JPH01187082A - Production of astaxanthin-rich chlorophyceae - Google Patents

Production of astaxanthin-rich chlorophyceae

Info

Publication number
JPH01187082A
JPH01187082A JP63012328A JP1232888A JPH01187082A JP H01187082 A JPH01187082 A JP H01187082A JP 63012328 A JP63012328 A JP 63012328A JP 1232888 A JP1232888 A JP 1232888A JP H01187082 A JPH01187082 A JP H01187082A
Authority
JP
Japan
Prior art keywords
astaxanthin
culture
chlorophyceae
chlorella
salts
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
JP63012328A
Other languages
Japanese (ja)
Other versions
JP2707572B2 (en
Inventor
Shuzo Takada
高田 周三
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.)
KURORERA KOGYO KK
Chlorella Industry Co Ltd
Original Assignee
KURORERA KOGYO KK
Chlorella Industry Co Ltd
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 KURORERA KOGYO KK, Chlorella Industry Co Ltd filed Critical KURORERA KOGYO KK
Priority to JP63012328A priority Critical patent/JP2707572B2/en
Publication of JPH01187082A publication Critical patent/JPH01187082A/en
Application granted granted Critical
Publication of JP2707572B2 publication Critical patent/JP2707572B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

PURPOSE:To obtain the subject chlorophyceae in a simple culture process by making a culture of the chlorophyceae capable of bio-synthesis of astaxanthin in a culture medium containing sodium-, potassium- and/or rabidium-salts. CONSTITUTION:The objective chlorophyceae can be obtained by making a culture of the chorophyceae capable of biosynthesis of astaxanthin in a culture medium containing 0.2-1M of at least one kind of sodium salts, potassium salts and rabidium salts. The chlorophyceae to be used as the starting material is, e.g., Chlamydomonas, Hematocaccus, Ankistrodesmus, Chlorella, Chlorococcum, Coelastrum, Crucigenia, Dictyococcus, Scenedesmus, Scotiella, Protosiphon. Among then, e.g., Chlorella and Scenedesmus have already been used as foods, thus being free from any problem in respect of safety. Moreover, for the above Chlorophyceae, mass culture technology has been established, therefore, they are preferably applicable to the present production process.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発明はアスタキサンチンを高濃度で含有する緑藻類
の生産方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] This invention relates to a method for producing green algae containing astaxanthin at a high concentration.

〔従来の技術〕[Conventional technology]

赤色色素のアスタキサンチンはカロチノイド系色素の一
種で、動物界に広く分布している。カニやエビ等の甲殻
類の赤味はこのアスタキサンチンであり、水産業界では
、カニやエビの殻を鯛、錦鯉、エビの色(赤色)あげに
用いている。食品業界では古くより、センベイ等にエビ
やカニをそのままか、粉末として添加し、風味付け、色
付けなどに利用しており、最近ではめん類、パン等にも
使われ始めている。いずれも色付け1色あげに効果のあ
るのはアスタキサンチンである。またアスタキサンチン
は、β−カロチンのようなビタミンA効力を持たないが
、最近ではβ−カロチンより強い免疫賦活作用および腫
瘍排除(縮少)作用も確認されており、有用色素として
の価値が高まりつつある。
The red pigment astaxanthin is a type of carotenoid pigment that is widely distributed in the animal kingdom. Astaxanthin is responsible for the red color of crustaceans such as crabs and shrimp, and in the seafood industry, crab and shrimp shells are used to give the red color to sea bream, Nishikigoi, and shrimp. For a long time in the food industry, shrimp and crab have been added to foods such as Senbei, either as they are or as a powder, to add flavor and color, and recently they have also begun to be used in noodles, bread, etc. In both cases, astaxanthin is effective in increasing color by one color. Furthermore, although astaxanthin does not have the same vitamin A efficacy as β-carotene, it has recently been confirmed that it has a stronger immunostimulatory effect and tumor elimination (reduction) effect than β-carotene, and its value as a useful pigment is increasing. be.

しかし、アスタキサンチンの天然資源として現在利用さ
れているのは、主としてカニ、エビ、オキアミ等の殻で
あるが、これらに含まれるアスタキサンチン含量は低く
、乾燥物1gあたり0.1〜0.5醜gでしかなく、ま
た動物や人が利用(食)しやすいものではない。
However, the shells of crabs, shrimp, krill, etc. are currently used as natural resources for astaxanthin, but the astaxanthin content contained in these is low, with 0.1 to 0.5 g of astaxanthin per 1 g of dry matter. Moreover, it is not something that animals or people can easily use (eat).

一方、緑藻類は通常アスタキサンチンは含有しないか、
含有しても極めて微量であることが定説になっている。
On the other hand, green algae usually do not contain astaxanthin or
It is a well-established theory that even if it is contained, it is in extremely small amounts.

しかしいくつかの緑藻類は異常な生存環境下1例えば窒
素等の栄養欠乏環境下ではアスタキサンチンを生合成す
る。例えば緑藻へマドコツカス(Hae+5atoco
ccus)はN欠乏培養で多量に、アスタキサンチンを
含有(2mg/g)することが知られており、実験的に
培養され、エビや鯛の色あげ飼料として有効であると報
告されている。また現在、大量培養され、食品として利
用されている緑藻のクロレラやセネデスムスも、N欠乏
またはマグネシウム欠乏培養すればアスタキサンチンを
生合成することが知られており、このときのアスタキサ
ンチンの含有量はおおよそ0.5〜1.5mg/gであ
る。
However, some green algae biosynthesize astaxanthin under abnormal survival conditions, such as environments lacking nutrients such as nitrogen. For example, Hae+5atococus
Ccus) is known to contain a large amount of astaxanthin (2 mg/g) in N-deficient culture, and has been experimentally cultured and reported to be effective as color-enhancing feed for shrimp and sea bream. In addition, the green algae Chlorella and Scenedesmus, which are currently cultivated in large quantities and used as food, are known to biosynthesize astaxanthin if cultured in N- or magnesium-deficient cultures, and the astaxanthin content at this time is approximately 0. .5 to 1.5 mg/g.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

しかしながら上記の方法によって培養される緑藻類に含
まれるアスタキサンチンの含有量は必ずしも多いという
ことはできず、工業的な利用には適していないという問
題点があった。
However, the content of astaxanthin contained in green algae cultured by the above method cannot necessarily be said to be high, and there is a problem that it is not suitable for industrial use.

この発明の目的は、上記問題点を解決するため、簡単な
培養方法により、アスタキサンチンを高濃度に含有する
緑藻類の生産方法を提供することである。
An object of the present invention is to provide a method for producing green algae containing astaxanthin at a high concentration by a simple culture method in order to solve the above-mentioned problems.

〔課題を解決するための手段〕[Means to solve the problem]

この発明は、アスタキサンチンを生合成する緑藻類を、
ナトリウム塩、カリウム塩およびルビジウム塩から選ば
れる1種以上を0.2〜IM含む培地中で培養すること
を特徴とするアスタキサンチン高含有緑藻類の生産方法
である。
This invention uses green algae that biosynthesize astaxanthin.
This is a method for producing green algae with a high content of astaxanthin, which is characterized by culturing in a medium containing 0.2 to IM of one or more selected from sodium salts, potassium salts, and rubidium salts.

本発明において培養の対象となる緑藻類は、アスタキサ
ンチンを生合成する緑藻類であって、表1に属するもの
があげられる。
The green algae to be cultured in the present invention are green algae that biosynthesize astaxanthin, and include those listed in Table 1.

表1 緑藻類以外の藻類、例えば大量培養生産されている食用
藻のスピルリナ(藍藻類)やいわゆる海産クロレラ(分
類学上、緑藻類ではなく、クロレラとは別な藻類である
)では、いずれもN欠乏培養や本発明の培養法によって
もアスタキサンチンは生合成されない。
Table 1 Algae other than green algae, such as Spirulina (blue-green algae), an edible algae that is produced in large quantities, and so-called marine chlorella (taxonomically speaking, it is not a green algae but a different algae from chlorella) are both N-deficient. Astaxanthin is not biosynthesized by culture or the culture method of the present invention.

上記緑藻類の中では、クロレラ、セネデスムスなどはす
でに食品として利用されているため、安全性の面から問
題はなく、しかも大量培養技術も確立しているので、本
発明に適用するのが好ましい。
Among the above-mentioned green algae, Chlorella, Scenedesmus, etc. are already used as foods, so there is no problem from a safety perspective, and mass culture technology has been established, so it is preferable to apply them to the present invention.

このうちクロレラについては、クロレラ・フスカ(=ク
ロレラピレノイドーサ)(Chloralla fus
ca(=Chlorella pyrenoidosa
))、クロレラ拳ゾーフインゲンシス(Chlorel
la zofingiensis)、クロレラ・ホモス
ポーラ(Chlorella homosphaera
)等がアスタキサンチンを生合成する。セネデスムスそ
の他の属についてはほとんどの種がアスタキサンチンを
生合成する。
Of these, Chlorella fusca (= Chlorella pyrenoidosa)
ca (= Chlorella pyrenoidosa
)), Chlorella fistula
la zofingiensis), Chlorella homospora (Chlorella homosphaera)
) etc. biosynthesize astaxanthin. Most species of Scenedesmus and other genera biosynthesize astaxanthin.

本発明では上記のようなアスタキサンチンを生合成する
緑藻類を、ナトリウム塩、カリウム塩およびルビジウム
塩から選ばれる1種以上の塩を0.2〜IM含む培地中
で培養することにより、アスタキサンチンを生合成させ
、高濃度にアスタキサンチンを含有する緑藻類を生産す
ることができる。
In the present invention, astaxanthin can be biosynthesized by culturing the green algae that biosynthesize astaxanthin as described above in a medium containing 0.2 to IM of one or more salts selected from sodium salt, potassium salt, and rubidium salt. It is possible to produce green algae containing astaxanthin at a high concentration.

上記の塩としては、塩化物、硝酸塩、硫酸塩などがあげ
られる。
Examples of the above salts include chlorides, nitrates, and sulfates.

緑藻類の培養方法は、従来よりクロレラ、セネデスムス
等の培養に採用されている方法が適用可能である。
As a method for culturing green algae, methods conventionally employed for culturing Chlorella, Scenedesmus, etc. can be applied.

クロレラやセネデスムスの大量培養は光(太陽光)照射
下で行われているのが大部分であるが。
Most of the mass cultivation of Chlorella and Scenedesmus is carried out under light (sunlight) irradiation.

全く光を必要としない従属栄養培養も可能である。Heterotrophic culture, which requires no light at all, is also possible.

前者は開放攪拌培養、後者はタンク培養と一般に呼ばれ
ているが、いずれの培養においても本発明を適用するこ
とができる。これらの培養に際してナトリウム塩、カリ
ウム塩、ルビジウム塩等を0.2〜IM培地に添加すれ
ば1通常の培養に比べてクロレラやセネデスムス等の増
殖速度ははるかに低下する。このためアスタキサンチン
の生合成は促進されるが、生産量では緑藻の増加は期待
できない。したがってまず通常使用される培地(窒素源
、リン酸源、カリウム、マグネシウム、鉄および他の微
量金属元素を含む公知の培地)を使用し、炭酸ガス、酢
酸、ブドウ糖等を炭素源として開放攪拌培養またはタン
ク培養により大量培養し、その後ナトリウム塩、カリウ
ム塩、ルビジウム塩等を0.2〜IM濃度で添加し、培
養を続けるのがよい。
The former is generally called open agitation culture, and the latter is generally called tank culture, but the present invention can be applied to either type of culture. If sodium salts, potassium salts, rubidium salts, etc. are added to the 0.2 to IM medium during these cultures, the growth rate of Chlorella, Scenedesmus, etc. will be much lower than in normal culture. As a result, astaxanthin biosynthesis is promoted, but an increase in green algae cannot be expected in terms of production. Therefore, first, a commonly used medium (known medium containing nitrogen source, phosphoric acid source, potassium, magnesium, iron, and other trace metal elements) is used, and open agitation culture is performed using carbon dioxide gas, acetic acid, glucose, etc. as a carbon source. Alternatively, it is preferable to carry out mass culture by tank culture, and then add sodium salt, potassium salt, rubidium salt, etc. at a concentration of 0.2 to IM, and continue culturing.

はぼ4日間でクロレラや、セネデスムス等の緑藻類はア
スタキサンチンを高濃度に含有するようになり、培養液
は赤色となる。この時、窒素欠乏あるいはマグネシウム
欠乏等の栄養欠乏状態を組合せることも可能であり、こ
れによりアスタキサンチンの生合成は若干促進され、培
養日数の短縮がみられる。
Within four days, green algae such as Chlorella and Scenedesmus begin to contain astaxanthin at a high concentration, and the culture solution turns red. At this time, it is also possible to combine a nutritional deficiency state such as nitrogen deficiency or magnesium deficiency, which slightly accelerates astaxanthin biosynthesis and shortens the number of culture days.

こうして生産されたアスタキサンチン高含有緑藻類はア
スタキサンチンを4〜lo+sg/g含有し、その含有
量は栄養欠乏培養の4〜10倍の高含有承である。得ら
れた藻体は従来の藻体処理と同様に処理され、アスタキ
サンチン高含有藻体としてそのまま利用されるか、ある
いは藻体からアスタキサンチンを抽出して利用される。
The astaxanthin-rich green algae produced in this way contains astaxanthin from 4 to lo+sg/g, which is 4 to 10 times higher than that of the nutrient-deficient culture. The obtained algae is treated in the same manner as conventional algae treatment and used as is as algae containing high astaxanthin content, or astaxanthin is extracted from the algae and used.

〔発明の効果〕〔Effect of the invention〕

以上の通り、本発明によれば、アスタキサンチンを生合
成する緑藻類を特定の塩類を含む培地で培養するように
したので、簡単な培養法により。
As described above, according to the present invention, green algae that biosynthesize astaxanthin are cultured in a medium containing specific salts, so that a simple culture method can be used.

高濃度にアスタキサンチンを含有する緑藻類を生産する
ことができる。
Green algae containing astaxanthin at high concentrations can be produced.

〔実施例〕〔Example〕

以下、本発明の実施例について説明する。 Examples of the present invention will be described below.

実施例1 セネデスムス・クロレロイズ(Scanedesmus
chlorelloidas)を通常の培養液を用いて
、2I2容量の扁平フラスコにより予備培養した。培地
組成は表2の通りであり、培養条件は温度28℃、蛍光
燈による連続照明(約15000Lux)、3容量%の
炭酸ガスを含む空気によってバブリングを行った。培養
開始濃度はPCV(lQ中の生細胞量) 3 cc前後
であったが、6日間培養後PCV 32ccとなった。
Example 1 Scenedesmus chlorellois
chlorelloidas) was precultured in a 2I2 capacity flat flask using a normal culture medium. The medium composition was as shown in Table 2, and the culture conditions were a temperature of 28° C., continuous illumination with a fluorescent light (approximately 15,000 Lux), and bubbling with air containing 3% by volume of carbon dioxide gas. The starting concentration of the culture was around 3 cc of PCV (amount of living cells in 1Q), but after 6 days of culture, the PCV was 32 cc.

ついで遠心分離によりセネデスムスを収穫し、一部を乾
燥してアスタキサンチンの含有量を測定した。残りを2
分し、一方をN欠乏培養(表2の組成よりKNO,を除
いたもの)、もう一方を本発明によるナトリウム塩培地
(表2の組成にNaCQo、5M[約3重量%濃度]を
加えたもの)によって4〜6日間培養した。培養開始時
の濃度はPCV 14ccであった。培養温度、照明、
炭酸ガス濃度等は予備培養と同様である。培養を続ける
ことによって、いずれも培養液は赤色を示し、セネデス
ムスがアスタキサンチンを生合成していくのが確認され
た。
Scenedesmus was then harvested by centrifugation, a portion was dried, and the astaxanthin content was measured. 2 remaining
One part was cultured with N deficiency (KNO was removed from the composition in Table 2), and the other was a sodium salt medium according to the present invention (NaCQo, 5M [approximately 3% by weight concentration] was added to the composition in Table 2). cultured for 4 to 6 days. The concentration at the start of culture was 14 cc of PCV. Culture temperature, lighting,
Carbon dioxide concentration, etc. are the same as in the preliminary culture. As the culture continued, the culture solution in both cases turned red, confirming that Scenedesmus was biosynthesizing astaxanthin.

培養終了時のセネデスムスの濃度、およびアスタキサン
チンの含有量は表3のとおりであり、本発明によってア
スタキサンチンの含有量はN欠乏培養と比べて、大なる
ものであった。
The concentration of Scenedesmus and the content of astaxanthin at the end of the culture are shown in Table 3, and the content of astaxanthin according to the present invention was greater than that in the N-deficient culture.

表2 培地組成 表3 アスタキサンチン含有量 Dv=乾燥重量 実施例2 クロレラ・ゾーフインゲンシX’ (Chlorall
azofingiensis)を表4の培養液で予備培
養し、遠心分離により収穫したのち2分し、一方をN欠
乏培養(表4より(NH,)、COを除いたもの)、も
う一方を本発明によるカリウム塩培養(表4にKl、G
 O,5M〔約3.7重量%濃度〕を加えたもの)とし
、グルコースを炭素源としてタンク(暗所)培養を行っ
た。温度は28℃、培養日数は4〜6日間であった。
Table 2 Medium Composition Table 3 Astaxanthin Content Dv = Dry Weight Example 2
azofingiensis) was precultured with the culture solution shown in Table 4, harvested by centrifugation, and then divided into two halves, one of which was cultured with N deficiency (from Table 4, (NH,), CO was removed), and the other was cultured according to the present invention. Potassium salt culture (Table 4 shows Kl, G
O.5M (approximately 3.7% by weight concentration) was added), and tank (dark) culture was performed using glucose as a carbon source. The temperature was 28°C, and the number of culture days was 4 to 6 days.

培養開始濃度はPCV 18cc、終了時のpcvは2
2〜26eeであった。
The concentration at the start of the culture was 18cc PCV, and the PCV at the end was 2.
It was 2-26ee.

それぞれの培養で得られたクロレラ中のアスタキサンチ
ンの含有量を表5に示した。
Table 5 shows the astaxanthin content in Chlorella obtained in each culture.

表4 培地 表5 アスタキサンチン含有量 代理人 弁理士 柳 原   成Table 4 Medium Table 5 Astaxanthin content Agent: Patent attorney Sei Yanagi Hara

Claims (2)

【特許請求の範囲】[Claims] (1)アスタキサンチンを生合成する緑藻類を、ナトリ
ウム塩、カリウム塩およびルビジウム塩から選ばれる1
種以上を0.2〜1M含む培地中で培養することを特徴
とするアスタキサンチン高含有緑藻類の生産方法。
(1) Green algae that biosynthesize astaxanthin are combined with 1 selected from sodium salt, potassium salt, and rubidium salt.
1. A method for producing green algae with a high content of astaxanthin, which comprises culturing the algae in a medium containing 0.2 to 1M of the above species.
(2)請求項1において、緑藻類がクラミドモナス、ヘ
マトコッカス、アンキストロデスムス、クロレラ、クロ
ロコックム、ケラストルム、クルシゲニア、ディクティ
オコッカス、セネデスムス、スコティエラまたはプロト
シフォンである方法。
(2) The method according to claim 1, wherein the green algae is Chlamydomonas, Haematococcus, Anchistrodesmus, Chlorella, Chlorococcus, Cerastrum, Cursigenia, Dictyococcus, Scenedesmus, Scotiera, or Protosiphon.
JP63012328A 1988-01-22 1988-01-22 Method for producing astaxanthin-rich green algae Expired - Fee Related JP2707572B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63012328A JP2707572B2 (en) 1988-01-22 1988-01-22 Method for producing astaxanthin-rich green algae

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63012328A JP2707572B2 (en) 1988-01-22 1988-01-22 Method for producing astaxanthin-rich green algae

Publications (2)

Publication Number Publication Date
JPH01187082A true JPH01187082A (en) 1989-07-26
JP2707572B2 JP2707572B2 (en) 1998-01-28

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* Cited by examiner, † Cited by third party
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