preventing the rise of.
【0007】上記透明アクリル管6の上部には密閉した
空気室17を構成した。上記空気室17の上端に上板と
しての上部円盤3を取り付け、その周囲にクロレラ等の
藻類の培養ビニール袋5を吊り下げるためのフック4を
設置する。更に上板3の上面には培養ビニール袋5へ通
気するためのエアーポンプ1と蛍光灯7やエアーポンプ
1のスイッチを収容したスイッチボックス2、グローボ
ックス14を設ける。A closed air chamber 17 is formed above the transparent acrylic tube 6. An upper disc 3 as an upper plate is attached to the upper end of the air chamber 17, and a hook 4 for suspending a culture vinyl bag 5 of algae such as chlorella is installed around the upper disc 3. Further, on the upper surface of the upper plate 3, there are provided an air pump 1 for ventilating the culture vinyl bag 5, a switch box 2 accommodating a switch of the fluorescent lamp 7 and the air pump 1, and a glow box 14.
【0008】上記フック4に吊り下げられる培養ビニー
ル袋5は、円筒状のビニール袋を適当な長さに裁断し、
その一端を折り曲げて圧着し適当な位置にビニールチュ
ーブ8の差込み穴を開けて作成する。そして、大きさは
直径5〜15cm、長さ0.5〜1.5m程度とし、こ
れを藻類培養用光源である蛍光灯7を中心とした円の周
辺に配置した。そのため培養装置のユニット化が図られ
ると共に、培養容器が光源から等距離になったことで培
養容器毎の培養条件が均一化された。The culture vinyl bag 5 suspended from the hook 4 is obtained by cutting a cylindrical vinyl bag into an appropriate length.
One end of the vinyl tube 8 is bent and pressure-bonded to form an insertion hole for the vinyl tube 8 at an appropriate position. The size was about 5 to 15 cm in diameter and about 0.5 to 1.5 m in length, and this was arranged around a circle centered on the fluorescent lamp 7 which is a light source for algae culture. Therefore, the culture device was unitized, and the culture conditions were made uniform for each culture container because the culture container was equidistant from the light source.
【0009】上記のように構成した本実施例の作用を説
明する。まず、フック4に培養ビニール袋5を吊り下げ
る。この培養ビニール袋5内には、藻類としてクロレラ
の種と必要な量の海水等を入れておく。そして、スイッ
チを作動させエアーポンプ1からエアを透明アクリル管
6の上部の空気室17に送り込む。そしてこのエアは空
気室17からエアーコック15、ビニールチューブ8を
通って培養ビニール袋5内のエアーストーン10から通
気され、クロレラの培養が行われる。The operation of this embodiment configured as described above will be described. First, the culture vinyl bag 5 is hung on the hook 4. In this culture vinyl bag 5, chlorella seeds as algae and a necessary amount of seawater or the like are put. Then, the switch is operated to send air from the air pump 1 into the air chamber 17 above the transparent acrylic tube 6. Then, this air is aerated from the air chamber 17 through the air cock 15, the vinyl tube 8 and the air stone 10 in the culture vinyl bag 5 to culture the chlorella.
【0010】上記第一段階での種の培養は本システムの
基本となる部分であり、第二段階で使用できる培養密度
まで増殖する培養時間を一定にすることが必要である。
このため本実施例では、ビニールチューブ8を差し込む
穴から濾過海水と滅菌用塩素を注入して培養海水を一晩
静置して塩素消毒し、瀑気により脱塩素した後に栄養塩
と一定の培養初期密度となるように種を接種して培養す
る。一定の条件下で培養し、培養開始後一定日数経過し
てから収穫及びその一部を種として利用することが可能
となる。この操作を繰り返すことで、安定的に計画的に
純粋培養することが可能となった。The seed culture in the first stage is a basic part of the present system, and it is necessary to keep the culture time constant for growing to a culture density usable in the second stage.
For this reason, in this embodiment, filtered seawater and chlorine for sterilization are injected through the hole into which the vinyl tube 8 is inserted, and the culture seawater is left to stand overnight for sterilization by chlorine, and after dechlorination by waterfall, a constant culture with nutrient salts is performed. Inoculate and culture the seeds to the initial density. After culturing under a certain condition and a certain number of days after the start of culturing, the harvest and a part thereof can be used as seeds. By repeating this operation, it became possible to stably and intentionally carry out pure culture.
【0011】この第一段階の培養に使用する培養装置は
太陽光下でも使用できるが、好ましくは空調の利いた室
内での使用が望ましい。温度管理された室内で人工光を
使用することにより培養条件が一定に保たれるため、計
画的かつ安定したクロレラの培養生産を可能ならしめる
からである。本装置は培養容器にビニール袋を使用する
ことで容易に準閉鎖培養方式とすることができ、また、
キャスター11を取付けたことで、中間培養装置の設置
場所へ培養ビニール袋5を吊り下げたまま移動でき、純
粋培養された状態で第二段階の中間培養装置へ植え継ぐ
ことが可能となりかつ省力化に役立つ。The culturing apparatus used for the first-stage culturing can be used under sunlight, but it is preferable to use it in an air-conditioned room. By using artificial light in a temperature-controlled room, the culture conditions are kept constant, which allows planned and stable chlorella culture production. This device can be easily made into a semi-closed culture system by using a plastic bag for the culture container.
By attaching the casters 11, it is possible to move the culture vinyl bag 5 to the installation location of the intermediate culture device while hanging it, and it is possible to transfer it to the second-stage intermediate culture device in a pure culture state and save labor. To help.
【0012】本装置に接種する種に純粋培養種を接種す
れば、滅菌済みの培養ビニール袋5を使い捨て状態で用
いることにより、その純粋性が維持継続培養できる。装
置の材質には、目的の強度を維持できるものなら、木製
・金属製・合成樹脂製等のものを用いることができる。
また、培養容器の素材としてはビニール袋に限らず光透
過性があり強度保持のできるもので、培養対象のクロレ
ラ等の藻類に害のある物質を溶出しないものなら特に限
定はない。さらに培養ビニール袋5の大きさや形状等も
任意であり、本実施例で示したものに限定されない。If a pure culture seed is inoculated to the seeds to be inoculated into the present apparatus, the sterilized culture vinyl bag 5 can be used in a disposable state to maintain and maintain its purity. As the material of the device, wood, metal, synthetic resin or the like can be used as long as the desired strength can be maintained.
Further, the material for the culture container is not limited to a vinyl bag, and is not particularly limited as long as it is light-transmissive and capable of retaining strength, and does not elute a substance harmful to algae such as chlorella to be cultured. Further, the size and shape of the culture vinyl bag 5 are arbitrary and are not limited to those shown in this embodiment.
【0013】図4及び図5に示すものは、第二段階に使
用される中間培養装置である。本装置は、太陽光線を直
角に受光できるように、傾斜板21aを有する傾斜スタ
ンド21の上部に蝶ナット32、ボルト34及び固定プ
レート33を取り付け、これらによって培養ビニール袋
20の上端を固定する。この傾斜スタンド21上部背面
に、先端部にエアーストーン24をつけたビニールチュ
ーブ23を通して培養ビニール袋22を通気するための
エアーコック31を取り付けたエアー管26を配管す
る。このエアー管26にエアーメインバルブ27を取り
付けることにより、1〜10個の培養ビニール袋22を
1セットとした傾斜スタンド21を連結することができ
る。FIGS. 4 and 5 show an intermediate culture device used in the second stage. In this device, a wing nut 32, a bolt 34, and a fixing plate 33 are attached to the upper part of the tilt stand 21 having the tilt plate 21a so that the sun rays can be received at a right angle, and the upper end of the culture vinyl bag 20 is fixed by these. An air pipe 26 attached with an air cock 31 for ventilating the culture vinyl bag 22 is passed through a vinyl tube 23 having an air stone 24 at the tip thereof on the rear surface of the upper portion of the tilt stand 21. By attaching the air main valve 27 to the air pipe 26, the inclined stand 21 having 1 to 10 culture vinyl bags 22 as a set can be connected.
【0014】更に、傾斜スタンド21前面の底部に、上
部に散水ノズル29を有するフレキシブル管30を取り
付けた冷却水給水管25を配管し、夏期等の気温上昇時
期に冷却水を培養ビニール袋22の上に散水できるよう
にした。このため水の気化熱により培養液の水温を下げ
ることが可能となる。また、冷却水給水管25に給水メ
インバルブ28を取り付け、1〜10個の培養ビニール
袋22を1セットした傾斜スタンド21を連結すること
ができる。Further, a cooling water supply pipe 25 having a flexible pipe 30 having a water spray nozzle 29 attached to the upper portion is attached to the bottom of the front surface of the inclined stand 21, and the cooling water is supplied to the culture vinyl bag 22 in the summer when the temperature rises. I was able to sprinkle it on. Therefore, the water temperature of the culture solution can be lowered by the heat of vaporization of water. Further, a water supply main valve 28 can be attached to the cooling water supply pipe 25 to connect the inclined stand 21 having one to ten culture vinyl bags 22 set therein.
【0015】傾斜スタンド21の傾斜板21aは太陽光
線の反射率を高めるために白色もしくは銀色等のペイン
トで塗装してある。傾斜スタンド21を製作する材料は
木製に限らず、金属製、合成樹脂製、コンクリート、ブ
ロック、FRP等が利用できる。また、傾斜スタンド2
1は、培養中の培養ビニール袋22の重量に対する強度
を保持することができれば、前述の金属製等の枠に太陽
光線を反射できるシート或いはそのシートを張った網地
でも良い。The sloping plate 21a of the sloping stand 21 is coated with a paint such as white or silver in order to enhance the reflectance of sunlight. The material for forming the tilt stand 21 is not limited to wood, but metal, synthetic resin, concrete, block, FRP, or the like can be used. Also, the tilt stand 2
The sheet 1 may be a sheet that can reflect the sun's rays on the frame made of metal or the like, or a mesh sheet that stretches the sheet, as long as it can maintain the strength against the weight of the cultured vinyl bag 22 during culture.
【0016】この第二段階の中間培養装置では、前述し
た第一段階で培養した種を接種して培養する。この種に
純粋培養種を接種すれば、前装置同様、滅菌済みの培養
ビニール袋を使い捨てして用いることによりその純粋性
を維持継続して培養できる。この段階における種の植え
継ぎ前の準備、たとえば使用する海水の滅菌方法、を第
一段階と同様に行うことで、培養開始時の状態を純粋培
養に近い状態にすることができる。また、第一段階の培
養容器から第二段階の容器への種の植え継ぎは、第一段
階のエアーチューブをサイフォン管として利用すること
により行える。更に、培養容器に使い捨てビニール製袋
を用いていることから準閉鎖培養系での培養が可能にな
り、第二段階における培養の安定性と計画性が確保でき
ることになる。In this second stage intermediate culture device, the seeds cultured in the first stage described above are inoculated and cultured. When this seed is inoculated with a pure culture seed, it is possible to continuously maintain the purity by sterilizing and using a sterilized culture vinyl bag as in the previous device. By performing the preparation before seeding at this stage, for example, the sterilization method of seawater to be used, in the same manner as in the first stage, the state at the start of culture can be made close to a pure culture. Further, seeding can be transferred from the first-stage culture container to the second-stage container by using the first-stage air tube as a siphon tube. Furthermore, since the disposable vinyl bag is used as the culture container, the culture can be performed in the semi-closed culture system, and the stability and planning of the culture in the second stage can be secured.
【0017】種を植え継いた後の培養は太陽光下で行う
が、空調と人工光でコントロールした室内で培養しても
何等差し支えない。夏期の直射日光下での培養では、培
養液が高温になりクロレラの耐性温度を超える恐れがあ
るが、培養容器に散水し水の気化熱により培養液温を下
げることが可能である。After the seeds have been subcultured, the culture is carried out under sunlight, but there is no problem even if the culture is carried out in a room controlled by air conditioning and artificial light. In the culture in direct sunlight in summer, the temperature of the culture solution may rise to a temperature higher than the tolerance temperature of chlorella, but it is possible to lower the temperature of the culture solution by sprinkling water on the culture vessel and evaporating heat of water.
【0018】図6及び図7は、第三段階に使用される屋
外培養装置を示す。本装置は、半径1〜10m,水深1
〜1.5m程度の円形の水槽40の中心部分に、一方の
端に培養液吸引スリット47を入れた、半径20〜50
cm程度の塩化ビニール製のパイプ型のアンドン49を
据え付け、上部に支持ロープ45を張り渡して水槽40
に固定する。アンドン49の内部に水中ポンプ48を設
置し、水中ポンプ48の吐出口から培養液圧送用の塩化
ビニール製のパイプ41を水槽40の底面までコの字形
に配管して、その末端の噴出口46を斜め上方に向け
る。上述の装置の大きさや形状は実施例のものに限定さ
れない上記パイプ41を水槽40壁面上部の位置でT字
状に分枝させ、切り換えバルブ42をとりつけ、このバ
ルブ操作により培養液を他水槽または使用する場所へ輸
送することが容易に行える。FIGS. 6 and 7 show an outdoor culture device used in the third stage. This device has a radius of 1 to 10 m and a water depth of 1
A culture solution suction slit 47 is placed at one end in the center of a circular water tank 40 of about 1.5 m, and a radius of 20 to 50.
A vinyl chloride pipe type ANDON 49 of about cm is installed, and a supporting rope 45 is stretched over the water tank 40.
Fixed to. An underwater pump 48 is installed inside the ANDON 49, and a vinyl chloride pipe 41 for pumping the culture solution from the outlet of the underwater pump 48 to the bottom of the water tank 40 is piped in a U shape, and a jet port 46 at the end thereof. Turn diagonally upward. The size and shape of the above-mentioned device are not limited to those of the embodiment. The pipe 41 is branched into a T-shape at a position above the wall surface of the water tank 40, and a switching valve 42 is attached. It can be easily transported to the place of use.
【0019】水槽40の中心に据えた水中ポンプ48に
より培養液を吸引し、噴出口46から噴出させて水槽4
0内部の培養液を効率よく回転・撹拌させることができ
る。この屋外培養装置は開放系で使用することから培養
液中に種々のゴミが混入するので、それ等を除去する目
的でパイプ44の途中に密閉式ストレーナーを設備する
こともできる。水槽40の材質は合成樹脂・コンクリー
ト・金属・FRP等を適用し得る。また、形状も円に限
らず楕円形・8角形・6角形等水が回転しやすい形状で
あれば良い。また、夏期の高水温時にはクーリングタワ
ーを使用し、培養液をこれに通過させて気化熱の作用に
より培養液の水温を低下させることも可能である。The culture solution is sucked by a submersible pump 48 installed at the center of the water tank 40 and ejected from the ejection port 46 to make the water tank 4
It is possible to efficiently rotate and agitate the culture solution inside 0. Since this outdoor culture apparatus is used in an open system, various kinds of dust are mixed in the culture solution. Therefore, a closed strainer can be installed in the middle of the pipe 44 for the purpose of removing them. The material of the water tank 40 may be synthetic resin, concrete, metal, FRP or the like. Further, the shape is not limited to a circle, and may be any shape such as an ellipse, an octagon, or a hexagon that allows water to easily rotate. It is also possible to use a cooling tower at the time of high water temperature in summer and to pass the culture solution through it to lower the water temperature of the culture solution by the action of heat of vaporization.
【0020】第三段階の培養は、第二段階の培養液を第
三段階の培養水槽に植え継ぐ前の塩素滅菌・脱塩素の確
認から始まり、次いで種を植え継ぐ。水槽40まで届く
ホースを取付けた定量ポンプを第二段階の培養容器に挿
入し、このポンプで一定量の種を移送する。その後水槽
40の中心部に設置してある水中ポンプ48から延びた
パイプ41の先端の噴出口46で培養液を吐出させるこ
とで水槽40内の培養液を回転・撹拌させる。大型水槽
を使った従来方法による培養では、水深を深く取ること
が困難であるが、本装置では水槽40の水深を1〜1.
5mとしても十分培養可能となった。培養液の回転・撹
拌はクロレラの一つ一つの細胞を表面に出現させる確率
を高め、クロレラの光合成作用を活発ならしめ、増殖の
促進が図られることになり、培養時間の短縮と高密度化
が図られた。The third-stage culture starts with confirmation of chlorine sterilization and dechlorination before the second-stage culture solution is subcultured in the third-stage culture water tank, and then the seeds are subcultured. A metering pump equipped with a hose that reaches the water tank 40 is inserted into the second-stage culture container, and this pump transfers a certain amount of seeds. After that, the culture solution in the water tank 40 is rotated and stirred by discharging the culture solution from the jet port 46 at the tip of the pipe 41 extending from the submersible pump 48 installed at the center of the water tank 40. It is difficult to make the water depth deep by the conventional method of culturing using a large-sized water tank, but in this device, the water depth of the water tank 40 is 1 to 1.
Even when the length was 5 m, sufficient culture became possible. Rotating and stirring the culture solution increases the probability that each cell of Chlorella appears on the surface, activates the photosynthetic action of Chlorella, and promotes proliferation, shortening the culture time and increasing the density. Was planned.
【0021】このように本実施例の装置を利用した培養
方法では、第一段階で純粋培養した種クロレラを第二段
階の準閉鎖系培養方法で量の拡大を図り、第二段階で培
養した全量を第三段階の水槽40に接種する。そして、
第三段階の培養密度が使用可能なレベルに到達した段階
でその全量を使用し、その後水槽40を洗浄する。次い
で、アルコール他の消毒剤で水槽40の内部壁面・底面
を消毒後、再び水槽40に満たした海水を塩素滅菌・脱
塩素して、新たな第二段階で培養した種を接種して培養
する、という一連のシステムを稼働することにより、最
終段階は開放系ではあるが閉鎖系に準じたクロレラの安
定した大量培養方法を確立できた。As described above, in the culturing method using the apparatus of this example, the amount of seed chlorella purely cultivated in the first step was expanded by the semi-closed culturing method in the second step and cultivated in the second step. The whole amount is inoculated into the water tank 40 of the third stage. And
When the culture density in the third stage reaches a usable level, the whole amount is used, and then the water tank 40 is washed. Then, after disinfecting the inner wall surface / bottom surface of the water tank 40 with an alcohol or other disinfectant, the seawater filled in the water tank 40 is sterilized and dechlorinated again, and the seeds cultured in the new second stage are inoculated and cultured. By operating a series of systems called ",", we were able to establish a stable mass-culturing method for chlorella according to the closed system although it was an open system at the final stage.
【0022】(実施例1) 実施場所(有)奄美養魚(鹿児島県大島郡瀬戸内町久根
津) 実施時期 平成5年3月 培養した藻類の種類 海産クロレラ 栄養塩の種類 硫安 尿素 過燐酸石灰 クレワット3
2(帝国化学産業株式会社の製品) 結果 第三段階培養終了後4日間でクロレラ全量を使用。従来
方法では5トン(培養液の25%)使用後、使用した同
量の濾過海水と栄養塩を追加し元の密度に戻るまで5日
要した。クロレラが利用できるまでの時間は、従来法よ
り合計で8日間短縮でき、利用できるクロレラの細胞数
も67%アップした。(Example 1) Implementation place (existence) Amami fish farming (Kunetsu, Setouchi-cho, Oshima-gun, Kagoshima Prefecture) Implementation time March, 1993 Type of algae cultivated Marine chlorella Type of nutrient salt Ammonium sulphate Urea Superphosphate crew Crewat 3
2 (Product of Teikoku Chemical Industry Co., Ltd.) Result Use the entire amount of Chlorella within 4 days after the completion of the 3rd stage culture. In the conventional method, after using 5 tons (25% of the culture broth), it took 5 days to add the same amount of the filtered seawater and the nutrient salt used to restore the original density. The time until chlorella can be used can be shortened by 8 days in total compared to the conventional method, and the number of chlorella cells that can be used is increased by 67%.
【0023】(実施例2) 実施場所(有)A&Aハッチェリー(鹿児島県名瀬市大
字芦花部宇金久田) 実施時期 平成5年10月〜平成6年3月 培養した藻類の種類 海産クロレラ 栄養塩の種類 硫安 尿素 過燐酸石灰 クレワット3
2(帝国化学産業株式会社の製品) 実施例1と培養時期が異なっているが、ほぼ同じ結果を
得ることができた。(Example 2) Implementation place (with) A & A Hatchery (Ushikuda, Ashihanabe, Naze-shi, Kagoshima) Implementation time October, 1993-March, 1994 Type of algae cultivated Marine chlorella Nutrient salt Type Ammonium sulfate Urea Super lime lime Crewat 3
2 (Product of Teikoku Chemical Industry Co., Ltd.) Although the culture time was different from that in Example 1, almost the same results could be obtained.
【0024】[0024]
【発明の効果】クロレラ等の藻類の大量培養過程を3段
階に区分し、各段階を独立して作動せしめ、あるいは各
段階をシステム結合して大量培養することを特徴とする
本発明により、魚介類種苗生産過程で藻類を必要とする
時期に合わせた藻類の培養計画に基づいた培養が安定的
に行えるようになった。また、藻類を必要としない生産
の端境期には培養液量の少ない第一段階のみの継代を行
うことで、経費の節減を図れる。本発明の各段階の培養
条件は安定した培養条件に保つことができることから、
クロレラ等の藻類の長期に亘る大量収穫と安定培養に効
果を奏する。EFFECTS OF THE INVENTION According to the present invention, the process of mass-cultivating algae such as chlorella is divided into three stages and each stage is independently operated, or each stage is system-coupled to carry out mass culture. Cultivation based on an algae culture plan adapted to the time when algae are needed in the seedling production process has become stable. In addition, at the off-season stage of production that does not require algae, it is possible to save costs by performing only the first stage of subculture with a small amount of culture solution. Since the culture conditions of each stage of the present invention can be kept stable culture conditions,
It is effective for long-term mass harvesting and stable culture of algae such as Chlorella.
【図1】第一段階の培養装置の一部断面側面図FIG. 1 is a partial cross-sectional side view of a first-stage culture device.
【図2】第一段階の培養装置の一部切欠平面図FIG. 2 is a partially cutaway plan view of the first-stage culture device.
【図3】第一段階の培養装置の一部省略底面図FIG. 3 is a partially omitted bottom view of the first-stage culture device.
【図4】第二段階の培養装置の正面図FIG. 4 is a front view of the second-stage culture device.
【図5】第二段階の培養装置の側面図FIG. 5 is a side view of the second-stage culture device.
【図6】第三段階の培養装置の断面側面図FIG. 6 is a sectional side view of the third-stage culture device.
【図7】第三段階の培養装置の平面図FIG. 7 is a plan view of a third stage culture device.
4 フック 5 培養容器 6 透明管 7 光源 8 チューブ 20 培養容器 21 傾斜スタンド 40 水槽 41 チューブ 49 アンドン 4 hooks 5 culture vessel 6 transparent tube 7 light source 8 tube 20 culture vessel 21 tilting stand 40 water tank 41 tube 49 ANDON
Claims (5)
透明管の上端に空気室を構成すると共に内部には複数の
光源を配置し、さらに前記空気室の上端には光透過性の
培養容器を吊り下げるためのフックを備えた上板を固定
し、上記培養容器の内部には上記空気室と連通したチュ
ーブを挿入してなり、このチューブによって上記空気室
からエアを培養容器内に送りこむことを特徴とする藻類
の培養装置。1. A transparent tube is erected at the center of a pedestal, an air chamber is formed at the upper end of the transparent tube, and a plurality of light sources are arranged inside the transparent tube. The upper plate provided with a hook for suspending the culture container is fixed, and a tube communicating with the air chamber is inserted into the culture container, and air is supplied from the air chamber to the culture container by the tube. An algae culture device characterized by being sent to
器の上端を固定して傾斜板上に載置し、傾斜スタンドの
上端に設けたエアー管に連通するチューブを培養容器内
に挿入してなり、このチューブによってエアを培養容器
内に送りこむことを特徴とする藻類の培養装置。2. A light-transmissive culture container is fixed to the upper end of the tilt stand and placed on the tilt plate, and a tube communicating with an air tube provided at the upper end of the tilt stand is inserted into the culture container. The algae culture device is characterized in that air is sent into the culture container by this tube.
アンドン内部に水中ポンプを設置し、水中ポンプから培
養液圧送用のパイプを延出せしめ、このパイプの先端を
水槽の内側下方に開放せしめ、この先端から水槽内の培
養液を噴出させる一方、上記パイプを分岐して水槽の外
部と連通せしめたことを特徴とする藻類の培養装置。3. An Andon is fixed at the center of the water tank, an underwater pump is installed inside the Andon, and a pipe for feeding the culture solution is extended from the underwater pump, and the tip of this pipe is opened to the lower inside of the water tank. An apparatus for cultivating algae, characterized in that the culture solution in the water tank is jetted from this tip while the pipe is branched to communicate with the outside of the water tank.
透明管の上端に空気室を構成すると共に内部には複数の
光源を配置し、さらに前記空気室の上端には光透過性の
培養容器を吊り下げるためのフックを備えた上板を固定
し、上記培養容器の内部には上記空気室と連通したチュ
ーブを挿入してなる第一段階の培養装置と、 傾斜スタンドの上端に培養容器の上端を固定して傾斜板
上に載置し、傾斜スタンドの上端に設けたエアー管に連
通するチューブを光透過性の培養容器内に挿入してなる
第二段階の培養装置と、 水槽の中心部にアンドンを固定し、このアンドン内部に
水中ポンプを設置し、水中ポンプから培養液圧送用のパ
イプを延出せしめ、このパイプの先端を水槽の内側下方
に開放せしめ、この先端から水槽内の培養液を噴出させ
る一方、上記パイプを分岐して水槽の外部と連通せしめ
てなる第三段階の培養装置からなることを特徴とする藻
類の培養装置。4. A transparent tube is provided upright in the center of the pedestal, an air chamber is formed at the upper end of the transparent tube, and a plurality of light sources are arranged inside the transparent tube. The upper plate with a hook for suspending the culture container of is fixed, and the culture device of the first stage in which the tube communicating with the air chamber is inserted inside the culture container, and the upper end of the tilt stand. A second-stage culture device in which the upper end of the culture container is fixed and placed on an inclined plate, and a tube communicating with an air tube provided at the upper end of the inclination stand is inserted into the light-transmissive culture container. An Andon is fixed in the center of the aquarium, an underwater pump is installed inside this Andon, a pipe for pumping the culture solution is extended from the underwater pump, and the tip of this pipe is opened inside the aquarium. A method of ejecting the culture solution in the aquarium , Culture apparatus algae, comprising the culturing apparatus of the third stage comprising brought outside communicating aquarium branches of the pipe.
器により藻類を培養し、その後この藻類の一部をその種
として利用し、かつその大部分を第二段階の種として利
用することにより藻類の培養液量を増加させ、純粋培養
による種の保存と第二段階の培養過程への種の供給を行
う第一段階と、 光透過性の培養容器を傾斜スタンドに設置して、準閉鎖
系培養方法により第一段階で得られた藻類を純粋培養
し、第三段階の開放系大量培養過程へその全量を種とし
て供給する第二段階と、 藻類培養の水槽に水中ポンプと水流発生装置を設備して
第二段階で得られた培養液を回転・攪拌させながら開放
系のままで大量培養し、その後全量を収穫する第三段階
からなり、上記第一段階、第二段階、第三段階の各段階
を連続して行うことを特徴とする藻類の培養方法。5. Culturing algae in a light-transmissive culture vessel placed around a light source, and then using some of this algae as its seed and most of it as a second stage seed. To increase the amount of algae culture solution, to store the seeds in pure culture and to supply the seeds to the second stage of the culture process, and to install a light-transmissive culture vessel on the tilt stand. The algae obtained in the first stage by the closed culture method are purely cultivated, and the second stage is to supply the whole amount as seeds to the open system large-scale culture process in the third stage, and the submerged pump and water flow are generated in the algae culture tank. Equipped with a device, the culture solution obtained in the second step is cultivated and agitated in a large amount in an open system, and then the whole amount is harvested. Algae characterized by continuously performing each of the three stages Method of culturing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20790794A JPH0838156A (en) | 1994-07-28 | 1994-07-28 | Culture of alga and apparatus therefor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20790794A JPH0838156A (en) | 1994-07-28 | 1994-07-28 | Culture of alga and apparatus therefor |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0838156A true JPH0838156A (en) | 1996-02-13 |
Family
ID=16547551
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP20790794A Withdrawn JPH0838156A (en) | 1994-07-28 | 1994-07-28 | Culture of alga and apparatus therefor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0838156A (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999050384A1 (en) * | 1998-03-31 | 1999-10-07 | Micro Gaia Co., Ltd. | Fine algae culture device |
US6579714B1 (en) * | 1999-09-29 | 2003-06-17 | Micro Gaia Co., Ltd. | Method of culturing algae capable of producing phototrophic pigments, highly unsaturated fatty acids, or polysaccharides at high concentration |
KR100392914B1 (en) * | 2001-03-19 | 2003-07-28 | 라파즈 한라 시멘트 주식회사 | An internally illuminated photobioreactor for biological CO2 fixation |
JP2003529362A (en) * | 2000-04-03 | 2003-10-07 | ローテック ゲゼルシャフト フュア ビオアクティーヴェ ヴィルクシュトッフェ ミット ベシュレンクテル ハフツング | Culture device for plant or animal tissue culture |
DE102004019234B3 (en) * | 2004-04-16 | 2005-11-24 | Sartorius Ag | Bioreactor for the cultivation of microorganisms |
DE102009028474A1 (en) * | 2009-08-12 | 2011-02-17 | Igv Institut Für Getreideverarbeitung Gmbh | Device and method for the production of biomass |
KR101017501B1 (en) * | 2007-07-20 | 2011-02-25 | 박철완 | A intensification method of nutrition for chlorella shellfish or sea squirt |
JP2012034609A (en) * | 2010-08-05 | 2012-02-23 | Shimizu Corp | Tube-type algae-culturing device |
CN113302275A (en) * | 2019-01-15 | 2021-08-24 | 叶玛亚有限公司 | Expandable photosynthetic microorganism production and culture system |
WO2022123032A1 (en) * | 2020-12-11 | 2022-06-16 | Université d’Aix Marseille | Cell culture system, method and assembly |
WO2024190605A1 (en) * | 2023-03-14 | 2024-09-19 | 株式会社ちとせ研究所 | Culture apparatus |
-
1994
- 1994-07-28 JP JP20790794A patent/JPH0838156A/en not_active Withdrawn
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6348347B1 (en) * | 1998-03-31 | 2002-02-19 | Micro Gaia Co., Ltd. | Fine algae culture device |
WO1999050384A1 (en) * | 1998-03-31 | 1999-10-07 | Micro Gaia Co., Ltd. | Fine algae culture device |
US6579714B1 (en) * | 1999-09-29 | 2003-06-17 | Micro Gaia Co., Ltd. | Method of culturing algae capable of producing phototrophic pigments, highly unsaturated fatty acids, or polysaccharides at high concentration |
JP2003529362A (en) * | 2000-04-03 | 2003-10-07 | ローテック ゲゼルシャフト フュア ビオアクティーヴェ ヴィルクシュトッフェ ミット ベシュレンクテル ハフツング | Culture device for plant or animal tissue culture |
KR100392914B1 (en) * | 2001-03-19 | 2003-07-28 | 라파즈 한라 시멘트 주식회사 | An internally illuminated photobioreactor for biological CO2 fixation |
DE102004019234B3 (en) * | 2004-04-16 | 2005-11-24 | Sartorius Ag | Bioreactor for the cultivation of microorganisms |
KR101017501B1 (en) * | 2007-07-20 | 2011-02-25 | 박철완 | A intensification method of nutrition for chlorella shellfish or sea squirt |
DE102009028474A1 (en) * | 2009-08-12 | 2011-02-17 | Igv Institut Für Getreideverarbeitung Gmbh | Device and method for the production of biomass |
JP2012034609A (en) * | 2010-08-05 | 2012-02-23 | Shimizu Corp | Tube-type algae-culturing device |
CN113302275A (en) * | 2019-01-15 | 2021-08-24 | 叶玛亚有限公司 | Expandable photosynthetic microorganism production and culture system |
WO2022123032A1 (en) * | 2020-12-11 | 2022-06-16 | Université d’Aix Marseille | Cell culture system, method and assembly |
FR3117505A1 (en) * | 2020-12-11 | 2022-06-17 | Université d’Aix Marseille | System, method and assembly for cell culture |
WO2024190605A1 (en) * | 2023-03-14 | 2024-09-19 | 株式会社ちとせ研究所 | Culture apparatus |
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