JPS6274280A - Cultivation of alga of genus spirulina - Google Patents

Cultivation of alga of genus spirulina

Info

Publication number
JPS6274280A
JPS6274280A JP21093485A JP21093485A JPS6274280A JP S6274280 A JPS6274280 A JP S6274280A JP 21093485 A JP21093485 A JP 21093485A JP 21093485 A JP21093485 A JP 21093485A JP S6274280 A JPS6274280 A JP S6274280A
Authority
JP
Japan
Prior art keywords
spirulina
culture medium
medium
blue
extraction
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
JP21093485A
Other languages
Japanese (ja)
Other versions
JPH0262233B2 (en
Inventor
Misaki Kubota
久保田 美咲
Takashi Kotanino
喬 小谷野
Kazutaka Shinohara
篠原 和毅
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.)
Tonen General Sekiyu KK
Original Assignee
Toa Nenryo Kogyyo KK
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 Toa Nenryo Kogyyo KK filed Critical Toa Nenryo Kogyyo KK
Priority to JP21093485A priority Critical patent/JPS6274280A/en
Publication of JPS6274280A publication Critical patent/JPS6274280A/en
Publication of JPH0262233B2 publication Critical patent/JPH0262233B2/ja
Granted legal-status Critical Current

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  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

PURPOSE:To obtain a blue-green alga of the genus Spirulina in a large amount using a readily preparable culture medium, by cultivating the blue-green alga in the culture medium containing a hot water extract of fowl droppings as a nutrient source. CONSTITUTION:A blue-green alga of the genus Spirulina, e.g. Spirulina platensis, Spirulina maxima, Spirulina subsalsa, etc., is cultivated in a readily preparable culture medium containing a hot water extract of fowl droppings as a nutrient source. Sodium hydrogencarbonate is, as necessary, added to the culture medium. The amount of the algal bodies which can be obtained in the culture medium containing both the hot water extract of fowl droppings and the sodium hydrogencarbonate is equal to or more than that obtained in a conventional complicated synthetic culture medium.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発明はスピルリナ属藍藻の新規な培養方法に関する
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a novel method for culturing blue-green algae of the genus Spirulina.

〔従来の技術〕[Conventional technology]

スピルリナ属藍藻は蛋白質、β−カロチン、ビタミン類
等を多量に含み栄養のバランスが良いため食品、飼料等
の原料として用いられている。さらに将来の宇宙ステー
ションにおける酸素供給源、食料等としても期待され、
そのための研究が行われている。
Blue-green algae of the genus Spirulina contain large amounts of protein, β-carotene, vitamins, etc. and have a good nutritional balance, so they are used as raw materials for foods, feeds, and the like. Furthermore, it is expected to be used as an oxygen supply source, food, etc. for future space stations.
Research is being conducted for this purpose.

従来スピルリナ属藍藻は、例えば[藻煩研究法j197
9年、井守出版、299頁に記載されているように、多
数の無機塩類を含んでなる複雑な811成の合成培地に
よって培養されていた。しかしながら、このような培地
は多数の成分を含むためその調製が煩雑で時間を要し、
培地のコストJ)比較的高いものとなっていた。従って
、スピルリナ属藍藻を工業的に大量に培養するために適
当な培地と、これを用いる培養方法の開発が望まれてい
た。
Conventionally, blue-green algae of the genus Spirulina are
As described in 1999, Imori Publishing, p. 299, it was cultured using a complex 811 synthetic medium containing a large number of inorganic salts. However, since such a medium contains many components, its preparation is complicated and time-consuming;
Cost of culture medium J) It was relatively high. Therefore, it has been desired to develop a medium suitable for industrially cultivating large amounts of Spirulina blue-green algae and a culture method using the medium.

〔発明が解決しようとする問題点) この発明は、安価な原料を用いて部用な方法で調製する
ことができる培地を用いてスピルリナ属藍藻を培養する
方法を提供しようとするものである。
[Problems to be Solved by the Invention] The present invention aims to provide a method for culturing Spirulina cyanobacteria using a medium that can be prepared by a simple method using inexpensive raw materials.

〔問題点を解決するための手段〕[Means for solving problems]

上記の問題点は、鶏糞熱水抽出物を栄養7原として含有
し場合Gこよってはさらに炭酸水素ナトリウムを含有す
る培地中でスピルリナ属E藻を培養することを特徴とす
るこの発明の方法により解決される。
The above problem can be solved by the method of the present invention, which is characterized in that Spirulina sp. resolved.

この発明において使用する鶏糞は養鶏場から直接得られ
る生鶏糞でもよく、またこれを加熱等の方法により乾燥
した乾燥鶏糞でもよい。生鶏糞を使用する場合は抽出に
際し抽出媒体中でQQ状にほぐすのが好ましく、乾燥鶏
糞の場合には、抽出操作の前に一旦粉砕するのが好まし
い。
The chicken manure used in this invention may be raw chicken manure obtained directly from a poultry farm, or may be dried chicken manure obtained by drying it by heating or the like. When using raw chicken manure, it is preferable to loosen it in a QQ shape in an extraction medium during extraction, and in the case of dried chicken manure, it is preferable to crush it once before the extraction operation.

抽出媒体としては熱水を使用するのが好ましい。Preference is given to using hot water as extraction medium.

抽出操作における鶏糞と抽出媒体との比率は特に限定さ
れないが、乾燥鶏糞を使用する場合、抽出媒体11に対
して乾燥鶏糞0.5g〜300gとするのが好ましく、
生鶏糞を使用する場合は、抽出媒体11に対して上記の
乾燥重量に相当する量を用いるのが好ましい。抽出時に
おける鶏糞濃度が低すぎれば多量の抽出液を処理しなけ
ればならず、大きな抽出設備を必要とし、多量の熱を必
要とする等の点において経済的でない。また抽出時にお
ける鶏糞濃度が高すぎると、抽出効率が低下する。
The ratio of chicken manure and extraction medium in the extraction operation is not particularly limited, but when dry chicken manure is used, it is preferably 0.5 g to 300 g of dry chicken manure to the extraction medium 11,
When using raw chicken manure, it is preferable to use an amount corresponding to the above dry weight for the extraction medium 11. If the concentration of chicken manure at the time of extraction is too low, a large amount of extract liquid must be processed, large extraction equipment is required, and a large amount of heat is required, which is uneconomical. Furthermore, if the concentration of chicken manure during extraction is too high, the extraction efficiency will decrease.

抽出温度は70℃〜130°Cの範囲でよく、90°C
〜100℃の範囲が好ましく、沸瞠温度又はこれに近い
温度が最も好ましい。抽出時間は抽出温度により異るが
1〜5時間が好ましく、2〜3時間が特に好ましい。抽
出時間を短かくする場合、抽出温度を高温、例えば12
0℃にすればよく、この操作は耐圧容器中で行うことが
できる。
The extraction temperature may range from 70°C to 130°C, and 90°C
A range of from 100°C to 100°C is preferred, and a temperature at or near boiling temperature is most preferred. The extraction time varies depending on the extraction temperature, but is preferably 1 to 5 hours, particularly preferably 2 to 3 hours. If you want to shorten the extraction time, increase the extraction temperature to a high temperature, e.g.
The temperature may be 0° C., and this operation can be performed in a pressure-resistant container.

抽出後、抽出混合物を遠心分離、濾過等の常法に従って
固形物と抽出液とに分離する。分離の際の温度は特に限
定されない。
After extraction, the extraction mixture is separated into solid matter and extract liquid by conventional methods such as centrifugation and filtration. The temperature during separation is not particularly limited.

前記のようにして得られた抽出液中の抽出物)農度が適
切な場合には、これをそのまま培地として使用すること
ができ、又はこれに炭酸水素ナトリウムを加えた後培地
として使用することができる。
The extract in the extract obtained as described above) can be used as a medium as it is if the agricultural content is appropriate, or it can be used as a medium after adding sodium bicarbonate to it. I can do it.

また、前記の抽出液中の抽出物4度が高い場合には、こ
の抽出液を水で希釈して適当な4度とした後、又はこの
希釈液にさらに炭酸水素ナトリウムを添加した後、これ
を培地として使用する。さらに、前記の抽出液を凍結乾
燥、噴霧乾燥等の常法に従って乾燥して固体として貯蔵
することができ、必要に応じてこの乾燥物を水に溶解し
、又はこの溶液に炭酸水素ナトリウムを添加して培地を
調製することができる。
In addition, if the extract 4% in the above-mentioned extract is high, after diluting this extract with water to an appropriate 4%, or after further adding sodium bicarbonate to this diluted solution, is used as a medium. Furthermore, the above-mentioned extract can be dried by a conventional method such as freeze drying or spray drying and stored as a solid, and if necessary, this dried product can be dissolved in water or sodium bicarbonate can be added to this solution. A culture medium can be prepared by

培地中の鶏糞抽出物の量又は濃度は、その抽出物が由来
する乾燥鶏糞の量によって定義するのが便利である。こ
のようにして定義した場合、培地14当り、乾燥鶏糞0
.1〜Log、好ましくは2〜4gに由来する抽出物を
含有する培地を3jl Fする。培地に炭酸水素ナトリ
ウムを添加する場合、その添加量は約30g/β以下の
範囲で適宜選択すればよく、約20g/j!〜10g/
lの範囲で添加するのが好ましい。培地中のpHは7〜
12、好ましくは8.5〜10.5の範囲とする。上記
のようにして調製した培地は通常この範囲内のpHを有
するが、pHが低すぎる場合は例えば炭酸水素ナトリウ
ムを加えることにより、そしてp Hが高すぎる場合は
二酸化炭素を通すことにより適切な範囲に調整すること
ができる。
The amount or concentration of chicken manure extract in the culture medium is conveniently defined by the amount of dried chicken manure from which the extract is derived. When defined in this way, 0 dried chicken manure per 14 medium
.. Culture medium containing extract derived from 1 to Log, preferably 2 to 4 g, is 3jl F. When adding sodium bicarbonate to the culture medium, the amount added may be appropriately selected within the range of about 30 g/β or less, and about 20 g/j! ~10g/
It is preferable to add in a range of 1. The pH in the medium is 7~
12, preferably in the range of 8.5 to 10.5. The medium prepared as described above usually has a pH within this range, but if the pH is too low it can be adjusted to an appropriate level, for example by adding sodium bicarbonate, and if the pH is too high it can be adjusted to an appropriate pH by passing carbon dioxide. Can be adjusted to the range.

本発明の方法により培養することができるスピルリナ属
藻類としては、例えばスピルリナ・プラテンシス(Sp
irulina platensis) 、スピルリナ
・マキシマ(Spirulina maxima)、ス
ピルリナ・サブサルサ(Spirulina 5ubs
alsa)等を挙げることができる。培養温度は一般に
20゛C〜50℃の範囲であり、25℃〜45℃の範囲
が好ましい。最適培養温度はスピルリナの種類により異
り、例えばスピルリナ・プラテンシスの場合は約30℃
、スピルリナ・サブサルサの場合は約40℃が最適であ
る。培養に当っては光を照射する必要があり、この光と
して自然光(太陽光線)を使用するのが好ましいが、例
えば蛍光灯等の人工光源を使用することもできる。光照
射の強度は培養液表面においてlXIO3〜lXIO3
ルクスとするのが好ましく、7X10’〜1.5X10
’ルクスとするのがさらに好ましい。
Examples of Spirulina algae that can be cultured by the method of the present invention include Spirulina platensis (Sp
irulina platensis), Spirulina maxima, Spirulina subsalsa (Spirulina 5ubs)
alsa), etc. The culture temperature generally ranges from 20°C to 50°C, preferably from 25°C to 45°C. The optimal culture temperature varies depending on the type of Spirulina, for example, approximately 30°C for Spirulina platensis.
For Spirulina Subsalsa, approximately 40°C is optimal. In culturing, it is necessary to irradiate light, and it is preferable to use natural light (sunlight) as this light, but it is also possible to use an artificial light source such as, for example, a fluorescent lamp. The intensity of light irradiation varies from lXIO3 to lXIO3 on the culture solution surface.
Lux is preferably 7X10' to 1.5X10
It is more preferable to use 'lux'.

光の照射強度が高い場合、十分な攪(↑を行ってスピル
リナの枯死を最少限にするのが望ましい。人工光源を用
いて光を照射する場合、照射時間を1日10〜14時間
として天然光に近いサイクルで間欠照射してもよく、又
連続照射してもよい。
When the intensity of light irradiation is high, it is desirable to minimize the death of Spirulina by thoroughly stirring (↑).When irradiating light using an artificial light source, the irradiation time should be set for 10 to 14 hours a day, so that the natural Intermittent irradiation may be performed with a cycle close to that of light, or continuous irradiation may be performed.

次に実施例によりこの発明の方法をさらに具体的に説明
する。
Next, the method of the present invention will be explained in more detail with reference to Examples.

スJ1舛 市販の乾燥鶏糞30gに芳留水200m1を加え、3時
間煮沸し、東洋濾祇嵐5Aで濾過し、鶏糞抽出物を含有
する抽出液を得た。
200 ml of distilled water was added to 30 g of commercially available dried chicken manure, boiled for 3 hours, and filtered through Toyo Filter Giran 5A to obtain an extract containing a chicken manure extract.

次に、この抽出液を用いて次の組成の培地を調製した。Next, a medium having the following composition was prepared using this extract.

(培地Cは蒸留水のみ) さらに、比較のため次の組成を有する公知の合成培地(
SOT培地)を調製した。
(Medium C is only distilled water) Furthermore, for comparison, a known synthetic medium with the following composition (
SOT medium) was prepared.

Na1lCO31,680m g KzllPOn           50m gNa
NO:+           250m gK2SO
t           100m gNaC1210
0m g MgSO4−782020m g CaC(! z ・211.0           
 4m gFeSO4・7820          
   1m gNazlEDTA  ・ 2tlzO8
m  g八、 金□に虱l昆合ン夜+*′      
    Q、l m (!1留水         9
9.9mJ(*) A S金属混合液 HffB(h           286m gMn
SO4・IHzo        250m gZnS
Oa ・7Hz0       22.2m gCII
SO4−5Hz8       7.9m gNaJo
042.1 m g 蒸留水         100rr+7!上記の4種
類の培地300 m 7!ずつを1,000m12容の
L字形培養管に入れ、これにスピルリナ・サブラルサの
種藻0.06gを接種し、37°C17000ルクスの
人工照明下で12日間培養した。ごの培養液から、濾過
により藻体を回収し、真空乾燥器中で56℃にて24時
間乾燥した後、乾燥藻体の重量を測定した結果は次の通
りであった。
Na1lCO31,680m g KzllPOn 50m gNa
NO:+250m gK2SO
t 100m gNaC1210
0mg MgSO4-782020mg CaC(!z ・211.0
4m gFeSO4・7820
1m gNazlEDTA・2tlzO8
m g8, Friday night+*'
Q, l m (!1 distilled water 9
9.9mJ (*) A S metal mixture HffB (h 286m gMn
SO4・IHzo 250m gZnS
Oa ・7Hz0 22.2m gCII
SO4-5Hz8 7.9m gNaJo
042.1 mg distilled water 100rr+7! 300 m 7 of the above four types of culture media! Each was placed in a 1,000 m2 L-shaped culture tube, inoculated with 0.06 g of Spirulina sublarsa seed algae, and cultured for 12 days at 37° C. under artificial lighting of 17,000 lux. The algal bodies were collected from the culture solution by filtration, dried in a vacuum dryer at 56°C for 24 hours, and the weight of the dried algal bodies was measured.The results were as follows.

A        0.69 B        O,25 C0,06 以上の通り、きわめて而単に調製することができる本発
明の培地によりスピルリナ属藻類を培養することができ
、特に鶏糞抽出物と炭酸水素ナトリウムの両者を含有す
る本発明の培地を用いる場合、従来の複雑な合成培地で
培養した場合と同様か又はそれより多くの藻体を得るこ
とができる。
A 0.69 B O,25 C0,06 As described above, Spirulina algae can be cultured using the medium of the present invention, which can be prepared very simply, and in particular, the medium containing both chicken manure extract and sodium bicarbonate. When using the culture medium of the present invention, it is possible to obtain the same amount of algae as or more than when culturing in a conventional complex synthetic medium.

Claims (1)

【特許請求の範囲】[Claims] 1、鶏糞熱水抽出物を栄養源として含有し場合によって
はさらに炭酸水素ナトリウムを含有する培地中でスピル
リナ属藍藻を培養することを特徴とするスピルリナ属藍
藻の培養方法。
1. A method for culturing blue-green algae of the genus Spirulina, which comprises culturing the blue-green algae of the genus Spirulina in a medium containing a hot water extract of chicken manure as a nutrient source and optionally further containing sodium bicarbonate.
JP21093485A 1985-09-26 1985-09-26 Cultivation of alga of genus spirulina Granted JPS6274280A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21093485A JPS6274280A (en) 1985-09-26 1985-09-26 Cultivation of alga of genus spirulina

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21093485A JPS6274280A (en) 1985-09-26 1985-09-26 Cultivation of alga of genus spirulina

Publications (2)

Publication Number Publication Date
JPS6274280A true JPS6274280A (en) 1987-04-06
JPH0262233B2 JPH0262233B2 (en) 1990-12-25

Family

ID=16597503

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21093485A Granted JPS6274280A (en) 1985-09-26 1985-09-26 Cultivation of alga of genus spirulina

Country Status (1)

Country Link
JP (1) JPS6274280A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008153255A1 (en) * 2007-06-14 2008-12-18 Korea Research Institute Of Bioscience And Biotechnology Spirulina platensis m20cjk3 [kctc11127bp] characterized by enhanced floatation of its algal clump

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5135473A (en) * 1974-08-19 1976-03-25 Sosa Tekusukoko Sa Soruinoseichoo sokushinsaseruhoho
JPS5145453A (en) * 1974-10-15 1976-04-17 Asahi Chemical Ind SORUINYORUCHITSUSOKAGOBUTSUNO JOKYOHOHO
JPS554394A (en) * 1978-06-26 1980-01-12 Bayer Ag Manufacture of mandelic ester
JPS59213386A (en) * 1983-05-17 1984-12-03 Riyuukiyuu Sekiyu Kk Cultivation of spirulina belonging to cyanophyceae

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5135473A (en) * 1974-08-19 1976-03-25 Sosa Tekusukoko Sa Soruinoseichoo sokushinsaseruhoho
JPS5145453A (en) * 1974-10-15 1976-04-17 Asahi Chemical Ind SORUINYORUCHITSUSOKAGOBUTSUNO JOKYOHOHO
JPS554394A (en) * 1978-06-26 1980-01-12 Bayer Ag Manufacture of mandelic ester
JPS59213386A (en) * 1983-05-17 1984-12-03 Riyuukiyuu Sekiyu Kk Cultivation of spirulina belonging to cyanophyceae

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008153255A1 (en) * 2007-06-14 2008-12-18 Korea Research Institute Of Bioscience And Biotechnology Spirulina platensis m20cjk3 [kctc11127bp] characterized by enhanced floatation of its algal clump

Also Published As

Publication number Publication date
JPH0262233B2 (en) 1990-12-25

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