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JPS62186784A - Water-based solid medium - Google Patents

Water-based solid medium

Info

Publication number
JPS62186784A
JPS62186784A JP61026540A JP2654086A JPS62186784A JP S62186784 A JPS62186784 A JP S62186784A JP 61026540 A JP61026540 A JP 61026540A JP 2654086 A JP2654086 A JP 2654086A JP S62186784 A JPS62186784 A JP S62186784A
Authority
JP
Japan
Prior art keywords
medium
gum
solid medium
water
locust bean
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.)
Pending
Application number
JP61026540A
Other languages
Japanese (ja)
Inventor
Takatoshi Koda
隆俊 香田
Iwao Asai
以和夫 浅井
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.)
San Ei Kagaku Co Ltd
Sanei Kagaku Kogyo KK
Original Assignee
San Ei Kagaku Co Ltd
Sanei Kagaku Kogyo 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 San Ei Kagaku Co Ltd, Sanei Kagaku Kogyo KK filed Critical San Ei Kagaku Co Ltd
Priority to JP61026540A priority Critical patent/JPS62186784A/en
Publication of JPS62186784A publication Critical patent/JPS62186784A/en
Pending legal-status Critical Current

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  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

PURPOSE:To obtain the titled medium for the proliferation of living vegetable or animal cell or microorganism, by using xanthan gum in combination with locust bean gum as a colloid. CONSTITUTION:The objective medium contains xanthan gum and locust bean gum as a colloid. The weight ratio of the gum components id preferably 1:1. EFFECT:Since the medium is transparent, the behavior of the cell, etc., in the medium can be easily observed. The proliferation and growth of cultured cell, tissue, etc., are rapid in the medium.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発明は、動物、植物の生活活性細胞組織あるいは、
微生物例えば、酵母、細菌等を人工的に増殖させるため
の培地に係るものでるる。
[Detailed Description of the Invention] [Industrial Application Field] This invention relates to the use of living active cell tissues of animals and plants;
This applies to media for artificially growing microorganisms such as yeast and bacteria.

〔従来の技術〕[Conventional technology]

生活活性を有する植物、動物の細胞組織、微生物等を培
養する固体培地の材料膠質としては、通常寒天が使用さ
れ1いて、その他の脚質はほとんど便用されていηい。
Agar is usually used as the material for solid media for culturing living active plants, animal cell tissues, microorganisms, etc., and other leg substances are rarely used.

ここに、固体培地とは流体帛地(ルを質を原則として含
寸〃い)にたいする呼称であって、培地の国有取分の1
つとして噌質を使用しゲル化させた水性系をいう。
Here, the solid medium is a name for a fluid fabric (including dimensions based on quality as a general rule), and is one of the nationally owned shares of the medium.
It refers to an aqueous system that uses soybean paste to form a gel.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

寒天を使用した固体培地は、常に白濁し、その内部を外
部から肉眼、あるいは顕微鏡をもって検査ないし観察を
することが困難である。
A solid medium using agar is always cloudy, making it difficult to inspect or observe its interior from the outside with the naked eye or a microscope.

つれて、これに例えば生活活性植物細胞を植付けてカル
スを得、あるいは植物成体を得ようとするとき、そのカ
ルスの増殖過程や発根状態その他の細胞塊ないし成体の
挙動を観察することは、極めて困難である。
When attempting to obtain a callus or an adult plant by, for example, planting living active plant cells, observing the growth process of the callus, the state of rooting, and other behaviors of the cell mass or the adult plant is It is extremely difficult.

〔発明の課題〕[Problem of invention]

そこで、透明なかつ工業的期待に添いうる固体培地の創
出が当菓者の課題である。
Therefore, our challenge is to create a solid medium that is transparent and meets industrial expectations.

この発明は、この課題に対する1つの解答であり、この
課題を工業的に有利に解決したものである。
This invention is one solution to this problem, and is an industrially advantageous solution to this problem.

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

この発明を以下に詳しく説明する。 This invention will be explained in detail below.

従来の寒天に替へて、この発明が採用する膠質は、公知
のもののうち、キサンタンカムとローカストビ−ンガム
である。キサンタンカムもローカストビーンガムも何れ
も単独ではゲル化しないが、両者を併用すればゲル化し
て澄明な固体になるという性質を示す。即ち、両者を併
合して膠質となる。
In place of the conventional agar, the colloids employed in this invention are xanthancum and locust bean gum, among the known ones. Neither xanthancum nor locust bean gum will gel when used alone, but when used together, they will gel and become a clear solid. In other words, the two are combined to form a colloid.

この発明の培地は、ゲル化させるためには両材料の混合
割合は、任意でりるが、培地の最適固状を得るだめVζ
は両者をほぼ等重量にするのがよい。
In the medium of this invention, the mixing ratio of both materials can be determined arbitrarily in order to form a gel, but in order to obtain the optimum solidity of the medium, Vζ
It is best to make both of them approximately equal in weight.

キサンタンガムとローカストビーンガムの混合物を水性
系とする。その際両者の合計直裁が水にたいし、約0.
5〜1.0%(重量、以下同じ)になるように配合し、
均質にする。この糸を加熱してゾル化させ、これを冷却
してゲル化させ、室温にし固化させる。
A mixture of xanthan gum and locust bean gum is used as an aqueous system. At that time, the total direct judgment of both is about 0.
Blend so that it is 5 to 1.0% (weight, same below),
Make it homogeneous. The thread is heated to form a sol, then cooled to form a gel, and allowed to cool to room temperature and solidify.

この際、この培地に、予めチン素、リン酸、カリ系各物
質、公知の細胞増殖ホルモン、例えばオーキシン、サイ
トカイニン、など及び、微量成分を添加してよいことは
明らかである。
At this time, it is clear that tin, phosphoric acid, potassium-based substances, known cell growth hormones such as auxin and cytokinin, and trace components may be added to the medium in advance.

この上うKして得だものがこの発明の目的物である澄明
な水性固体培地である。
An additional benefit is the clear aqueous solid medium that is the object of this invention.

ここに、この発明はその目的を達しおえる。Here, this invention achieves its purpose.

〔)ε明の作用及び効果〕[) Effects and effects of εming]

このものは、次の特徴を有している。 This product has the following characteristics.

■澄明でりるから外部から培地内部の拙@等の挙動状1
照を容易に鶴察することができる。
■Since it is clear, the behavior of me @ etc. from the outside to the inside of the medium 1
The crane can easily see the light.

■培養細胞、組織等の増殖、生長が寒天培地に比べて早
い。その理由は、今のところ明らかではない。
■Proliferation and growth of cultured cells and tissues is faster than on agar media. The reason for this is not clear at this time.

以下に、実験例を記して上記判断の正しいことを説明す
る。
Below, the correctness of the above judgment will be explained by describing an experimental example.

説  明 ■培地組成 ア、キュウリ種子、ハツカダイコン種子・・・・・・水
のみイ、ヨウシュヤマゴボウ及びタバコのカルス・旧・
・以下に記す 同一培地を使用した。
Explanation ■Medium composition A, cucumber seeds, radish seeds... water only, mountain burdock, and tobacco callus/old...
- The same medium described below was used.

硝酸アンモニウム           1650My
硝酸カリウム              1900〃
リン酸第1カリウム           l ’7Q
//塩化カルシウム・ 2H20440η 硫酸マグネシウム・7H20370を 硫酸マンガン−4FI20          22.
31/硼  酸                  
   6.27硫酸亜鉛・4H208,6□ 沃化カリウム              0.88N
モリブデン酸ナトリウム・2H200,25〃硫酸第1
銅−5H200,025// 塩化コバルト・6H200,025〃 EDTAナトリウム               3
7.3 〃硫酸第1鉄・7Hz0          
 27.8Ilミオイノシトール          
        1OOqチアミン塩酸塩      
       0.4〃2.4−ジクロロフェノキシ酢
酸o、22qショ糖                
3(1以上の成分に上記表中の夫々の膠質を加えて、水
にて1gとし、I)Hを5.7に調整した均質固形培地
を三角フラスコに入れアルシミ洒(通気可能、水の蒸発
は困難)で栓をしたのち、殺菌(120°C・15分間
)したものを室温に下げ供試。
Ammonium nitrate 1650My
Potassium nitrate 1900〃
Potassium phosphate l '7Q
//Calcium chloride・2H20440η Magnesium sulfate・7H20370 with manganese sulfate-4FI20 22.
31/boric acid
6.27 Zinc sulfate/4H208,6□ Potassium iodide 0.88N
Sodium molybdate 2H200,25 sulfuric acid 1st
Copper-5H200,025// Cobalt chloride/6H200,025 Sodium EDTA 3
7.3 Ferrous sulfate, 7Hz0
27.8Il myo-inositol
1OOq thiamine hydrochloride
0.4 2.4-dichlorophenoxyacetic acid o, 22q sucrose
3 (Add each colloid in the table above to one or more ingredients, make 1 g with water, and adjust the I)H to 5.7. Place the homogeneous solid medium in an Erlenmeyer flask and add it to the aluminum bottle (aerated, water-filled). (difficult to evaporate), then sterilized (120°C for 15 minutes), cooled to room temperature, and tested.

■培養条件 温度 25°C 照明  3. OOO/L/クス 培養  ギュウリ及びハツカダイコンの種子   7日
間ヨウシュヤマゴボウ及びタバコのカルス35〃■ヨウ
シユヤマゴボウ及びタバコの新鮮カルスの植付i0.3
r■生長度 ア、キュウリ及びハツカダイコンの種子発芽では、茎長
及び根長(醍)で示す。) イ、ヨウシュヤマゴボウ及びタバコのカルスでは、収得
カルヌの新鮮重量(2)で示す。
■Culture conditions Temperature 25°C Lighting 3. OOO/L/Cultivation Cucumber and radish seeds 7 days Pokeweed and tobacco callus 35〃■ Planting of fresh Pokeweed and tobacco callus i0.3
r■Growth degree A: Seed germination of cucumbers and radish is indicated by stem length and root length (double). ) For callus of pokeweed and tobacco, it is expressed as the fresh weight of the harvested callus (2).

Claims (1)

【特許請求の範囲】[Claims] 膠質としてキサンタンガムとローカストビーンガムとを
併用してなることを特徴とする植物、動物の生活活性細
胞、あるいは微生物を増殖させるための水性固体培地。
An aqueous solid medium for growing active cells of plants and animals, or microorganisms, characterized by using xanthan gum and locust bean gum as colloids in combination.
JP61026540A 1986-02-07 1986-02-07 Water-based solid medium Pending JPS62186784A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61026540A JPS62186784A (en) 1986-02-07 1986-02-07 Water-based solid medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61026540A JPS62186784A (en) 1986-02-07 1986-02-07 Water-based solid medium

Publications (1)

Publication Number Publication Date
JPS62186784A true JPS62186784A (en) 1987-08-15

Family

ID=12196329

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61026540A Pending JPS62186784A (en) 1986-02-07 1986-02-07 Water-based solid medium

Country Status (1)

Country Link
JP (1) JPS62186784A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2500721A (en) * 2012-03-30 2013-10-02 Provost Fellows & Scholars College Of The Holy Undivided Trinity Of Queen Elizabeth Near Dublin Cell culture medium additive comprising a xanthan polysaccharide and a mannan polysaccharide

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2500721A (en) * 2012-03-30 2013-10-02 Provost Fellows & Scholars College Of The Holy Undivided Trinity Of Queen Elizabeth Near Dublin Cell culture medium additive comprising a xanthan polysaccharide and a mannan polysaccharide

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