JPH0213367A - Novel pathogenic microorganisms, herbicides containing the microorganisms, and weed control methods using them - Google Patents

Novel pathogenic microorganisms, herbicides containing the microorganisms, and weed control methods using them

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Publication number
JPH0213367A
JPH0213367A JP63162592A JP16259288A JPH0213367A JP H0213367 A JPH0213367 A JP H0213367A JP 63162592 A JP63162592 A JP 63162592A JP 16259288 A JP16259288 A JP 16259288A JP H0213367 A JPH0213367 A JP H0213367A
Authority
JP
Japan
Prior art keywords
microorganisms
barnyard grass
pathogenic
present
pathogenic microorganism
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
JP63162592A
Other languages
Japanese (ja)
Inventor
Masanobu Arita
有田 政信
Kenichi Yamaguchi
健一 山口
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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
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Application filed by Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP63162592A priority Critical patent/JPH0213367A/en
Publication of JPH0213367A publication Critical patent/JPH0213367A/en
Pending legal-status Critical Current

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  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

NEW MATERIAL:Fusarium oxysporum MH-0008 (FERM 10056). USE:A herbicide selectively killing barnyard millet which is harmful weed in rice field. PREPARATION:Barnyard millet exhibiting disease symptom is collected, sterilized at the surface, placed on an agar medium and cultured at 25 deg.C for 48-72hr to obtain the objective microorganism.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は雑草、特にイネ科重要作物であるイネ、コムギ
等の栽培において有害雑草であるヒエの防除に有効な病
原微生物、該微生物を含有する除草剤およびそれらによ
る雑草防除方法に関するものである。
[Detailed Description of the Invention] [Industrial Application Field] The present invention is a pathogenic microorganism that is effective for controlling weeds, particularly barnyard grass, which is a harmful weed in the cultivation of important crops of the Poaceae family, such as rice and wheat, and a method containing the microorganism. This invention relates to herbicides and methods for controlling weeds using them.

〔従来技術〕[Prior art]

雑草の発生は農家にとって、作物に対する損害と雑草防
除の経費とで、多額の費用を要する。この様な作物に対
して有害な雑草のもたらす損害は、収穫量の減少、作物
の品質低下や雑草中に住む虫や病気等による作物の被害
によるものが主たるものと考えられる。現在では、これ
らの雑草に対する被害を減少させるために主゛として化
学除草剤が使用されている。しかし、最近人間は自分が
食べる食品や住んでいる土地、使用している地下水に対
して化学除草剤の影響を懸念するようになってきた。こ
の主たる対策として現在無農薬栽培作物が多く出てくる
ような風潮となっている。しかしながら、この人力によ
る方法は、労働時間の増加や作業性に問題点が生じてく
る。一方、化学除草剤で除草することが常に困難な難防
除雑草が存在していることも認められている。これらの
化学除草剤の欠点を改善した除草剤として最近微生物除
車側が注目を集めているる、この手法は、天然に存在し
ている微生物(雑草に対する病原菌)を利用したもので
、公害や作物を通しての人体に対する影響が化学除草剤
に比して非常に少ないと考えられ、化学除草剤に変わる
ものとしてますます重要な位置を示しつつある。この重
要性を考えて現在、多くの研究室で研究が行われている
が、特にアメリカでは研究および実用化試験がここ数年
精力的に行われている。これらの例をアメリカ合衆国特
許に見ると、合衆国特許第3.849,104号〔コレ
トトリカム グロエオスボリオイデス ペンズアエスキ
ノメネ(Colletotrichum gloeos
porioi−des Peoz、 aes−chyn
oa+ene)によるノーザンジツイントベッチの防除
〕 ;第3,999.973号(コレトトリカム マル
バラム(Colletotrichum walva−
rum )によるブリツクリーシダその他の雑草の防除
〕 ;第4,263.036号〔フザリウム ロゼウム
カルモラム(Fusarfum roseum Cu1
morus+)によるハイドリラ パーティシラータの
防除〕 ;第4、390.360号(アルタナリアカシ
ェ(Alternariacasiea)によるシック
ルボッドその他の雑草の防除等〕が挙げられる。これら
の中に、アメリカで現在上布されている微生物除草剤と
してデバイン(DsVine、アボット社商品名)及び
コレゴ(Collego。
Weed outbreaks cost farmers a large amount of money due to damage to crops and the cost of weed control. The damage caused by harmful weeds to such crops is thought to be mainly due to reduced yields, deterioration in crop quality, and damage to crops caused by insects and diseases living in weeds. Currently, chemical herbicides are mainly used to reduce the damage caused by these weeds. However, recently humans have become concerned about the effects of chemical herbicides on the food they eat, the land they live on, and the groundwater they use. As a major countermeasure to this problem, there is currently a trend toward many crops being grown without pesticides. However, this manual method causes problems such as an increase in working hours and workability. On the other hand, it is also recognized that there are difficult-to-control weeds that are always difficult to eliminate with chemical herbicides. Recently, microbial herbicides have been attracting attention as a herbicide that improves the shortcomings of these chemical herbicides.This method uses naturally occurring microorganisms (pathogens for weeds) and is effective against pollution and crops. It is thought that the effect on the human body through the chemical herbicides is much lower than that of chemical herbicides, and it is becoming increasingly important as an alternative to chemical herbicides. Considering the importance of this, research is currently being conducted in many laboratories, and research and practical trials have been particularly active in the United States over the past few years. Examples of these can be found in U.S. Patent No. 3,849,104 [Colletotrichum gloeos volioides penzuaescynomene].
porioi-des Peoz, aes-chyn
No. 3,999.973 (Colletotrichum walva-
rum); No. 4,263.036 [Fusarfum roseum Cu1
4, No. 390.360 (Control of Sicklebod and other Weeds by Alternaria casiea)]. The microbial herbicides used are DsVine (trade name of Abbott) and Collego.

アップジテン社商品名)があり、各々特異的強害雑草に
対して除草効果を示している。しかし、イネ科重要作物
であるイネ、コムギ等の栽培において強害雑草であるエ
キツクロア(Echinochloa、 ヒエ)属に効
果を示すものは、見いだされていない。
Upjiten Co., Ltd. (trade name), each of which has shown herbicidal effects against specific harmful weeds. However, nothing has been found to be effective against the genus Echinochloa, which is a harmful weed in the cultivation of rice, wheat, etc., which are important crops of the Poaceae family.

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

本発明は上述した様な現在の農作物生産の問題点を解決
するためのより有効な手段を提供するものである。すな
わち、イネ科作物に対する強害雑草を防除する病原微生
物、該病原微生物を含存する除草剤および雑草防除方法
を提供することを課題とする。。
The present invention provides a more effective means for solving the problems of current agricultural crop production as described above. That is, an object of the present invention is to provide a pathogenic microorganism that controls weeds harmful to grass crops, a herbicide containing the pathogenic microorganism, and a weed control method. .

[課題を解決するための手段] 本発明者らは、水田および畑地の重要雑草であるヒエの
防除を目的とし、エキツクロア(Echino−chl
oa、ヒエ)属に対する病原菌に注目し、多くの菌株を
探索、純粋分離し、その雑草防除効果を績討すると共に
他の作物、特にイネ、コムギに対する病原性の有無につ
いて検討し、米作、麦作においてヒエを防除することが
出来る新しい病原微生物を見出した。
[Means for Solving the Problems] The present inventors have developed Echino-chl.
Focusing on pathogenic bacteria for the genus A. oa and barnyard grass, we searched for and isolated many strains, evaluated their weed control effects, and investigated whether they are pathogenic to other crops, especially rice and wheat. We have discovered a new pathogenic microorganism that can control barnyard grass in wheat cultivation.

すなわち、水田の中に生育していて病徴を示しているヒ
エより、植物病原菌を分離するときに行なわれる通常の
方法によって病原微生物を純粋分離した。これらの分離
した多数の微生物の中からヒエに対して除草効果を示し
、イネに対して病害性及び寄生性を示さない病原菌を検
索し、本発明の病原微生物を見出し、本発明を完成した
That is, pathogenic microorganisms were purified and isolated from barnyard grass growing in rice fields and exhibiting disease symptoms using the usual method used to isolate plant pathogenic microorganisms. Among these many isolated microorganisms, we searched for pathogenic microorganisms that have a herbicidal effect on barnyard grass and are not disease-causing or parasitic on rice, and by discovering the pathogenic microorganism of the present invention, we have completed the present invention.

本発明はフザリウム オキシスポラム(Fusarju
+moxysporum) M H−0008(微工研
菌寄第10056号)新規病原微生物、該微生物含有す
ることを特徴とする雑草防除剤およびそれらによる雑草
防除方法に関する。
The present invention relates to Fusarium oxysporum (Fusarju).
+moxysporum) M H-0008 (Feikoken Bokujo No. 10056) relates to a novel pathogenic microorganism, a weed control agent characterized by containing the microorganism, and a weed control method using the same.

本発明に係わる病原微生物は、自然に生息する病徹を示
すヒエより簡単に分離でき、容易に大量培養が可能であ
り、効率的、かつ、大量に胞子を得ることができる0本
発明に係わる病原微生物は、好気性菌であり、生育可能
なpHは4〜8であり、好ましくはpH5〜6であり、
生育温度は15〜30℃、好ましくは23〜28℃であ
る6本発明に係わる病原性微生物は、ヒエに対し病原性
および防除効果を示し、イネ、食用ビニ、コムギ等のイ
ネ科作物、ナス、トマト等のナス科作物、ダイコン等の
アブラナ科作物、カポチャ等のウリ科作物に対しては、
定着性および病原性を示さず、ヒエに対し高い選択的防
除活性を示す。
The pathogenic microorganisms according to the present invention can be easily isolated from naturally occurring diseased barnyard grass, can be easily cultured in large quantities, and can efficiently obtain spores in large quantities. The pathogenic microorganism is an aerobic bacterium, and the pH at which it can grow is 4 to 8, preferably 5 to 6,
The growth temperature is 15 to 30°C, preferably 23 to 28°C.6 The pathogenic microorganism according to the present invention exhibits pathogenicity and control effects on barnyard grass, and is suitable for rice, edible wheat, grass crops such as wheat, and eggplant. For solanaceous crops such as tomatoes, cruciferous crops such as radish, and cucurbitaceous crops such as kapocha,
It exhibits no colonization or pathogenicity, and exhibits high selective control activity against barnyard grass.

〔実施例〕〔Example〕

以下に本発明に係わる病原微生物について実施例により
具体的に説明する。
The pathogenic microorganisms according to the present invention will be specifically explained below using Examples.

実施例1 1)病原微生物の分離方法 水田に自然発生し、病徴を示しているヒエを採取した。Example 1 1) Method for isolating pathogenic microorganisms Barnyard grass naturally occurring in paddy fields and exhibiting disease symptoms were collected.

病徴部分を中心として2〜3c′Ilの切片とし、70
%エタノール溶液に2〜3秒間浸漬後、2%次亜塩素酸
ナトリウム溶液に10分間浸漬することにより、ヒエの
表面を殺凹した。滅菌水で数回洗浄後、貧栄養平板培地
〔115ポテト・デクストロース寒天培地(以下PDA
培地と略す)、115チヤベツク寒天培地〕上に置き、
25℃の恒温器中で48〜72時間培養し、生育してき
た微生物を実体顕微鏡下で単菌糸分離し、病原微生物を
純粋分離した。得られた病原微生物は、ヒエに対する病
原性、定着性と殺草効果を検定し、更に、イネに対する
病原性及び定着性を検定し、ヒエに対して優れた殺草効
果を持ち、イネに対口で病原性及び定着性を示さない微
生物M H−0008を分離した。
Cut a section of 2 to 3 c'Il centered around the symptomatic area, and cut 70
% ethanol solution for 2 to 3 seconds, and then immersed in a 2% sodium hypochlorite solution for 10 minutes to kill the surface of the barnyard grass. After washing several times with sterile water, prepare an oligotrophic plate medium [115 potato dextrose agar medium (hereinafter referred to as PDA).
abbreviated as culture medium), placed on 115 Chabekku agar medium],
The microorganisms were cultured in a thermostat at 25° C. for 48 to 72 hours, and the grown microorganisms were separated into single hyphae under a stereomicroscope to isolate pure pathogenic microorganisms. The obtained pathogenic microorganisms were tested for pathogenicity, colonization, and herbicidal effect on barnyard grass, and were further tested for pathogenicity and colonization on rice. Microorganism MH-0008, which does not exhibit pathogenicity or colonization in the mouth, was isolated.

2)分離した微生物の同定 分離した微生物の同定は、微生物をPDA培地で培養し
、胞子の”形態や色素生産についてチエツクして行った
。その結果、M H−0008は、コロニーの色は白(
white)から薄い赤紫色(pale redν1o
let)あるいは白(white)からにふく光った赤
紫色(dull light red violet)
であり、マクロコニディア(macrocoa ld 
ia )とミクロコニディア(a+1croconid
ia)及び厚膜胞子を多数形成する。
2) Identification of the isolated microorganisms The isolated microorganisms were identified by culturing them in PDA medium and checking the spore morphology and pigment production. (
white) to pale red-purple (pale redν1o
or duel light red violet
and macroconidia (macrocoa ld)
ia ) and microconidia (a+1croconid
ia) and form large numbers of chlamydospores.

マクロコニディア(macroconidia)の太き
さおよびそれが隔壁を存した三日月型であることとミク
ロコニディア(microconidia)の大きさ及
び形状からフザリウム オキシスポラム(Fusari
um oxy−sporum)と判定された。
Based on the thickness of the macroconidia and its crescent-shaped shape with septa, and the size and shape of the microconidia, Fusarium oxysporum (Fusari
um oxy-sporum).

3)各培地における生育状況 PDA平板培地、ポテト・シェークロース寒天培地およ
びチャベック寒天培地における生育はいずれの培地でも
非常に良好である。25℃の恒温器中で5日間培養する
と、ペトリ皿(9cm )全体にひろがり、薄い紫色を
呈する。
3) Growth status on each medium Growth on PDA plate medium, potato shakerose agar medium, and Chavek agar medium is very good in all mediums. When cultured for 5 days in a 25°C incubator, it spreads over the entire Petri dish (9 cm) and takes on a light purple color.

4)生理学的性質 好気性菌であり、生育可能なpHは4〜8で、温度は1
5〜30’Cである。最適生育条件はpH5〜6、温度
23〜28°Cである。
4) Physiological properties It is an aerobic bacterium, and the pH at which it can grow is 4 to 8, and the temperature is 1.
5-30'C. Optimal growth conditions are pH 5-6 and temperature 23-28°C.

実施例2 大量培養法 本発明の病原微生物は、ジャーファーメンタでポテト・
デクストロース埼地(PD培地)を用いて温度25℃で
48時間培養することにより、2〜3と101胞子/d
となる。
Example 2 Large-scale cultivation method The pathogenic microorganism of the present invention was grown on potatoes in jar fermenta.
By culturing at 25°C for 48 hours using dextrose Saichi (PD medium), 2 to 3 and 101 spores/d were obtained.
becomes.

このように、本発明の病原微生物は大量培養により効率
的かつ大量に胞子を得ることができるため、微生物除草
側として使用可能である。
As described above, the pathogenic microorganism of the present invention can be used as a microorganism weed killer because spores can be obtained efficiently and in large quantities by mass culturing.

次に試験例によって本発明の病原微生物MH−0008
の優れた効果を具体的に説明する。
Next, according to test examples, the pathogenic microorganism MH-0008 of the present invention
The excellent effects of this will be explained in detail.

試験例1 ヒエを市販のポットで栽培し、およそ3〜4葉期の葉片
を用いて次に示す方法によって定着性の試験を実施した
Test Example 1 Japanese barnyard grass was cultivated in a commercially available pot, and a test for fixation was conducted using leaf pieces at approximately the 3rd to 4th leaf stage by the following method.

葉片を2%次亜塩素酸ナトリウム溶液中に10分間浸漬
したのち、滅菌水で十分に洗浄した。この葉片を十分に
無菌水を含ませた濾紙を敷いたプラスチックシャーレ中
に置いた。
The leaf pieces were immersed in a 2% sodium hypochlorite solution for 10 minutes, and then thoroughly washed with sterile water. The leaf pieces were placed in a plastic petri dish lined with filter paper soaked with sterile water.

一方、罹病葉から分離された病原微生物MH−0008
は、PDA培地で平板培養を行なった。培養した平板培
地より滅菌したコルクポーラ−により寒天を抜取り、こ
のディスクを無菌的にシャーレの中のヒエの葉片の上に
置き、25℃の恒温器中で72時間培養後、微生物のヒ
エに対する定着性を判定した。なお、比較対照として、
本発明の病原微生物M H−0008と同様の方法で分
離し、ヒエに対して病原性を存しない病原微生物(MH
−0007とM H−0010)を用いた。その結果を
表1に示した。
On the other hand, pathogenic microorganism MH-0008 isolated from diseased leaves
Plate culture was performed in PDA medium. Agar is extracted from the cultured plate medium using a sterilized cork polar plate, and this disk is placed on top of a leaf piece of barnyard grass in a petri dish aseptically. After culturing for 72 hours in a thermostat at 25°C, microorganisms colonize the barnyard grass. The sex was determined. For comparison,
A pathogenic microorganism (MH
-0007 and M H-0010) were used. The results are shown in Table 1.

表1 病原微生物のヒエに対する定着性病原微生物  
      定着性 M H−0008(本発明の病原微生物)++十MH−
0007(他の病原微生物)     −MH−001
0(他の病原微生物)    −(注)+++i葉の表
面で著しく増殖 ++;葉の表面で増殖 十 ;葉の表面でやや増殖 −;増殖せず 試験の結果、本発明の病原微生物M H−0008はヒ
エの表面で著しく増殖し、優れた定着性を示した。
Table 1 Pathogenic microorganisms that colonize barnyard grass
Colonization MH-0008 (pathogenic microorganism of the present invention) ++10MH-
0007 (Other pathogenic microorganisms) -MH-001
0 (Other pathogenic microorganisms) - (Note) +++i Significant growth on the leaf surface ++; Growth on the leaf surface 10; Slight growth on the leaf surface -; No growth Test results showed that the pathogenic microorganism of the present invention M H- 0008 significantly proliferated on the surface of barnyard grass and exhibited excellent fixation properties.

試験例2 ヒエを無菌的に試験管内で生育しく1.5葉期まで)、
試験材料とした。すなわち、種子を2%次亜塩素酸ナト
リウム溶液中に10分間浸漬したのち、滅菌水で十分に
洗浄した。この種子を、予め調製し滅菌したB5培地の
入った試験管に移植した。
Test Example 2 Aseptically growing barnyard grass in a test tube (up to the 1.5 leaf stage),
It was used as a test material. That is, the seeds were immersed in a 2% sodium hypochlorite solution for 10 minutes, and then thoroughly washed with sterilized water. The seeds were transplanted into test tubes containing previously prepared and sterilized B5 medium.

一方、分離した本発明の病原微生物M H−0008は
、PDA培地で平板培養を行なった。培養した平板培地
より滅菌したコルクポーラ−により寒天を抜取り、この
ディスクを無菌的に試験管内の中に置き、25℃の恒温
器中で120時間培養後、病原微生物のヒエに対する病
原性を判定した。その結果を表2に示した。
On the other hand, the isolated pathogenic microorganism MH-0008 of the present invention was plate cultured on a PDA medium. Agar was extracted from the cultured plate using a sterilized cork polar plate, and the disk was placed in a test tube aseptically and incubated in a thermostat at 25°C for 120 hours, after which the pathogenicity of the pathogenic microorganism to barnyard grass was determined. . The results are shown in Table 2.

表2 病原微生物のヒエに対する病原性病原微生物  
    病原性 M H−0008C本発明の病原微生物)++十MM−
0007(他の病原微生物)    −MH−0010
(他の病原微生物)    −(注)+++;ヒエが枯
死 ++;顕著な生育阻害 + ;やや生育阻害 −;影響なし 試験の結果、本発明の病原微生物M H−0008はヒ
エに対して優れた病原性を示した。
Table 2 Pathogenic microorganisms pathogenic to barnyard grass
Pathogenic MH-0008C Pathogenic microorganisms of the present invention) ++10MM-
0007 (Other pathogenic microorganisms) -MH-0010
(Other pathogenic microorganisms) - (Note) +++; Death of barnyard grass ++; Significant growth inhibition + ; Slight growth inhibition -; No effect As a result of the test, the pathogenic microorganism MH-0008 of the present invention was superior to barnyard grass. It showed pathogenicity.

試験例3 ヒエを市販のビニールポットで生育させ(1,5葉期)
、試験材料とした0本発明の病原微生物M H−000
8は、ポテトデキストロース液体培地(PD培地)で液
体培養を行なった。培養後培養液から胞子のみを得た。
Test Example 3 Growing barnyard grass in a commercially available vinyl pot (1st and 5th leaf stage)
, the pathogenic microorganism of the present invention M H-000 was used as a test material.
No. 8 was subjected to liquid culture in a potato dextrose liquid medium (PD medium). After culturing, only spores were obtained from the culture solution.

得られた胞子を0.05%ツイーン−80(Theen
−80)を含む水溶液中に懸濁し、ポットで栽培したヒ
エにスプレーし、温室内で25〜30℃で栽培してヒエ
の変化を観察した。接種量は1.5 X 10’、1.
5X10h、1.5 X 10’胞子/Idとし接種し
、2週間後のヒエの枯死の割合によって除草活性を調べ
た。その結果を表3に示した。
The obtained spores were mixed with 0.05% Tween-80 (Theen-80).
-80) was suspended in an aqueous solution and sprayed on barnyard grass grown in pots, and the mixture was grown in a greenhouse at 25 to 30°C to observe changes in the barnyard grass. The inoculation amount is 1.5 x 10', 1.
It was inoculated at 5 x 10 h and 1.5 x 10' spores/Id, and the herbicidal activity was examined by the percentage of death of barnyard grass two weeks later. The results are shown in Table 3.

表3 ヒエに対する防除活性 接種量(胞子/d)    防除率(%)1.5X10
’85 i、s x 1o”         to。
Table 3 Inoculum amount (spores/d) with control activity against barnyard grass Control rate (%) 1.5X10
'85 i,s x 1o'' to.

1.5 X 10’         100試験の結
果、本発明のM H−0008はヒエに対して優れた除
草効果を示した。
As a result of the 1.5 x 10' 100 test, MH-0008 of the present invention showed an excellent herbicidal effect on barnyard grass.

次に、本発明の病原微生物M H−0008の作物に対
する病原性及び定着性について検討を行い、本発明の病
原微生物M H−0008が作物に対する病害の発生が
無い病原微生物であることを確認した。
Next, we investigated the pathogenicity and colonization of the pathogenic microorganism MH-0008 of the present invention on crops, and confirmed that the pathogenic microorganism MH-0008 of the present invention is a pathogenic microorganism that does not cause disease on crops. .

試験例4 病原性については試験例3で示したと同様の方法で行い
、定着性については試験例1の方法に従って行った。ヒ
エ以外の植物体としては、イネ(日本晴、ササニシキ)
、食用ビニ(パニカム属)、コムギ、ナス、トマト、ダ
イコン、カポチャについて実施した。その結果を、表4
に示した。
Test Example 4 Pathogenicity was tested in the same manner as in Test Example 3, and fixation was tested in accordance with the method in Test Example 1. Plants other than barnyard grass include rice (Nipponbare, Sasanishiki)
, edible beetles (Panicum spp.), wheat, eggplant, tomatoes, radish, and kapocha. The results are shown in Table 4.
It was shown to.

試験の結果、本発明の病原微生物M H−0008はイ
ネ(日本晴、ササニシキ)、食用ビニ(バニカム属)、
コムギ、ナス、トマト、ダイコン、カポチャに対して、
病原性および定着性を示さなかった。
As a result of the test, the pathogenic microorganism MH-0008 of the present invention was found to be effective in rice (Nipponbare, Sasanishiki), edible rice (Banicum sp.),
For wheat, eggplant, tomato, radish, kapocha,
It showed no pathogenicity or colonization.

表4 作物に対する本発明病原微生物のの反応性作物 
    病原性     定着性イネ 日本晴     −− ササニシキ   −− 食用ヒエ     −− コムギ      −       −ナス     
  −− トマト      −− ダイコン     −− カポチャ     −− 〔発明の効果〕 本発明の病原微生物フザリウム オキシスポラム(Fu
sarium oxysporum) M H−000
8(微工研菌寄第10056)はヒエに対して選択的に
病原性及び定着性を示し、この微生物の胞子を用いると
、他の作物や植物体に影響を与えることなく、また、化
学合成農薬の様に施用時期の限定が少なく、イネの強害
雑草であるヒエを防除することが出来る。
Table 4 Reactivity of the pathogenic microorganism of the present invention to crops
Pathogenicity Fixed rice Nipponbare −− Sasanishiki −− Edible barnyard grass −− Wheat − −Eggplant
-- Tomato -- Radish -- Kapocha -- [Effects of the Invention] The pathogenic microorganism Fusarium oxysporum (Fu
sarium oxysporum) M H-000
8 (Feikoken Bacteria No. 10056) exhibits selective pathogenicity and colonization properties for barnyard grass, and when the spores of this microorganism are used, they can be used to chemically control plants without affecting other crops or plants. Unlike synthetic pesticides, there are fewer restrictions on the timing of application, and it can control barnyard grass, which is a harmful weed to rice.

さらに、本発明の病原微生物M H−0008は、天然
に存在する微生物の中から選択されたものであり、化学
合成農薬で懸念される環境汚染の心配な(、安全に使用
出来る。
Furthermore, the pathogenic microorganism MH-0008 of the present invention is selected from naturally occurring microorganisms and can be used safely without the environmental pollution concerns associated with chemically synthesized pesticides.

Claims (3)

【特許請求の範囲】[Claims] (1)フザリウムオキシスポラム(Fusariumo
xysporum)MH−0008(微工研菌寄第10
056号)新規病原微生物。
(1) Fusarium oxysporum (Fusarium oxysporum)
xysporum) MH-0008 (Microtechnical Laboratory No. 10
No. 056) Novel pathogenic microorganism.
(2)フザリウムオキシスポラム(Fusariumo
xysporum)MH−0008(微工研菌寄第10
056号)新規病原微生物を含有することを特徴とする
雑草防除剤。
(2) Fusarium oxysporum
xysporum) MH-0008 (Microtechnical Laboratory No. 10
No. 056) A weed control agent characterized by containing a novel pathogenic microorganism.
(3)フザリウムオキシスポラム(Fusariumo
xysporum)MH−0008(微工研菌寄第10
056号)新規病原微生物を用いる雑草防除方法。
(3) Fusarium oxysporum
xysporum) MH-0008 (Microtechnical Laboratory No. 10
No. 056) Weed control method using novel pathogenic microorganisms.
JP63162592A 1988-07-01 1988-07-01 Novel pathogenic microorganisms, herbicides containing the microorganisms, and weed control methods using them Pending JPH0213367A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63162592A JPH0213367A (en) 1988-07-01 1988-07-01 Novel pathogenic microorganisms, herbicides containing the microorganisms, and weed control methods using them

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63162592A JPH0213367A (en) 1988-07-01 1988-07-01 Novel pathogenic microorganisms, herbicides containing the microorganisms, and weed control methods using them

Publications (1)

Publication Number Publication Date
JPH0213367A true JPH0213367A (en) 1990-01-17

Family

ID=15757520

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63162592A Pending JPH0213367A (en) 1988-07-01 1988-07-01 Novel pathogenic microorganisms, herbicides containing the microorganisms, and weed control methods using them

Country Status (1)

Country Link
JP (1) JPH0213367A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993005656A1 (en) * 1991-09-17 1993-04-01 Japan Tobacco Inc. Novel microorganism, weedkiller containing same, and weed control by using same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993005656A1 (en) * 1991-09-17 1993-04-01 Japan Tobacco Inc. Novel microorganism, weedkiller containing same, and weed control by using same
US5434120A (en) * 1991-09-17 1995-07-18 Japan Tobacco Inc. Ustilago trichophora mycoherbicidal compositions and methods of use

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