JPH0238197B2 - - Google Patents
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- Publication number
- JPH0238197B2 JPH0238197B2 JP58065213A JP6521383A JPH0238197B2 JP H0238197 B2 JPH0238197 B2 JP H0238197B2 JP 58065213 A JP58065213 A JP 58065213A JP 6521383 A JP6521383 A JP 6521383A JP H0238197 B2 JPH0238197 B2 JP H0238197B2
- Authority
- JP
- Japan
- Prior art keywords
- chlorella
- iodine
- culture
- medium
- ppm
- 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.)
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Description
本発明はヨウ素成分が淡水クロレラ細胞内に富
化固定化された高ヨウ素含有淡水クロレラの製造
方法に関するものである。クロレラ,セネデスム
ス,クロミドモナス等淡水性単細胞緑藻(以下単
にクロレラという)は通常の栽培植物に比べて増
殖速度や光の利用効率が極めて高く、かつタンパ
ク質,脂質,炭水化物,ビタミン,ミネラル等の
栄養素を多く含み、食糧や飼料として優れてい
る。また、それが含み生理活性物質は微生物や動
植物が成長を促進する作用があることが知られて
おり、さらにクロレラの医学的効果も注目されて
いる。クロレラは天然の海産性と工業的に淡水培
養された淡水性が有るが現在健康食品として多量
に製造販売されているのは淡水性であり、海産性
は生産性に問題があり工業化されるに至つていな
い。クロレラは消化器系潰瘍治療剤,高血圧治療
剤,コレステロール調整剤,抗ガン剤等としての
利用が期待され、そのための成分研究等が行なわ
れており、天然の海産クロレラと市販されている
淡水クロレラとでは薬効成分に微妙な相違があ
り、海産クロレラは有意と言われているものの未
だ原因が究明完成されるに至つていない。通常ク
ロレラには約7%程度のミネラル成分が含まれ、
その主なものは、リン,カリウム,マグネシウ
ム,カルシウム,イオウ,鉄,等などであり、こ
れらの成分が多く含まれていることは健康食品と
してあるいは医学的効果の面からクロレラの価値
を高める要因の1つとなつている。
本発明者らは、海産クロレラと淡水クロレラの
相違に着目し各種研究を行なつたところ、天然の
海産クロレラには、ヨウ素に換算して約80ppm程
度のヨウ素成分が含まれているものの、通常市販
されている淡水クロレラには認められうる程度の
ヨウ素成分は含まれていないことを見出し、さら
にはこの淡水クロレラをヨウ素イオン等を添加し
た培地で一定の条件下にて培養することにより海
産クロレラ以上の高ヨード含有クロレラが得ら
れ、その薬理効果も海産クロレラ以上であること
を見出し本発明を完成するに至つた。
一方、近年健康食品としていわゆるヨード卵が
注目されているように、ヨウ素成分はヨウ素成分
の不足による甲状線機能低下症等の治療に使用さ
れるばかりでなく、成長促進、高血圧やアレルギ
ー体質の改善、各種疾患の治療などに有効である
ことが認められるようになつており、ヨウ素成分
を高含量含むクロレラはクロレラ本来の特徴に加
えてヨウ素系成分による効果並びに他の成分との
併用効果が発揮されるものであり、ヨード卵以上
に利用価値の高いものである。ヨウ素イオン等は
殺菌剤として使用されている如く、淡水クロレラ
の増殖を阻害するものと予想されたが、試験結果
によるとその予想に反し比較的高濃度のヨウ素イ
オンを含む培地であつても淡水クロレラの増殖は
ほとんど阻害されないことを見出した。しかも、
ヨウ素イオンを含み培地で培養された淡水クロレ
ラは海産クロレラ以上に高い割合のヨウ素成分を
含み、しかもこのクロレラを充分洗浄してもヨウ
素成分の減少はほとんどないことにより、ヨウ素
原子はクロレラ細胞中である種の成分と結合する
形で固定されており、単にヨウ素イオンがクロレ
ラに吸収あるいは吸着された状態にあるものでは
ないことを確認した。
本発明は上記ヨウ素成分が富化されたクロレラ
の製造方法に関するものであり、即ち、ヨウ素イ
オン及び/又はヨウ素酸イオンを0.1ppm〜
800ppm含みPH4〜7の培地条件下光の存在下で
培養された淡水クロレラを乾燥することにより得
られるヨウ素含有量が100ppm以上であることを
特徴とする高ヨウ素含有淡水クロレラの製法であ
る。
海水には通常0.06ppm程度のヨウ素イオンを含
んでいる。この海水中で増殖した海産クロレラは
前記のようにヨウ素に換算して約80ppm程度のヨ
ウ素成分を含んでいる。一方、本発明によりヨウ
素に換算したヨウ素成分含有量が(乾燥重量当
り)100ppm以上の淡水クロレラが容易に得られ
る。本発明において得られるヨウ素成分が富化さ
れた淡水クロレラ中の乾燥重量当りのヨウ素成分
含有量のより好ましい範囲はヨウ素に換算して約
100〜2000ppmであるが、上限は必ずしもこの範
囲になくてはならないものではない。クロレラ中
のヨウ素成分含有量は通常培地中のヨウ素イオン
および/またはヨウ素酸イオン(以下両者をヨウ
素イオン等という)の濃度に左右され易い。即
ち、培地中のヨウ素イオン等の濃度が高い程クロ
レラ中のヨウ素成分含有量が高くなる。しかしな
がら、あまりに高い濃度のヨウ素イオン等を含む
培地ではクロレラの増殖が阻害され易くなる。従
つて、クロレラの種類にもよるが、培地中のヨウ
素イオン等の濃度は約0.5〜800ppmが適当であ
り、特に約1〜800ppmの範囲にあることが好ま
しい。
本発明において、好ましくはクロレラ・ピレノ
イドーサ、クロレラ・ブルガリス、クロレラ・エ
リプリイデアなどのクロレラが適当であるが、セ
ネデスムス、クラミドモナス、セレナストルム、
その他のクロレラであつてもよい。上記クロレラ
は通常淡水中で生育する淡水クロレラであるが、
その耐塩性変異種は海産クロレラと呼ばれてい
る。ヨウ素イオン等を含む培地は、クロレラ培養
培地に水溶性のヨウ化物やヨウ素酸塩等を添加す
ることにより容易に得られる。たとえばヨウ化カ
リウム、ヨウ化ナトリウム、ヨウ化カルシウムそ
の他の無機ヨウ化物やヨウ化水素などのヨウ素イ
オン源、ヨウ素酸カリウム、ヨウ素酸ナトリウ
ム、ヨウ素酸カルシウム、その他のヨウ素酸塩や
ヨウ素酸塩などのヨウ素酸イオン源を使用し得
る。また、ヨウ素イオン等を含む地下かん水など
に下記炭素源等の栄養源を添加して培地を製造す
ることもできる。培地におけるヨウ素イオン等の
濃度はヨウ素の培養の全範囲において前記濃度範
囲に保つことが好ましいが、必ずしもこれに限ら
れるものではない。特にヨウ素イオン等を含まな
い培地である程度ヨウ素の培養を行なつた後培地
にヨウ素イオン等のイオン源であるヨウ化物など
を添加して培養を続ける方法の採用が好ましい。
また、ヨウ素イオン等の濃度が培養の途中でヨウ
素への取り込みが進むことなどの理由により
0.5ppm以下となるような場合があつてもよい。
しかしながら、種となるヨウ素を添加した培地に
おいてヨウ素イオン等の濃度を常に0.1ppm以上、
好ましくは0.5〜800ppmに保ちながら培養を行な
う方法が最も好ましい。このために、培養の途中
で連続的にあるいは断続的に培地にイオン源を追
加する方法の採用が好ましい。また、イオン源の
追加は1回限りであつてもよく、イオン源を追加
することとなく上記濃度に保つことも勿論可能で
ある。いずれの場合であつても、ヨウ素イオン等
の存在する培地でのヨウ素の培養は少なくとも1
日、特に少なくとも数日間であることが好まし
い。
ヨウ素培養地は、上記ヨウ素イオン等の存在を
除いて通常のヨウ素培養培地を使用しうる。通常
のヨウ素培養培地は下記炭素源、窒素源、無機
源、その他を含む淡水であるが前記のような場合
により海水などの塩水やかん水であつてもよい。
炭素源としては、炭酸ガス;酢酸、クエン酸、コ
ハク酸その他の有機酸やそれらの塩;グルコー
ル、シユークロス、ガラクトース、その他の糖
類;エタノール、アミノ酸、ペプチド、その他の
有機物などが使用できる。窒素源としては、アン
モニウム塩、硝酸塩、アンモニア、尿素、アミノ
酸などが使用できる。無機源としてはリン、イオ
ウ、カリウム、マグネシウム、鉄、マンガン、コ
バルト、モリブデン、亜鉛、銅などの化合物があ
る。さらに他の栄養源や成長促進剤、たとえば酵
母エキス、糖密、ホルモンなどを使用することも
できる。これらの成分は、ヨウ素イオン等のイオ
ン源として使用される化合物に含まれていてもよ
い。たとえば、カリウムを必要とする場合、ヨウ
化カリウムをカリウム源とすることもできる。現
在企業的なヨウ素の培養においては、炭素源とし
て酢酸などの有機化合物が炭酸ガスとともに使用
されている。しかし、炭酸ガスのみを炭素源とす
る培養も知られている。本発明においては、酢酸
などの有機酸やそれらの塩、あるいは糖類を好ま
しくは炭酸ガスと併用して炭酸源とすることが好
ましいが、炭酸ガスのみを炭素源としてもよい。
培地における炭素源の濃度は、炭素ガスを除いて
0.1〜10重量%程度が適当である。窒素源は無機
源ともに特に多くは必要とせず、それぞれ通常1
重量%以下に充分であるが、これに限られるもの
ではない。
培地において特に炭素源はほぼ一定濃度に保た
れることが好ましい。たとえば、酢酸に例をとれ
ば、培地中の酢酸濃度は培養の期間中5±3重量
%に維持されることが好ましい。この場合酢酸は
炭素源であるとともに培地のPH調節剤としても利
用しうるからである。培地のPH調節は雑菌等の増
殖を抑制する面で重要である。
通常PH4〜7でクロレラの培養が可能であるが
アルカリ性であると雑菌が増殖し易い。
好ましいPHは約4.5〜6が適当である。酢酸を
炭素源とする場合、上記酢酸濃度でこのPHの範囲
を維持することができる。また、補助的に、さら
には酢酸を使用しない場合では、他の酸類でPHの
調節を行なうことができる。
培養終了後、遠心分離等によりクロレラと水分
との分離が行なわれ、同時に水洗などにより洗浄
が行なわれて水分含有量の少ないクロレラを得
る。このクロレラは続いてスプレードライや凍結
乾燥法などの方法で乾燥されて製品とされる。乾
燥はクロレラの変質を防ぐ面で重要であり、現在
のところスプレードライ法が最も好ましいとさ
れ、凍結乾燥法は酵素の活性が維持されているの
で製品変質を招き易い問題といわれている。しか
し、クロレラそのものは勿論クロレラ中の生理活
性物質などの成分を抽出して利用する場合などで
は、凍結乾燥法が成分の変質を起さずに成分抽出
を行なうことができるのでより好ましいと考えら
れる。
以下に本発明を実施例により具体的に説明する
が、本発明はこの実施例に限られるものではな
い。
実施例 1
下記第1表記載の組成の培養液を使用して、ク
ロレラ・ピレノイドーサおよびクロレラ・エリプ
リイデアの培養を行なつた。
第 1 表
水道水 20
酢 酸 1Kg
KNO3 5g
KH2PO4 5g
MgSO4・7H2O 10g
くえん酸鉄 0.04g
MnCl2 0.02g
60の培養槽に上記培養液40を加え、クロレ
ラ種株約5g(乾燥重量換算)を加え、室温にて
エアレーシヨンを行ないながら500〜20000ルツク
スの光照射度下で培養を行なつた。培養液のPHを
測定し、培養期間中PHが上昇すると酢酸を加える
ことをくり返して、培養液のPHを常に4.5〜6.5の
範囲に保つた。培養開始10日後にヨウ化カリウム
を0.8g培養液に加え、さらに培養開始13日後に
0.8gを培養液に加えた。培養開始20日後に収穫
し、遠心分離により藻体を分離し、充分に水洗
し、凍結乾燥した。収量は約15gであつた。
得られた乾燥クロレラ中に含まれるヨウ素分を
螢光x線分析装置で分析したところ、約100ppm
のヨウ素分が含まれていた。一方、培養液にヨウ
化カリウムを加えることなく上記と同じ方法で培
養したクロレラについてヨウ素分を分析したとこ
ろ、ヨウ素分は含まれていないことが確認され
た。
実施例 2
ppm電極と培地補給用チユーブ及び培養液サン
プリングチユーブを取り付けた1のエルレンマ
イヤーフラスコに第2表に示したクロレラ培養用
の基本培地を500ml1分注し、120℃、15分間の条
件で滅菌処理を行ない、次に無菌条件下でミリポ
アフイルター(HA0.45μm)を通じて調整したヨ
ウ化カリウム溶液をヨウ素イオン濃度として0,
100,300,500,800ppmになるように培地に添加
した。次に表2に示した培地で5%の炭酸ガスを
含む空気を通気しながら光照射10Klux30℃で培
地を行なつたクロレラピレノイドサ(Chlorella
pyrenoidosa C―28)の50mlを上記において調
整した1のエレンマイヤーフラスコに植え、光
照射10Klux,30℃で培養液中のPH6.5〜7.0の範囲
になるようにPHコントローラにより第3表に示す
補給培地(PH3.5)を自動的に添加しながら振盪
培養を行なつた。
その経時的なクロレラの増殖と藻体内に取り込
まれたヨウ素量について示したのが第1図〜第5
図である。クロレラの増殖はヨウ素を含まないI-
=0ppmのコントロールが一番良いが、培地中の
ヨウ素が100〜800ppmの範囲ではクロレラの増殖
速度、藻体収量ともにほとんど同等であつた。し
かしヨウ素取込み量はクロレラの増殖に伴ない増
加し、かつ培地のヨウ素濃度が高いなど取込みヨ
ウ素量が多いという結果が得られた。
なお、ヨウ素測定は経時的に採取したクロレラ
を遠心分離により十分洗浄し、凍結乾燥により乾
燥させたクロレラをクロム酸―塩素酸―過塩素酸
の混液による酸化分解を行ない、その分解液をチ
オシアン酸鉄()―ヨウ素接触反応法によりヨ
ウ素の取込量の測定を行なつた。
The present invention relates to a method for producing high-iodine-containing freshwater chlorella in which iodine components are enriched and immobilized within freshwater chlorella cells. Freshwater unicellular green algae (hereinafter simply referred to as chlorella), such as Chlorella, Scenedesmus, and Chromydomonas, have extremely high growth rates and light utilization efficiency compared to conventionally cultivated plants, and are rich in nutrients such as proteins, lipids, carbohydrates, vitamins, and minerals. It is excellent as food and feed. In addition, the physiologically active substances it contains are known to have the effect of promoting the growth of microorganisms, animals and plants, and the medical effects of chlorella are also attracting attention. There are two types of chlorella: natural marine-produced chlorella and industrially cultivated freshwater-produced chlorella, but the freshwater version is currently produced and sold in large quantities as a health food, while the marine-produced version has problems with productivity and has not been industrialized. I haven't reached it yet. Chlorella is expected to be used as a gastrointestinal ulcer treatment, high blood pressure treatment, cholesterol regulator, anti-cancer agent, etc., and research on its ingredients is being carried out. Natural marine chlorella and commercially available freshwater chlorella There are subtle differences in the medicinal ingredients between the two, and although marine chlorella is said to be significant, the cause has not yet been fully investigated. Normally, chlorella contains about 7% mineral components.
The main components are phosphorus, potassium, magnesium, calcium, sulfur, iron, etc. The high content of these components is a factor that increases the value of chlorella as a health food and in terms of medical effects. It has become one of the The present inventors conducted various studies focusing on the differences between marine chlorella and freshwater chlorella, and found that although natural marine chlorella contains approximately 80 ppm of iodine in terms of iodine, It was discovered that commercially available freshwater chlorella does not contain appreciable amounts of iodine, and furthermore, by culturing this freshwater chlorella under certain conditions in a medium containing iodine ions, etc., marine chlorella was cultivated. The above-mentioned high iodine-containing chlorella was obtained, and the present inventors discovered that its pharmacological effects were even greater than that of marine chlorella, leading to the completion of the present invention. On the other hand, as the so-called iodine eggs have been attracting attention as a health food in recent years, iodine components are not only used to treat hypothyroidism caused by a lack of iodine components, but also to promote growth, improve high blood pressure and allergic predisposition. Chlorella, which contains a high content of iodine, has been recognized to be effective in the treatment of various diseases, and in addition to the original characteristics of chlorella, iodine-based ingredients also exhibit effects as well as effects when used in combination with other ingredients. It has a higher utility value than iodine eggs. It was expected that iodine ions would inhibit the growth of freshwater chlorella, as they are used as disinfectants, but test results showed that contrary to that expectation, even in a medium containing a relatively high concentration of iodine ions, freshwater chlorella It was found that the growth of Chlorella was hardly inhibited. Moreover,
Freshwater chlorella cultured in a medium containing iodine ions contains a higher proportion of iodine than marine chlorella, and even if this chlorella is thoroughly washed, there is almost no decrease in iodine, meaning that iodine atoms are not present in chlorella cells. It was confirmed that iodine ions are fixed in a form that binds to certain components, and that iodine ions are not simply absorbed or adsorbed by chlorella. The present invention relates to a method for producing chlorella enriched with the above iodine component, that is, iodine ions and/or iodate ions are added to 0.1 ppm to
This is a method for producing high-iodine-containing freshwater chlorella, characterized in that the iodine content is 100 ppm or more, obtained by drying freshwater chlorella containing 800 ppm and cultured in the presence of light under a medium condition of pH 4 to 7. Seawater normally contains about 0.06 ppm of iodine ions. As mentioned above, marine chlorella grown in seawater contains about 80 ppm of iodine. On the other hand, according to the present invention, freshwater chlorella having an iodine component content (per dry weight) of 100 ppm or more in terms of iodine can be easily obtained. A more preferable range of the iodine content per dry weight of the iodine-enriched freshwater chlorella obtained in the present invention is approximately
100 to 2000 ppm, but the upper limit does not necessarily have to be within this range. The iodine component content in chlorella is usually easily influenced by the concentration of iodine ions and/or iodate ions (hereinafter both referred to as iodine ions, etc.) in the culture medium. That is, the higher the concentration of iodine ions, etc. in the medium, the higher the iodine component content in chlorella. However, in a medium containing too high a concentration of iodine ions, etc., the growth of chlorella is likely to be inhibited. Therefore, although it depends on the type of Chlorella, the appropriate concentration of iodine ions, etc. in the medium is about 0.5 to 800 ppm, particularly preferably in the range of about 1 to 800 ppm. In the present invention, Chlorella such as Chlorella pyrenoidosa, Chlorella vulgaris, and Chlorella elliplyidea are preferably suitable; however, Chlorella such as Scenedesmus, Chlamydomonas, Selenastrum,
Other chlorella may also be used. The above chlorella is a freshwater chlorella that usually grows in fresh water.
The salt-tolerant variant is called marine chlorella. A medium containing iodine ions and the like can be easily obtained by adding water-soluble iodide, iodate, etc. to a chlorella culture medium. For example, potassium iodide, sodium iodide, calcium iodide and other inorganic iodides, iodine ion sources such as hydrogen iodide, potassium iodate, sodium iodate, calcium iodate, and other iodates and iodates. An iodate ion source may be used. Further, a culture medium can also be produced by adding a nutrient source such as the carbon source described below to underground brine containing iodine ions or the like. The concentration of iodine ions, etc. in the culture medium is preferably maintained within the above concentration range throughout the entire range of iodine culture, but is not necessarily limited to this. In particular, it is preferable to adopt a method in which iodine is cultured to some extent in a medium that does not contain iodine ions, etc., and then iodide, which is an ion source such as iodine ions, is added to the medium and the culture is continued.
In addition, due to reasons such as the concentration of iodine ions, etc. increasing incorporation into iodine during the culture,
There may be cases where the concentration is 0.5 ppm or less.
However, in the medium containing iodine as a seed, the concentration of iodine ions, etc. should always be 0.1 ppm or more.
The most preferred method is to carry out culturing while maintaining the concentration preferably from 0.5 to 800 ppm. For this reason, it is preferable to adopt a method of adding an ion source to the culture medium continuously or intermittently during the culture. Further, the ion source may be added only once, and it is of course possible to maintain the above concentration without adding an ion source. In any case, the iodine culture in a medium containing iodine ions, etc. is carried out for at least 1 hour.
Preferably, the duration is 1 day, especially at least several days. As the iodine culture medium, a normal iodine culture medium can be used except for the presence of the above-mentioned iodine ions. The usual iodine culture medium is fresh water containing the following carbon sources, nitrogen sources, inorganic sources, and others, but depending on the above-mentioned circumstances, salt water such as seawater or brine may be used.
As the carbon source, carbon dioxide gas; acetic acid, citric acid, succinic acid, and other organic acids and their salts; glycol, sucrose, galactose, and other sugars; ethanol, amino acids, peptides, and other organic substances can be used. As the nitrogen source, ammonium salts, nitrates, ammonia, urea, amino acids, etc. can be used. Inorganic sources include compounds such as phosphorus, sulfur, potassium, magnesium, iron, manganese, cobalt, molybdenum, zinc, and copper. Additionally, other nutritional sources and growth promoters may be used, such as yeast extract, molasses, hormones, etc. These components may be included in the compound used as an ion source such as iodine ions. For example, if potassium is required, potassium iodide can be used as a potassium source. Currently, in commercial iodine cultivation, organic compounds such as acetic acid are used as carbon sources along with carbon dioxide gas. However, cultivation using only carbon dioxide gas as a carbon source is also known. In the present invention, an organic acid such as acetic acid, a salt thereof, or a saccharide is preferably used in combination with carbon dioxide gas as the carbon source, but carbon dioxide gas alone may be used as the carbon source.
The concentration of carbon sources in the culture medium, excluding carbon gas, is
Approximately 0.1 to 10% by weight is appropriate. Neither the inorganic sources nor the nitrogen sources are required in particularly large amounts; each is usually 1
% by weight or less, but is not limited thereto. It is preferable that the carbon source in particular be kept at a substantially constant concentration in the culture medium. For example, taking acetic acid as an example, the acetic acid concentration in the medium is preferably maintained at 5±3% by weight during the culture period. This is because acetic acid in this case can be used not only as a carbon source but also as a PH regulator of the medium. Adjusting the pH of the culture medium is important in suppressing the growth of various bacteria. Normally, chlorella can be cultured at a pH of 4 to 7, but if the pH is alkaline, bacteria can easily grow. The preferred pH is approximately 4.5 to 6. When acetic acid is used as a carbon source, this PH range can be maintained at the above acetic acid concentration. Furthermore, when acetic acid is not used, the pH can be adjusted with other acids. After the cultivation is completed, chlorella and water are separated by centrifugation or the like, and at the same time, washing is performed by washing with water to obtain chlorella with a low water content. This chlorella is then dried into products using methods such as spray drying and freeze drying. Drying is important in preventing deterioration of Chlorella, and currently the spray drying method is said to be the most preferred method, while the freeze drying method is said to be more likely to cause product deterioration because the enzyme activity is maintained. However, when extracting and utilizing not only Chlorella itself but also components such as physiologically active substances in Chlorella, the freeze-drying method is considered more preferable because it can extract components without causing deterioration of the components. . EXAMPLES The present invention will be specifically explained below using Examples, but the present invention is not limited to these Examples. Example 1 Chlorella pyrenoidosa and Chlorella ellipridea were cultured using a culture solution having the composition shown in Table 1 below. Table 1 Tap water 20 Acetic acid 1Kg KNO 3 5g KH 2 PO 4 5g MgSO 4・7H 2 O 10g Iron citrate 0.04g MnCl 2 0.02g Add the above culture solution 40 to a 60-liter culture tank, and add about 5g of Chlorella seed stock. (in terms of dry weight) and cultured under a light irradiation intensity of 500 to 20,000 lux while performing aeration at room temperature. The PH of the culture solution was measured, and when the PH increased during the culture period, acetic acid was repeatedly added to keep the PH of the culture solution in the range of 4.5 to 6.5. 0.8g of potassium iodide was added to the culture solution 10 days after the start of culture, and then 13 days after the start of culture.
0.8g was added to the culture solution. The algae were harvested 20 days after the start of culture, and the algal bodies were separated by centrifugation, thoroughly washed with water, and freeze-dried. The yield was about 15g. When the iodine content in the dried chlorella obtained was analyzed using a fluorescent x-ray analyzer, it was found to be approximately 100 ppm.
It contained iodine. On the other hand, when the iodine content of Chlorella cultured in the same manner as above without adding potassium iodide to the culture solution was analyzed, it was confirmed that it did not contain iodine. Example 2 One 500 ml portion of the basic medium for chlorella culture shown in Table 2 was poured into Erlenmeyer flask 1 equipped with a ppm electrode, a medium supply tube, and a culture solution sampling tube, and the conditions were maintained at 120°C for 15 minutes. After sterilizing with
It was added to the medium at concentrations of 100, 300, 500, and 800 ppm. Next, the culture medium shown in Table 2 was cultured at 10Klux and 30°C with light irradiation while aerating air containing 5% carbon dioxide gas.
pyrenoidosa C-28) was planted in the Ellenmeyer flask (1) adjusted above, and irradiated with light at 10 Klux at 30°C, using a PH controller to maintain the pH in the culture medium in the range of 6.5 to 7.0 as shown in Table 3. Shaking culture was performed while automatically adding supplementary medium (PH3.5). Figures 1 to 5 show the growth of Chlorella over time and the amount of iodine taken into the algae.
It is a diagram. Chlorella growth does not contain iodine I -
= 0 ppm is the best control, but when the iodine in the medium was in the range of 100 to 800 ppm, both the growth rate of Chlorella and the yield of algae were almost the same. However, the amount of iodine uptake increased as Chlorella multiplied, and the iodine concentration in the medium was high, resulting in a large amount of iodine uptake. In addition, for iodine measurement, chlorella collected over time was thoroughly washed by centrifugation, and the chlorella dried by freeze-drying was subjected to oxidative decomposition using a mixture of chromic acid, chloric acid, and perchloric acid, and the decomposed liquid was treated with thiocyanic acid. The amount of iodine uptake was measured using the iron()-iodine contact reaction method.
【表】【table】
【表】
薬効薬理試験
抗腫瘍効果(Sarcoma―180固形ガンに対する
果)
(方法)
Sarcoma―180 1×106個をICRマウス(5週
齢雄性)に皮下移植し、翌日から本発明により得
られた淡水クロレラ凍結乾燥物5g/Kgをえさに
混入して4連投の後再度4日目より5連投を行な
う。移植後21日目に腫瘍重量を測定して効果を測
定した。[Table] Drug efficacy pharmacology test Antitumor effect (effect on Sarcoma-180 solid cancer) (Method) 6 Sarcoma-180 1×10 cells were subcutaneously transplanted into ICR mice (5-week-old male), and from the next day, the results were obtained according to the present invention. 5 g/Kg of freeze-dried freshwater chlorella was mixed into the feed, and after 4 consecutive feedings, 5 consecutive feedings were repeated from the 4th day. Tumor weight was measured on the 21st day after transplantation to determine the effect.
【表】
クロレラ投与
(結果)
以下表4に示すように、本発明により得られた
クロレラは約37%の抗腫瘍効果を示した。これに
反し、一般の淡水クロレラは腫瘍の成長を促進
し、海産クロレラはやや腫瘍の成長を抑制した。[Table] Chlorella Administration (Results) As shown in Table 4 below, the chlorella obtained according to the present invention showed an antitumor effect of about 37%. On the other hand, common freshwater chlorella promoted tumor growth, and marine chlorella slightly inhibited tumor growth.
【表】【table】
第1図〜第5図はクロレラ培養時間に対するク
ロレラの増殖量(PCV)と増殖したクロレラ中
のヨウ素の取込量を示すグラフであり、第1図は
培養液中のヨウ素イオン量[-]が0の場合、
第2図は100ppmの場合、第3図は300ppmの場
合、第4図は500ppmの場合、および第5図は
800ppmの場合を示す。
Figures 1 to 5 are graphs showing the amount of chlorella proliferation (PCV) and the amount of iodine taken up in the grown chlorella against the culture time, and Figure 1 shows the amount of iodine ions in the culture solution [ - ] If is 0,
Figure 2 shows the case of 100ppm, Figure 3 shows the case of 300ppm, Figure 4 shows the case of 500ppm, and Figure 5 shows the case of 500ppm.
The case of 800ppm is shown.
Claims (1)
0.1ppm〜800ppm含みPH4〜7の培地条件下光の
存在下で培養された淡水クロレラを乾燥すること
により得られるヨウ素含有量が100ppm以上であ
ることを特徴とする高ヨウ素含有淡水クロレラの
製法。1 Iodine ion and/or iodate ion
A method for producing high-iodine-containing freshwater chlorella, which is obtained by drying freshwater chlorella containing 0.1 to 800 ppm and cultured in the presence of light under a medium pH of 4 to 7.The iodine content is 100 ppm or more.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6521383A JPS59192083A (en) | 1983-04-15 | 1983-04-15 | Preparation of unicellular green alga |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6521383A JPS59192083A (en) | 1983-04-15 | 1983-04-15 | Preparation of unicellular green alga |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61162144A Division JPS62123128A (en) | 1986-07-11 | 1986-07-11 | Fresh water chlorella containing iodine and anti-cancer drug comprising same as main component |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59192083A JPS59192083A (en) | 1984-10-31 |
| JPH0238197B2 true JPH0238197B2 (en) | 1990-08-29 |
Family
ID=13280406
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6521383A Granted JPS59192083A (en) | 1983-04-15 | 1983-04-15 | Preparation of unicellular green alga |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59192083A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH082294B2 (en) * | 1988-09-20 | 1996-01-17 | 文生 大貫 | Culture medium of Chlamydomonas single-cell green algae Earl sager strain 95 |
| CN104823898B (en) * | 2015-06-09 | 2017-06-06 | 广东海洋大学 | The preparation method and its feeding method of a kind of Duo Lin Xi prelarva open-mouthed baits |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5714831A (en) * | 1980-07-01 | 1982-01-26 | West Electric Co Ltd | Electronic flash device |
-
1983
- 1983-04-15 JP JP6521383A patent/JPS59192083A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59192083A (en) | 1984-10-31 |
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