JPS633577B2 - - Google Patents
Info
- Publication number
- JPS633577B2 JPS633577B2 JP58151848A JP15184883A JPS633577B2 JP S633577 B2 JPS633577 B2 JP S633577B2 JP 58151848 A JP58151848 A JP 58151848A JP 15184883 A JP15184883 A JP 15184883A JP S633577 B2 JPS633577 B2 JP S633577B2
- Authority
- JP
- Japan
- Prior art keywords
- mycelium
- culture
- medium
- glucose
- wheat germ
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000007788 liquid Substances 0.000 claims description 15
- 241000209140 Triticum Species 0.000 claims description 12
- 235000021307 Triticum Nutrition 0.000 claims description 12
- 240000007235 Cyanthillium patulum Species 0.000 claims description 11
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 11
- 239000008103 glucose Substances 0.000 claims description 11
- 235000013402 health food Nutrition 0.000 claims description 9
- 238000012258 culturing Methods 0.000 claims description 3
- 239000002609 medium Substances 0.000 description 20
- 239000000306 component Substances 0.000 description 11
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 9
- 244000223760 Cinnamomum zeylanicum Species 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 235000017803 cinnamon Nutrition 0.000 description 6
- 239000001965 potato dextrose agar Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000011218 seed culture Methods 0.000 description 3
- 239000004575 stone Substances 0.000 description 3
- 241000221198 Basidiomycota Species 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- 239000012533 medium component Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000222336 Ganoderma Species 0.000 description 1
- 241000336458 Ligusticum lucidum Species 0.000 description 1
- 240000007163 Livistona chinensis Species 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 239000001888 Peptone Substances 0.000 description 1
- 108010080698 Peptones Proteins 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 241000205407 Polygonum Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 230000001093 anti-cancer Effects 0.000 description 1
- 230000001315 anti-hyperlipaemic effect Effects 0.000 description 1
- 230000003276 anti-hypertensive effect Effects 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229940041514 candida albicans extract Drugs 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- WORJEOGGNQDSOE-UHFFFAOYSA-N chloroform;methanol Chemical compound OC.ClC(Cl)Cl WORJEOGGNQDSOE-UHFFFAOYSA-N 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 241000411851 herbal medicine Species 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000009630 liquid culture Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 230000001256 tonic effect Effects 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 238000003809 water extraction Methods 0.000 description 1
- 239000012138 yeast extract Substances 0.000 description 1
Landscapes
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Non-Alcoholic Beverages (AREA)
- Medicines Containing Plant Substances (AREA)
Description
本発明はマンネンタケ培養菌糸体からなる健康
食品に関する。
マンネンタケはヒダナシタケ目サルノコシカケ
科に属する担子菌で、霊芝ともいわれ、古くから
中国においてすぐれた生薬として珍重されてい
る。近年、我国においても、マンネンタケの有効
成分を科学的に解明する研究がさかんに行なわれ
るようになり、その制ガン作用、抗高血圧作用、
抗高脂血症作用等が次第に明らかにされつつあ
り、有効成分を単離して医薬として用いたり、マ
ンネンタケそのものをいわゆる健康食品等として
用いるなどの試みが種々なされている。
しかしながら、元来、マンネンタケは中国でも
天然に極く希にしか生育せず、入手が著しく困難
で非常に高価なものである。最近、我国において
は、マンネンタケの人工栽培が可能となり、入手
が比較的容易となつたものの、依然として高価で
あり、しかも、生育に2〜5年の長期間を必要と
する。そのうえ、人工栽培で得られるマンネンタ
ケには天然のものと比較して含有成分が異なつて
いるものが多いという問題がある。
このような事情にかんがみ、本発明者らは容易
に、かつ、安価に、しかも、天然のものと同等も
しくは近似した含有成分を有するマンネンタケを
得るべく鋭意研究を重ねる間に、意外にも、特定
の組成を有する液体培地がマンネンタケの菌糸体
培養に極めて有効であり、短期間で収率よく、安
価に、天然のマンネンタケ含有成分に近似した成
分を含有するマンネンタケ菌糸体が得られ、これ
が健康食品として好適であることを見出した。前
記のごとく、マンネンタケの人工栽培がすでに行
なわれているが、これはマンネンタケ子実体の栽
培であり、本発明のごとく、マンネンタケの菌糸
体を効率よく液体培養して天然の子実体に近似し
た成分を有する菌糸体を得た例は従来見当らな
い。
かくして、本発明は特定の組成の液体培地中で
液体培養して得られる、天然の子実体に近似した
成分を含有する菌糸体からなる新規マンネンタケ
培養菌糸体健康食品を提供するものである。本発
明によれば、グルコース0.2〜10w/v%および
小麦胚芽0.2〜2w/v%を必須成分とすることに
より、短期間で、安価に収率よく、天然のマンネ
ンタケ菌糸体が得られ、培養終了後、培養物から
菌糸体を分離し、これをそのまま通常のキノコ類
と同様に、あるいは、常法に従つて公知の形態の
健康食品とすることができ、これは、天然のマン
ネンタケ子実体を用いた健康食品と同等に使用す
ることができる。
すなわち、本発明のマンネンタケ菌糸体を得る
には、まず、マンネンタケ種菌糸を、グルコース
および小麦胚芽を必須成分とする液体培地中で液
体培養する。
該培地成分として用いるグルコースおよび小麦
胚芽は培地成分として通常入手しうるものであれ
ばいずれでもよい。グルコースは培地全量に基い
て0.2〜10w/v%、好ましくは1〜8w/v%の
割合で用いる。グルコースの量が0.2w/v%よ
り低くても、また、10w/v%を超えても菌糸体
の収量が低下する。小麦胚芽は培地全量に基いて
0.2〜2w/v%、好ましくは、0.5〜1.0w/v%の
割合で用いる。小麦胚芽の量も0.2w/v%より
低いと菌糸体の収量が低下し、また、2w/v%
を超えると経済的に不利となる。ことに、本発明
においては、該液体培地中の小麦胚芽:グルコー
スの重量比を1:1〜8とすることが好ましく、
これにより、マンネンタケ菌糸体の収率が向上す
る。
所望により、該液体培地には、リン、マンガ
ン、マグネシウム、カルシウム、鉄などの塩類の
ごときミネラル成分や、他の穀類胚芽、米ぬか、
コーン・ステイープ・リカー、ビタミン類、核酸
類、アミノ酸類、殿粉、酵母エキス、ペプトンな
どのごとき他の栄養成分を適宜添加してもよい。
該液体培地は常法に従つて調製することがで
き、例えば、所定の各成分を滅菌水に添加し、分
散、溶解させる。得られた培地は、通常、120〜
130℃で、15〜30分間滅菌処理した後、マンネン
タケ菌糸体の培養に用いられる。
マンネンタケ菌糸体の培養は、該液体培地に適
当量の種菌糸を接種し、好気的条件下に行なわれ
る。
用いる種菌糸は担子菌類に属するヒダナシタケ
目サルノコシカケ科マンネンタケのものであれば
いずれでもよく、例えば、(株)河村式椎葺研究所
(静岡県藤枝市青葉町1―1―11)より入手でき
る。
通常、種菌糸の接種量は約5〜10mg/100ml培
地で充分であり、200〜300r.p.m.の撹拌下、温度
25〜30℃、通気量0.5〜3.0v.v.m.で7〜21日間暗
所において培養を行なうことにより、天然のマン
ネンタケ子実体の含有成分に近似した成分を有す
るマンネンタケ菌糸体が高収率で得られる(例え
ば、この培養によれば、従来のマンネンタケ人工
栽培用の種菌培養に用いられるポテト・デキスト
ロース・ブロス(PDB)培地と比べて9〜50倍
もの菌糸体収量を達成することができる)。
培養終了後、得られた培養物から菌糸体を分離
する。この分離は、過、遠心分離などの常法に
従つて行なうことができる。なお、菌糸体を分離
した残りの培養液中にも有用な成分が蓄積されて
いるので、それも濃縮乾固等により加工して菌糸
体と同様に使用できる。
かくして得られた菌糸体は、一般に、径1〜5
mmの球状を呈しており、キノコ独特の歯ざわりと
風味を有し、また、小麦胚芽の香ばしい風味を有
しており、これはそのまま健康食品として用いる
ことができ、通常の調理法によつて、例えば、ス
ープ、佃煮などとすることができる。また、常法
に従つて乾燥し、要すれば粉砕し、食品に許容さ
れる担体と合して粉剤、錠剤、丸剤、顆粒剤、カ
プセル剤などとすることもでき、また、種々の食
品の滋養、強壮成分として用いることもできる。
添付の第1図および第2図に、本発明で得られ
たマンネンタケ培養菌糸体(後記実施例2)を熱
水抽出し、さらに酢酸エチルで抽出した抽出物の
ガスクロマトグラムおよび薄層クロマトグラムを
示す。各クロマトグラフイーの条件はつぎのとお
りである。
ガスクロマトグラフイー
使用機種:島津製作所製GC―7A;カラム2%
OV―1、ユニポートHP(60〜80メツシユ)、3
mm×200cm;カラム温度:150℃で8分間保持、つ
いで、80分で230℃まで上昇;気化室温度:280
℃;検出器:F1D。なお、試料は常法に従つて
TMS化した。
薄層クロマトグラフイー
プレート:メルク社製シリカゲル;展開溶媒:
クロロホルム―メタノール(9:1):発色:I2
およ也び紫外線(第2図中、点線で示すスポツト
はI2で発色、実線で示すスポツトは紫外線ランプ
下で発色し、かつ、I2で強く発色)。
第1図および第2図中、クロマトグラムAは天
然のマンネンタケ子実体の熱水抽出物を酢酸エチ
ルで再抽出したもののクロマトグラム、Bは本発
明菌糸体のクロマトグラムであり、これらは、本
発明のマンネンタケ菌糸体が天然のマンネンタケ
子実体と極めて近似した成分を含有することを示
している。
つぎに実施例を挙げて本発明をさらに詳しく説
明する。
実施例 1〜17
ポテト・デキストロース寒天培地(デイフコ社
製)39gを水1000mlに分散、溶解させ、100mlフ
ラスコに20mlづつ分注し、120℃で30分間オート
クレーブ処理した後、冷却してPDA培地を調製
した。これに、マンネンタケ種菌糸((株)河付式椎
葺研究所より入手)1白金耳接種し、暗所におい
て、25℃で14日間静置培養してマンネンタケ菌糸
体の種培養を得た。
一方、つぎの第1表に示す割合でグルコースお
よび小麦胚芽を滅菌水に分散、溶解し、500ml容
の三角フラスコに150mlづつ分注し、綿栓をし、
アルミホイルで覆つた後、121℃で30分間オート
クレーブ処理し、ついで、室温まで冷却して液体
培地を調製した。
この各液体培地に、無菌条件下、前記の種培養
を3白金耳づつ接種し、25℃の暗所にて、振盪培
養器(220r.p.m.)上で2週間培養した。
培養終了後、培養液を10000r.p.m.で10分間遠
心分離し、上清を除き、沈殿物に適当量のエタノ
ールを加え、激しく振盪した。これをブフナー
斗上で吸引過し、さらに、エタノールで洗浄
し、充分過し、重量を測定して菌糸体の収量と
した。結果を第1表に示す。なお、第1表には、
対照として、液体培地としてポテト・デキストロ
ース・ブロスを用いて同様にマンネンタケ菌糸体
を培養した場合の結果も示す。
TECHNICAL FIELD The present invention relates to a health food made of cultured mycelium of C. chinensis. Stone mushroom is a basidiomycete that belongs to the order Polygonum and the family Sarnocotyaceae.It is also known as Ganoderma, and has been prized as an excellent herbal medicine in China since ancient times. In recent years, much research has been carried out in Japan to scientifically elucidate the active ingredients of Cinnamon mushroom, and its anticancer, antihypertensive,
Its anti-hyperlipidemic effects are gradually becoming clearer, and various attempts have been made to isolate the active ingredient and use it as a medicine, and to use the mushroom itself as a so-called health food. However, Cinnamon mushrooms originally grow very rarely in nature even in China, making them extremely difficult to obtain and very expensive. Recently, in our country, it has become possible to artificially cultivate Cinnamon mushrooms and they are relatively easy to obtain, but they are still expensive and require a long period of 2 to 5 years to grow. In addition, there is a problem in that many of the artificially cultivated stone mushrooms contain different ingredients compared to natural ones. In view of these circumstances, the present inventors conducted extensive research in order to easily and inexpensively obtain a stone mushroom that has the same or similar components as natural ones, and unexpectedly found a specific A liquid medium having the following composition is extremely effective for cultivating the mycelium of C. chinensis, and it is possible to obtain the mycelium of C. chinensis in a short period of time, in good yield, and at low cost. It has been found that it is suitable as As mentioned above, artificial cultivation of Cinnamon lucidum has already been carried out, but this is cultivation of the fruiting body of Cinnamon lucidum, and as in the present invention, the mycelium of Cinnamon lucidum is efficiently cultured in liquid to produce components that resemble natural fruiting bodies. There have been no known examples of mycelia having this. Thus, the present invention provides a novel mycelium culture food containing a mycelium containing components similar to natural fruiting bodies, which is obtained by liquid culture in a liquid medium with a specific composition. According to the present invention, by using 0.2 to 10 w/v% of glucose and 0.2 to 2 w/v% of wheat germ as essential components, it is possible to obtain and culture natural L. chinensis mycelium in a short period of time, at low cost, and in good yield. After completion, the mycelium is separated from the culture and can be used as it is as normal mushrooms or as a health food in a known form according to a conventional method. It can be used in the same way as health foods using That is, in order to obtain the Moscanthus mycelium of the present invention, first, the Moscanthus mycelium is liquid cultured in a liquid medium containing glucose and wheat germ as essential components. The glucose and wheat germ used as the medium components may be any of those commonly available as medium components. Glucose is used in a proportion of 0.2 to 10 w/v%, preferably 1 to 8 w/v%, based on the total amount of the medium. Even if the amount of glucose is lower than 0.2 w/v%, and even if it exceeds 10 w/v%, the yield of mycelium decreases. Wheat germ is based on the total amount of medium.
It is used in a proportion of 0.2 to 2 w/v%, preferably 0.5 to 1.0 w/v%. If the amount of wheat germ is lower than 0.2w/v%, the mycelium yield will decrease;
Exceeding this will be economically disadvantageous. In particular, in the present invention, it is preferable that the weight ratio of wheat germ: glucose in the liquid medium is 1:1 to 8.
This improves the yield of C. chinensis mycelium. Optionally, the liquid medium may contain mineral components such as salts such as phosphorus, manganese, magnesium, calcium, iron, etc., as well as other grain germs, rice bran, etc.
Other nutritional ingredients such as corn staple liquor, vitamins, nucleic acids, amino acids, starch, yeast extract, peptone, etc. may be added as appropriate. The liquid medium can be prepared according to a conventional method, for example, each predetermined component is added to sterilized water and dispersed and dissolved. The resulting medium is typically 120~
After being sterilized at 130°C for 15 to 30 minutes, it is used for culturing the Cinderella mycelium. Cultivation of C. chinensis mycelium is carried out under aerobic conditions by inoculating an appropriate amount of seed mycelia into the liquid medium. The seed hyphae to be used may be any species belonging to the Basidiomycete order, the order Aridaceae, and the hyphae can be obtained from, for example, Kawamura Shiibuki Institute Co., Ltd. (1-1-11 Aoba-cho, Fujieda City, Shizuoka Prefecture). Usually, the amount of seed mycelia inoculated is about 5 to 10 mg/100 ml of medium, and under stirring at 200 to 300 rpm, the temperature
By culturing in the dark for 7 to 21 days at 25 to 30°C and an aeration rate of 0.5 to 3.0 vvm, a high yield of C. monocytogenes mycelium having components similar to those of natural C. monocytogenes fruiting bodies can be obtained ( For example, with this culture, it is possible to achieve a mycelium yield that is 9 to 50 times that of potato dextrose broth (PDB) medium, which is used for conventional seed culture for artificial cultivation of C. After the cultivation is completed, the mycelium is separated from the obtained culture. This separation can be carried out according to conventional methods such as filtration and centrifugation. Note that since useful components are accumulated in the culture solution remaining after the mycelium has been separated, it can also be processed by concentration to dryness and used in the same way as the mycelium. The mycelium thus obtained generally has a diameter of 1 to 5.
It has a spherical shape of mm, has the unique texture and flavor of mushrooms, and has the aromatic flavor of wheat germ.It can be used as a health food as it is, and can be eaten using normal cooking methods. For example, it can be soup, tsukudani, etc. It can also be dried in a conventional manner, crushed if necessary, and combined with a food-acceptable carrier to form powders, tablets, pills, granules, capsules, etc. It can also be used as a nourishing and tonic ingredient. The attached FIGS. 1 and 2 show gas chromatograms and thin-layer chromatograms of extracts obtained by hot water extraction of C. chinensis cultured mycelium obtained in the present invention (Example 2 described below) and further extraction with ethyl acetate. show. The conditions for each chromatography are as follows. Gas chromatography Model used: Shimadzu GC-7A; Column 2%
OV-1, Uniport HP (60-80 mesh), 3
mm x 200cm; Column temperature: Hold at 150℃ for 8 minutes, then increase to 230℃ in 80 minutes; Vaporization chamber temperature: 280
°C; Detector: F1D. In addition, the sample was prepared according to the usual method.
Converted to TMS. Thin layer chromatography plate: Merck silica gel; developing solvent:
Chloroform-methanol (9:1): Color development: I 2
and ultraviolet rays (in Figure 2, the spots indicated by dotted lines develop color with I2 , and the spots indicated with solid lines develop color under an ultraviolet lamp and are strongly colored with I2 ). In FIGS. 1 and 2, chromatogram A is a chromatogram of a hot water extract of a natural rock fruiting body re-extracted with ethyl acetate, and B is a chromatogram of the mycelium of the present invention. This shows that the C. latinum mycelium of the invention contains components that are extremely similar to those of the natural C. latinum fruiting body. Next, the present invention will be explained in more detail with reference to Examples. Examples 1 to 17 39 g of potato dextrose agar medium (manufactured by Difco) was dispersed and dissolved in 1000 ml of water, dispensed into 100 ml flasks in 20 ml portions, autoclaved at 120°C for 30 minutes, and then cooled to form a PDA medium. Prepared. This was inoculated with one platinum loop of C. chinensis seed mycelia (obtained from Kawatsuki Shiibuki Research Institute, Inc.), and cultured stationary in the dark at 25° C. for 14 days to obtain a seed culture of C. chinensis mycelium. On the other hand, dissolve and dissolve glucose and wheat germ in sterilized water in the proportions shown in Table 1 below, dispense 150 ml each into 500 ml Erlenmeyer flasks, and cap with cotton plugs.
After covering with aluminum foil, it was autoclaved at 121°C for 30 minutes, and then cooled to room temperature to prepare a liquid medium. Three platinum loops of the above seed culture were inoculated into each liquid medium under aseptic conditions, and cultured for 2 weeks in a shaking incubator (220 rpm) in the dark at 25°C. After the culture was completed, the culture solution was centrifuged at 10,000 rpm for 10 minutes, the supernatant was removed, and an appropriate amount of ethanol was added to the precipitate, followed by vigorous shaking. This was suctioned and filtered on a Buchner funnel, washed with ethanol, thoroughly filtered, and weighed to determine the mycelium yield. The results are shown in Table 1. Furthermore, in Table 1,
As a control, the results are also shown when the same method was used to culture C. chinensis mycelium using potato dextrose broth as a liquid medium.
【表】
この結果から明らかなごとく、本発明の液体培
地を用いると、非常に高い菌糸体収量が得られ、
ことに、小麦胚芽:グルコースの比を1:1〜8
にすると収量が高くなる。
得られた菌糸体は、いずれも1〜5mmの径の球
状をなし、これを25℃で12〜24時間風乾して本発
明の健康食品を得た。
実施例 18
ジヤーフアーメンターを用いてマンネンタケ菌
糸体の培養をつぎのとおり行なつた。
ジヤーフアーメンター(10容)のジヤー中で
グルコース100gおよび小麦胚芽25gを、沸騰冷
却した水道水5と混合し、ついで、ジヤーを密
栓して121℃で30分間オートクレーブ処理して液
体培地を調製した。ジヤーをジヤーフアーメンタ
ーに取り付け、同じ培地で25℃、14日間振盪培養
した種菌糸培養物150mlを無菌条件下に接種した。
300r.p.m.の撹拌下、3.0/分の流速で空気を通
気しながら、28℃にて14日間培養した。得られた
培養物をガーゼで過して菌糸体0.84Kg(湿潤重
量)および培養液3.5を得た。
得られた菌糸体を25℃で12〜24時間風乾して本
発明の健康食品を得た。[Table] As is clear from the results, when the liquid medium of the present invention is used, a very high mycelium yield can be obtained.
In particular, the wheat germ:glucose ratio is 1:1 to 8.
The yield will be higher. The obtained mycelium had a spherical shape with a diameter of 1 to 5 mm, and was air-dried at 25° C. for 12 to 24 hours to obtain the health food of the present invention. Example 18 Using a jar fermentor, the mycelium of C. chinensis was cultured as follows. A liquid medium was prepared by mixing 100 g of glucose and 25 g of wheat germ with boiled and cooled tap water in a jar of a jar fermenter (10 volumes), then sealing the jar and autoclaving at 121°C for 30 minutes. did. The jar was attached to a jar fermentor, and 150 ml of a seed mycelial culture, which had been cultured with the same medium at 25° C. for 14 days with shaking, was inoculated under aseptic conditions.
The cells were cultured at 28° C. for 14 days while stirring at 300 rpm and aerating air at a flow rate of 3.0/min. The resulting culture was passed through gauze to obtain 0.84 Kg (wet weight) of mycelium and 3.5 kg of culture solution. The obtained mycelium was air-dried at 25°C for 12 to 24 hours to obtain the health food of the present invention.
第1図および第2図は、各々、本発明の菌糸体
と天然のマンネンタケ子実体の成分を比較するガ
スクロマトグラムおよび薄層クロマトグラムであ
る。
FIGS. 1 and 2 are gas chromatograms and thin layer chromatograms, respectively, comparing the components of the mycelium of the present invention and natural L. lucidum fruiting bodies.
Claims (1)
0.2〜2w/v%を必須成分とする液体培地中で培
養して得られるマンネンタケ菌糸体からなること
を特徴とする健康食品。 2 該培地中の小麦胚芽:グルコースの重量比が
1:1〜8である前記第1項の健康食品。[Claims] 1. Glucose 0.2-10w/v% and wheat germ
1. A health food characterized by comprising a mycelium of C. chinensis obtained by culturing it in a liquid medium containing 0.2 to 2 w/v% as an essential component. 2. The health food according to item 1 above, wherein the weight ratio of wheat germ to glucose in the medium is 1:1 to 8.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58151848A JPS6043357A (en) | 1983-08-19 | 1983-08-19 | Health food containing cultured mycelia of forms japonicus |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58151848A JPS6043357A (en) | 1983-08-19 | 1983-08-19 | Health food containing cultured mycelia of forms japonicus |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6043357A JPS6043357A (en) | 1985-03-07 |
JPS633577B2 true JPS633577B2 (en) | 1988-01-25 |
Family
ID=15527589
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58151848A Granted JPS6043357A (en) | 1983-08-19 | 1983-08-19 | Health food containing cultured mycelia of forms japonicus |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6043357A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0855B2 (en) * | 1987-10-20 | 1996-01-10 | 呉羽化学工業株式会社 | Foods containing granular bacterial strains of Suehirotake |
JP2814209B2 (en) * | 1995-03-29 | 1998-10-22 | パワフル健康食品株式会社 | Anti-mutagenic food |
JP5243490B2 (en) | 2010-06-14 | 2013-07-24 | 株式会社遠藤製作所 | Hollow club head for golf club |
JP6357574B1 (en) * | 2017-09-13 | 2018-07-11 | 有限会社プレステックス | Ganoderma mycelium culture method in soybean medium and Ganoderma mycelium health food containing soybean |
-
1983
- 1983-08-19 JP JP58151848A patent/JPS6043357A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6043357A (en) | 1985-03-07 |
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