JPH09100202A - Anti-organism agent - Google Patents
Anti-organism agentInfo
- Publication number
- JPH09100202A JPH09100202A JP27822095A JP27822095A JPH09100202A JP H09100202 A JPH09100202 A JP H09100202A JP 27822095 A JP27822095 A JP 27822095A JP 27822095 A JP27822095 A JP 27822095A JP H09100202 A JPH09100202 A JP H09100202A
- Authority
- JP
- Japan
- Prior art keywords
- capsaicin
- agent
- organism
- organism agent
- algae
- 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
Links
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、藻類等の各種生物に対
する増殖抑制剤に関する。TECHNICAL FIELD The present invention relates to a growth inhibitor for various organisms such as algae.
【0002】[0002]
【従来の技術】藻類(アオコ)の増殖は水田・湖沼・芝
生等様々な場面で問題となっている。水田では水面に増
殖した藻類により太陽光線が遮られ、水温が上がらなく
なったり、土の表層剥離の原因となる。夏場の湖沼では
アオコの大量発生により水道水の悪臭などの問題が発生
する。芝生では藻類の増殖により美観が著しく損なわれ
るなどの問題が発生している。噴水などでも藻類の増殖
により美観が損なわれ、その清掃作業に少なからぬ人手
と費用が費やされている。さらに、海洋性の藻類(植物
プランクトン)の増殖、すなわち赤潮は沿岸漁業に毎年
莫大な損害を与えている。2. Description of the Related Art Propagation of algae has become a problem in various fields such as paddy fields, lakes, and lawns. In the paddy field, the algae that grow on the surface of the water block the sun's rays, which prevents the water temperature from rising and causes the surface layer of the soil to peel off. In lakes in summer, problems such as bad smell of tap water occur due to the large amount of blue-green algae. On the lawn, there are problems such as aesthetic deterioration due to the growth of algae. Even in fountains, the growth of algae impairs the aesthetics, and a considerable amount of manpower and money are spent on the cleaning work. Moreover, the growth of marine algae (phytoplankton), or red tide, causes immense damage to coastal fisheries every year.
【0003】しかしながら、藻類の増殖を抑制し、かつ
環境に対する負荷が少ない薬剤は未だ見いだされていな
い。農薬でACN(2−アミノ−3−クロル−1,4−ナ
フトキノン)等が抗藻類剤として実用化されているが、
魚毒性が強く、使用範囲はごく狭いものとなっている。However, a drug that suppresses the growth of algae and has a low environmental load has not yet been found. ACN (2-amino-3-chloro-1,4-naphthoquinone), etc. has been put to practical use as an anti-algal agent as a pesticide.
It is highly toxic to fish and its use range is extremely narrow.
【0004】[0004]
【発明が解決しようとする課題】本発明は環境に対し負
荷が小さく、また人体に対する毒性の少ない抗生物剤を
提供することを目的とする。SUMMARY OF THE INVENTION It is an object of the present invention to provide an antibiotic agent which has a low load on the environment and is less toxic to the human body.
【0005】[0005]
【課題を解決するための手段】本発明者らは、上記課題
を解決するために鋭意努力した結果、カプサイシン類が
藻類等の生物の増殖抑制に極めて有効であることを見出
し本発明を解決した。特許請求の範囲に記載の各請求項
の発明により、本課題を解決することができた。即ち、
本発明は、カプサイシン類を有効成分とする抗生物剤で
ある。Means for Solving the Problems As a result of diligent efforts to solve the above problems, the present inventors have found that capsaicins are extremely effective in suppressing the growth of organisms such as algae, and solved the present invention. . The present invention can be solved by the inventions of the claims described in the claims. That is,
The present invention is an antibiotic agent containing capsaicins as an active ingredient.
【0006】本発明に用いるカプサイシン類の構造式は
下記の式1に示すものである。The structural formula of the capsaicins used in the present invention is shown in the following formula 1.
【0007】[0007]
【式1】 (Equation 1)
【0008】例示すれば、カプサイシン[Rが(CH2)4CH=
CHCH(CH3)2]、ジヒドロカプサイシン[Rが(CH2)6CH(CH
3)2]、ノルカプサイシン[Rが(CH2)3CH=CHCH(C
H3)2]、ホモカプサイシン[Rが(CH2)5CH=CHCH(C
H3)2]、オクタン酸バニリルアミド[Rが(CH2)6CH3]、
ノナン酸バニリルアミド[Rが(CH2)7CH3]などが挙げら
れるが、これらに限定されるものではない。For example, capsaicin [R is (CH 2 ) 4 CH =
CHCH (CH 3 ) 2 ], dihydrocapsaicin [R is (CH 2 ) 6 CH (CH
3 ) 2 ], norcapsaicin [R is (CH 2 ) 3 CH = CHCH (C
H 3 ) 2 ], homocapsaicin [R is (CH 2 ) 5 CH = CHCH (C
H 3 ) 2 ], vanillyl octanoate [R is (CH 2 ) 6 CH 3 ],
Nonanoic acid vanillyl amide [R is (CH 2 ) 7 CH 3 ] and the like can be mentioned, but the invention is not limited thereto.
【0009】カプサイシン類は純品を使用しても良い
が、より安価な食品用のトウガラシエキスを使用しても
良い。Capsaicins may be pure products, but cheaper capsicum extract for food may be used.
【0010】抗生物剤は乳化剤を添加して乳剤とした
り、固体担体にカプサイシンを付着させ粉剤とするな
ど、いかなる形態をとっても良い。乳化剤としては、各
種脂肪酸エステル、例えばグリセリン脂肪酸エステル、
ショ糖脂肪酸エステル、ソルビタン脂肪エステル、プロ
ピレングリコール脂肪酸エステルが、担体としては例え
ば、ハイドロキシアパタイト、シリカゲル、ゼオライ
ト、炭酸カルシウム、コルク粉末、ベントナイト等が本
発明に使用されるが、その他薬剤学的に許容できる乳化
剤、担体等も本発明に包含する。また、表2及び表3に
示すように、カプサイシン類を担体や乳化剤に保持させ
ると、藻類の増殖抑制効果が高められる。The antibiotic agent may be in any form such as adding an emulsifier to form an emulsion, or capsaicin to a solid carrier to form a powder. As the emulsifier, various fatty acid esters, for example, glycerin fatty acid ester,
Sucrose fatty acid ester, sorbitan fatty acid ester, propylene glycol fatty acid ester are used as the carrier in the present invention, for example, hydroxyapatite, silica gel, zeolite, calcium carbonate, cork powder, bentonite, etc. Possible emulsifiers, carriers and the like are also included in the present invention. Further, as shown in Tables 2 and 3, when capsaicins are held in a carrier or an emulsifier, the effect of suppressing the growth of algae is enhanced.
【0011】[0011]
【実施例】実施例により本発明を具体的に説明するが、
本発明は、これらの実施例に限定されない。EXAMPLES The present invention will be specifically described with reference to examples.
The invention is not limited to these examples.
【0012】実施例1 藻類(Oocystis sp.)の増殖抑
制 被験藻類のOocystis sp.は家庭用水槽から分離し、同定
したものを用いた。カプサイシン(Sigma社)、ジヒド
ロカプサイシン(Sigma社)をそれぞれエタノールにて
溶解し、1%(10mg/ml)の溶液を調製した。本溶液10μl
を細胞培養用6穴プラスティックプレート(Costar 359
6)の底面に滴下し、風乾した。各ウェルに、C培地
(「藻類研究法」共立出版参照)に3,500 cells/mlの細
胞濃度に調製したOocystis sp.細胞懸濁液10mlを分注し
た(薬剤の終濃度は10μg/ml)。対照として薬剤無添加
の系を置いた。照度5,000 lx、温度25℃の条件で7日間
インキュベート後、Oocystis sp.の増殖量を濁度(A680
nm)で測定した。結果を表1に示す。Example 1 Inhibition of Algae ( Oocystis sp.) Growth Oacystis sp. Of the test algae was isolated from a domestic aquarium and identified. Capsaicin (Sigma) and dihydrocapsaicin (Sigma) were each dissolved in ethanol to prepare a 1% (10 mg / ml) solution. 10 μl of this solution
6-well plastic plate for cell culture (Costar 359
It was dripped on the bottom of 6) and air dried. To each well, 10 ml of Oocystis sp. Cell suspension prepared at a cell concentration of 3,500 cells / ml in C medium (see “Algae Research Method” Kyoritsu Shuppan) was dispensed (final concentration of drug was 10 μg / ml). As a control, a drug-free system was set up. After incubating for 7 days under the conditions of illuminance of 5,000 lx and temperature of 25 ° C, the growth amount of Oocystis sp.
nm). Table 1 shows the results.
【0013】[0013]
【表1】 [Table 1]
【0014】実施例2 各種固体担体に吸着させたカプ
サイシンの抗藻類活性 カプサイシン(Sigma社)をエタノールにて溶解し、シ
リカゲル(和光純薬)、ヒドロキシアパタイト(和光純
薬)、ゼオライト(和光純薬)、炭酸カルシウム(和光
純薬)、コルク粉末(φ1mm)の各種固体担体に1%(w/w)
の重量比で吸着させた。展着剤として食品添加物のグリ
セリン脂肪酸エステル(理研ビタミン)を5%(w/w)用い
た。これらの薬剤を細胞培養用のプラスティック200ml
ボトル(Falcon 3110)に100mg投入した。ボトルに実施
例1と同様に調製したOocystis sp.細胞懸濁液50mlを分
注し、実施例1の培養条件で光照射下にて振盪培養した
(カプサイシン終濃度20μg/ml)。対照としてエタノー
ルに溶解したカプサイシンを20μg/mlの終濃度になるよ
うにボトルの底面に展着した系を置いた。増殖量は藻類
細胞を遠心して集め、クロロフィルをアセトン抽出し、
分光光度計にて定量して測定した。結果を表2に示す。Example 2 Anti-algal activity of capsaicin adsorbed on various solid supports Capsaicin (Sigma) was dissolved in ethanol, and silica gel (Wako Pure Chemical), hydroxyapatite (Wako Pure Chemical), zeolite (Wako Pure Chemical) ), Calcium carbonate (Wako Pure Chemical Industries, Ltd.), 1% (w / w) on various solid carriers such as cork powder (φ1mm)
Was adsorbed at a weight ratio of. As a spreading agent, 5% (w / w) of glycerin fatty acid ester (RIKEN vitamin) as a food additive was used. 200 ml of plastic for cell culture
100 mg was added to a bottle (Falcon 3110). 50 ml of the Oocystis sp. Cell suspension prepared in the same manner as in Example 1 was dispensed into a bottle and shake-cultured under light irradiation under the culture conditions of Example 1 (capsaicin final concentration 20 μg / ml). As a control, a system in which capsaicin dissolved in ethanol was spread on the bottom surface of the bottle to a final concentration of 20 μg / ml was placed. The amount of growth was collected by centrifuging algal cells, extracting chlorophyll with acetone,
It measured quantitatively with the spectrophotometer. Table 2 shows the results.
【0015】[0015]
【表2】 [Table 2]
【0016】実施例3 カプサイシン乳化剤の抗藻類活
性 カプサイシン(Sigma社)を食品添加物のグリセリン脂
肪酸エステル(理研ビタミン)を用いて乳化させ、カプ
サイシン乳剤を得た。乳剤中のカプサイシン濃度は2%(w
/w)、脂肪酸エステルは5%(w/w)とした。これらの薬剤を
細胞培養用のプラスティック200mlボトル(Falcon 311
0)に25、50、100μl投入し、実施例2と同条件でOocys
tis sp.を培養した(カプサイシン終濃度20μg/ml)。
対照としてエタノールに溶解したカプサイシンを20μg/
mlの終濃度になるようにボトルの底面に展着した系を置
いた。増殖量は実施例2と同様に測定した。結果を表3
に示す。Example 3 Anti-algal activity of capsaicin emulsifier Capsaicin (Sigma) was emulsified with glycerin fatty acid ester (RIKEN vitamin) as a food additive to obtain a capsaicin emulsion. The concentration of capsaicin in the emulsion is 2% (w
/ w) and the fatty acid ester was 5% (w / w). These drugs were added to plastic 200 ml bottles for cell culture (Falcon 311
0, 25, 50 and 100 μl were added to Oocys under the same conditions as in Example 2.
The tis sp. was cultured (capsaicin final concentration 20 μg / ml).
20 μg of capsaicin dissolved in ethanol as a control
The spread system was placed on the bottom of the bottle to a final concentration of ml. The amount of proliferation was measured as in Example 2. Table 3 shows the results
Shown in
【0017】[0017]
【表3】 [Table 3]
【0018】[0018]
【発明の効果】本発明により、人体に対して安全であ
り、かつ環境に対する負荷が少ないカプサイシン類を有
効成分とする抗生物剤を市場に供給することが可能とな
る。INDUSTRIAL APPLICABILITY According to the present invention, it is possible to supply to the market an antibiotic agent containing capsaicins as an active ingredient, which is safe for the human body and has a low environmental load.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 佐久間 貞俊 神奈川県小田原市成田540番地 明治乳業 株式会社細胞工学センター内 ─────────────────────────────────────────────────── ─── Continuation of front page (72) Inventor Sadatoshi Sakuma 540 Narita, Odawara-shi, Kanagawa Meiji Dairy Co., Ltd. Cell Engineering Center
Claims (3)
剤。1. An antibiotic agent containing capsaicin as an active ingredient.
む請求項1に記載の抗生物剤。2. The antibiotic agent according to claim 1, which comprises a pharmaceutically acceptable carrier or emulsifier.
抗生物剤。3. The antibiotic agent according to claim 1, which is an anti-algal agent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27822095A JPH09100202A (en) | 1995-10-03 | 1995-10-03 | Anti-organism agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27822095A JPH09100202A (en) | 1995-10-03 | 1995-10-03 | Anti-organism agent |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH09100202A true JPH09100202A (en) | 1997-04-15 |
Family
ID=17594291
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27822095A Pending JPH09100202A (en) | 1995-10-03 | 1995-10-03 | Anti-organism agent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH09100202A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005025314A1 (en) * | 2003-09-12 | 2005-03-24 | Aximed As | Capsaicin derivates and the production and use thereof |
-
1995
- 1995-10-03 JP JP27822095A patent/JPH09100202A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005025314A1 (en) * | 2003-09-12 | 2005-03-24 | Aximed As | Capsaicin derivates and the production and use thereof |
JP2007505104A (en) * | 2003-09-12 | 2007-03-08 | アクシメド エーエス | Capsaicin derivatives and their production and use |
US7446226B2 (en) | 2003-09-12 | 2008-11-04 | Aximed As | Capsaicin derivates and the production and use thereof |
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