CN1685833A - Application of blue mould in preventing and treating plant soil infected disease - Google Patents

Application of blue mould in preventing and treating plant soil infected disease Download PDF

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CN1685833A
CN1685833A CNA2005100389792A CN200510038979A CN1685833A CN 1685833 A CN1685833 A CN 1685833A CN A2005100389792 A CNA2005100389792 A CN A2005100389792A CN 200510038979 A CN200510038979 A CN 200510038979A CN 1685833 A CN1685833 A CN 1685833A
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mould
solid
plant soil
borne diseases
phytophthora
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CN1270610C (en
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马艳
常志州
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Jiangsu Academy of Agricultural Sciences
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Jiangsu Academy of Agricultural Sciences
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Abstract

An application of penicillium striatisporum in preventing and treating the soil-transmitted diseases of plant features that its solid, or the mixture of it and organic fertilizer, or its metabolism product in its liquid culture medium is applied to the root of plant.

Description

The application of a kind of mould in the plant soil-borne diseases control
Technical field
The present invention relates to the application of a kind of mould in the plant soil-borne diseases control, specifically is a kind of application of mould penicillium striatisporum in the plant soil-borne diseases control that disease funguses such as Phytophthora is had strong antagonism.Belong to and utilize microorganism that corps diseases is carried out the biological control field.
Background technology
In the multiple diseases of plant, the difficulty of prevention and cure maximum of soil-borne disease.Because it is more that airborne pathogen is subjected to air humidity, temperature, ultraviolet influence, quantity and pathogenic on be subjected to the influence of environment easily and weakened, in facility cultivation, can wet by temperature control, control and artificially regulate the generation that these factors prevented or alleviated disease especially; And soil is a metastable ecotope, ring also less relatively so the pathogen in the soil is subjected to extraneous secondary face, the method and the approach of artificial control are also very limited, thereby the invalid body in the soil can survive and reach more than ten years, make soil-borne disease become the persistent ailment of plant disease.In soil-borne disease, pathogen is infected from seed or the root system of plant, and the preventive effect of overground part is very little or absolutely void, so in case crop is susceptible, does not just have and can save, this point difficulty of prevention and cure more susceptible than above-ground plant parts obviously strengthens.
Separately carrying out the main difficult problem that the control of soil-borne disease runs into the biological and ecological methods to prevent plant disease, pests, and erosion microorganism is the effect instability, its reason is a lot, thereby but main cause just is that the biocontrol bacterial strain that external source applies can not the very fast this advantage of maintenance that occupies advantage and long period in root colonization, propagation on nutrition and space.Fertilizer owing to have improves rhizosphere environment, provides balanced nutrient, the nutrition condition of improving plant, the field planting that promotes plant root, the function of growth for plant, in agricultural production, used for a long time as base manure always, yet, even in a large amount of little territories of the general fertilizer of executing specific to the plant rhizosphere, its amount is also still limited, does not satisfy the nutritional condition of the interior recovery needs of biocontrol microorganisms short time that root applies; Particularly under the facility cultivation condition, long-term high temperature, high humidity, high fertilizer, continuous cropping, continuous cropping cause soil quality seriously to descend, nutrition is unbalanced even deficient, the habitat that not only is difficult to after biocontrol bacterial strain applies separately obtain suiting is grown fast, is bred, and dead at short notice owing to the adverse circumstances of incompatibility root soil probably.
In the biological control of plant disease research and use more microorganism mainly to have: the bacterium class, as had no pathogenicity agrobacterium, erwinia, bacillus, pseudomonad etc.; Actinomycetes mainly contain streptomyces hygroscopicus etc.; Mycophyta has the Trichoderma harzianum of trichoderma, healthy and free from worry wood mould etc., saprophytic property, pythium spp, thick spore Verticillium dahliae and avirulent sickle-like bacteria, rhizoctonia etc.Compare with the application of other microorganisms on control of plant disease, particularly research, the application report of soil-borne disease biological control is less relatively in plant disease about Penicillium notatum, external research report mainly contains following several: (1) penicillium purpurogenum, Melgarejo﹠amp; The penicillium purpurogenum that M-Sagasta.I (Melgarejo, 1984) is separated to from peach branch can produce digestive enzyme and destroy the hyphal cell of pathogen and the fusarium wilt that sickle-like bacteria Fusarium oxysporum causes is played protection effect; (2) penicillium frequentans, the sour rot that the antagonistic substance that M-Sagasta.I (1986) research report mould penicilliumfrequentans produces can be prevented and treated the fruit that is caused by Geotrichum candidum; Antonieta De Cal (Antonieta De Cal, 1988) report mould penicillium frequentans liquid state leaves standstill to cultivate has two kinds of antagonistic substances to produce after 10 days, generation is the highest after 20 days, antibiosis is active after 30 days descends, shaking table is cultivated no antagonistic substance, the antagonistic substance that produces is to Monilinia laxa., wood is mould, mould, sickle-like bacteria, 14 kinds of fungies such as grey mold have antibiosis, can prevent and treat the brown rot of the drupe class crop that causes by this Monilinia laxa., and the antagonistic substance that produces carried out separation and purification, but to the mould no antibiosis phenomenon of epidemic disease; The growth conditions that Susan pascual (Susan pascual, 2000) has studied this mould penicillium frequentans produces antagonistic substance to its metabolism and to the influence of Monilinia laxa preventive effect; (3) penicillium funiculosum, Fang JG (Fang JG, 1995) research has reported that mould penicillium funiculosum is mould to phytophthora parasitica, oranges and tangerines brown rot epidemic disease, the biological and ecological methods to prevent plant disease, pests, and erosion mechanism of the root rot of the camphor tree epidemic disease mould azalea that causes and oranges and tangerines mainly contains the mycelia that penetrates, degrades, and produces the growth that antagonistic substance suppresses the phytophthora root rot primordial hypha; Pathogens such as also mould to corruption, upright withered, reaping hook, big beautiful Verticillium dahliae have antagonism, research is also found in the matrix pot experiment, the protection effect of the solid fungicide that adding wheat bran solid culture generates is than effective with spore suspension filling root separately, reason is that the wheat bran in the solid fungicide provides nutrition for the growth of biocontrol microorganisms, and therefore research pointed out should consider in biological control with biological and ecological methods to prevent plant disease, pests, and erosion microorganism and the use of proper nutrition material compatibility.(4) penicillium oxalicum penicillium oxalicum, Gintis.B.O. (Gintis.B.O.1987) report that it prevents and treats the mould azalea root-rot disease that causes of epidemic disease by producing antagonistic substance; Walter J. (Walter J., 1984) report penicillium oxalicum can be prevented and treated the mould young beans damping off that causes of ultimate corruption; The main Biocontrol Mechanism of report penicillium oxalicums such as I.Larena is not by producing digestive enzyme such as pectase but prevents and treats the microbial fusarium wilt of reaping hook (Antonieta De Cal, 1995,1997,1999 by inducing plant to produce resistance; Susanpascual, 1997; I.Larena, 2002), and carried out in this respect deeply, systematic research: make seed afterbirth, seedling stage root on the vegetables such as pea, tomato and insert indoor and field experiments such as conidium, and to the growth characteristics of penicillium oxalicum, in the ecologic competition power of plant rhizosphere, carried out deep research with captan or metalaxyl compatibility operating position, best product spore condition of culture and the preservation characteristic of spore microbial inoculum and condition of suitability for industrialized production etc.Domestic, the Wu Lidong report can be prevented and treated shirt wood sprout term disease (Wu Lidong, 1994) with penicillin; Ceng Jinfeng report mould Z-88 bacterial strain has antibiosis to Rhizoctonia solani Kuhn and to rice seed germination facilitation (Ceng Jinfeng, 1995).The pectase that the indoor by experiment research of Peng Xiawei report penicillium oxalicum produces can inducing cucumber to the resistance of scab Cladosporium cucumerinum.
Because Penicillium notatum is a big class fungi microbe that extensively exists, of a great variety, majority is a saprophytic bacteria.The minority kind of Penicillium notatum can infect fruit and cause brown rot or penicilliosis; The kind that has is the important economic worth fungi of industry and medicine, produce penicillin as penicillium chrysogenum Penicillium chrysogenum Thom, for rescue human life and social development make a great contribution, remain one of effective and safe antibiotics that industries such as medical treatment, feed mainly use now; The kind that has can produce phytase, zytase, lipase, amylase, carotin, microbial flocculant etc., has been widely used in the industrial fermentation industry, produces huge economic benefit.In addition, compare with bacterium, the Penicillium notatum condition of culture is various, and solid-state, liquid training method can both be used, and is easy to cultivate; And simple to nutritional requirement, the offcuts in agricultural byproducts or the industrial production all are the good medium of cultivating Penicillium notatum as wheat bran, rice bran, blackstrap, wide material sources are cheap; Growth, reproduction speed is fast, and it is strong to produce the spore ability, and environmental suitability is preferably arranged, and these characteristics are for suitability for industrialized production in the future and use very favourable.
The Jiangsu Province Agriculture Science Institute obtains a kind of mould from the plant rhizosphere screening, is accredited as penicillium striatisporum through Chinese agriculture microorganism fungus kind preservation center.Strain characteristics is: bacteria colony white, cushion on the PDA medium, and hyphae colorless, 0.8-1.4 μ m is wide; Conidiophore is short, column has branch sometimes, generally long 5-15 μ m, be no more than 30 μ m, wide 1.0-1.5 μ m, many 3-5 on bottle stalk is born in the conidiophore top, and idol has singly is born in mycelia or conidiophore side, 3.1-7.1 * 1.6-2.8 μ m, the flask shape, nearly base portion is the wideest, top wide 0.5-1.2 μ m; Conidium is oval to subcircular, circle, concatenates on the bottle stalk, and tangible connector is arranged between the spore; Ripe spore surface is coarse, visible significantly 3-several from line, 2.5-2.9 * 2.1-2.5 μ m.
Mould penicillium striatisporum separated acquisition in 1969 by Stolk A C at first from Turkey's soil, Index Fungorm database is classified this kind as the different name of Penicillium restrictum, but the mould penicillium striatisporum that relates among the present invention is undertaken finding that ribosome between the Penicillium restrictum in this mould penicillium striatisporum bacterial strain and the database-DNA ITS region sequence similitude is not high when bacterial classification is identified by Chinese agriculture microorganism fungus kind preservation center.
The domestic application in the research in biological control field for mould carried out lessly, yet there are no the report that relevant mould penicillium striatisporum bacterial strain is particularly used on the soil-borne disease in controlling plant diseases especially at present both at home and abroad.
Summary of the invention
The objective of the invention is to: bigger at difficulty in the soil-borne disease control of plant, the habitat that not only is difficult to obtain suiting after using microorganisms such as more bacterium class, actinomycetes to apply is at present grown fast, is bred, and dead at short notice owing to the adverse circumstances of incompatibility root soil probably, directly have influence on the control efficiency of these microorganisms to soil-borne disease.Proposition is wider with a kind of antimicrobial spectrum, and growth rate is very fast, is easy to cultivate, and the mould penicillium striatisporum that rhizosphere field planting power is strong is applied in the soil-borne disease control of plant.
The object of the present invention is achieved like this: the application of a kind of mould in the plant soil-borne diseases control is characterized in that: with the form control plant soil-borne diseases of mould penicillium striatisporum with the liquid culture metabolite of solid fungicide form, solid fungicide and solid organic fertilizer compatibility form and this mould.
Described mould penicillium striatisporum solid fungicide is to obtain like this: with the preservation bacterial classification of mould penicillium striatisporum insert carry out the test tube slant activation in the test tube slant medium after, inserting the capacity that liquid nutrient medium is housed again is the triangular flask of 250ml, and liquid amount is 80ml/250ml; Place shaking table to cultivate 3-4 days triangular flask, the rotating speed 160r/min of shaking table, the environmental temperature of culture period is 28 ± 2 ℃; Finish the back and in 28 ± 2 ℃ of environment, continue to cultivate 6-8 days, turned once every 2-3 days, to producing spore with 5% inoculum concentration (V/W) access solid culture medium; Pulverized the 10-20 mesh sieve after last natural air drying or 30 ℃ of oven dry, and obtained solid fungicide, the bacteria containing amount in the solid fungicide is 10 10-11Cfu/g.
In the process that obtains mould penicillium striatisporum solid fungicide, described test tube slant medium is: glucose 10 grams, peptone 5 grams, KH 2PO 41 gram, MgSO 47H 2The O0.5 gram, agar 15-20 gram, pH nature, 1000 milliliters in water; Described liquid nutrient medium is: glucose 10 grams, peptone 5 grams, KH 2PO 41 gram, MgSO 47H 2O 0.5 gram, pH nature, 1000 milliliters in water; Described solid culture medium is: wheat bran, the peat composed of rotten mosses, vermiculite, their quality proportioning is 1: 3: 1.
Described liquid culture metabolite is to obtain like this: with the preservation bacterial classification of mould penicilliumstriatisporum insert carry out the test tube slant activation in the test tube slant medium after, inserting the capacity that liquid fermentation medium is housed again is the triangular flask of 250ml, and liquid amount is 80ml/250ml; The rotating speed 160r/min of shaking table, the environmental temperature of culture period is 28 ± 2 ℃; After placing shaking table to cultivate 6-8 days the triangular flask, two-layer filtered through gauze is gone out mycelia, collects filtrate and is the liquid culture metabolite through the bacteria-free filtrate of the miillpore filter preparation of 0.45 micron of diameter.
In the process that obtains mould penicillium striatisporum liquid culture metabolite, described liquid fermentation medium is preparation like this: take by weighing potato 200 grams, peeling, be cut into piece and boil half an hour, use two-layer filtered through gauze then, add glucose 20 gram again, supply water to 1000 milliliter after dissolving, 121 ℃ of autoclavings 20 minutes obtain liquid fermentation medium.
With solid fungicide form control plant soil-borne diseases is to spread manuer in holes in crop root part after solid fungicide is mixed thoroughly with 5-8 times of vegetable garden soil, and every cave contains solid fungicide 0.1-0.3 gram, or is 1 with solid fungicide with the native weight proportion of growing seedlings, and: 200-500 mixes and afterwards adorns alms bowl and grow seedlings; Solid fungicide and solid organic fertilizer compatibility form control plant soil-borne diseases is to be 1 with solid fungicide with solid organic fertilizer compatibility weight proportion: spread manuer in holes after 50-100 mixes in the plant root, the 15-20 that whenever spreads manuer in holes restrains; Described liquid culture metabolite form control plant soil-borne diseases is that the liquid culture metabolite is used for the root pouring or is sprayed on plant after doubly with the Tween-20 dilution 100-200 of 0.05-0.1%, and every strain irrigation amount was a 20-50 milliliter dilution when wherein root watered.
Described solid organic fertilizer be agricultural solid residue through biofermentation, deodorization, dewater, through the fertilizer of the back formation of becoming thoroughly decomposed.Agricultural solid residue comprises: various offcuts and waste that the deep development of feces of livestock and poultry, agricultural crop straw, primary agricultural products brings.
The eqpidemic disease that described soil-borne disease refers to cause by soilborne Phytophthora, Sclerotinia, Rhizoctonia, pythium disease fungus, stalk break, damping off, banded sclerotial blight, damping off etc.Wherein, the Phytophthora disease fungus comprises: Phytophthora capsici Phytophthora capsici Leonian, phytophthora infestans Phytophthora infestans de Bary, soybean phytophthora Phytophthora megaspermaDrecgsler, epidemic diseases such as Phytophthora nicotianae Phytophthora nicotianae Breda Hann, the mould Phytophthora drechsleri of Jue Shi epidemic disease Tucker are mould; Described Sclerotinia disease fungus comprises: Sclerotinia sclerotiorum Sclerotinia sclerotonium; Described Rhizoctonia disease fungus comprises: Rhizoctonia solani Kuhn Rhizoctonia solani Kuhn, cereal rhizoctonia Rhizoctonia Van der Hoeven etc.; Described pythium disease fungus comprises: the rotten mould Pythium aphanidermatum of melon and fruit, the mould Pythium ultimum of ultimate corruption etc.
The invention has the advantages that: owing to adopt mould penicillium striatisporum is the core bacterial strain, not only growth rate is very fast, be easy to cultivate, rhizosphere field planting power is strong, and disease funguses such as eqpidemic disease, stalk break, damping off, banded sclerotial blight, damping off are had strong antagonism; This bacterial strain has a clear superiority in than other penicillium bacterial strains of having reported both at home and abroad, and antagonistic substance simple and convenient extraction, the result of initial gross separation, purifying shows that the antagonistic substance that this penicillium bacterial strain produces is the non-albumen micromolecular of a 2-3 kind antibiotic, high temperature resistant preferably, acid and alkali-resistance, UV resistant performance are arranged, handled 30 minutes for 80 ℃, activity still keeps 80%, and each component all has activity separately, there is not dependence each other, promptly has the various active form, and can be dissolved in the multiple organic solvent, help antibiotic product development; The production of this mould solid fungicide adopts conventional solid tray to cultivate, and cost is low, and production method is simple, and is workable; Using method is versatile and flexible, both solid fungicide directly can be spreaded manuer in holes, again can solid fungicide and the compatibility of fertilizer use, result of use is all very stable; New force is injected by the present invention preventing microorganism family of making a living, and a kind of new living resources are provided.
Embodiment
Embodiment 1:a) culture medium preparation of cultivation mould penicillium striatisporum solid fungicide
Test tube slant culture medium preparation: take by weighing: glucose 10 grams, peptone 5 grams, KH 2PO 41 gram, MgSO 47H 2O 0.5 gram, be dissolved in 1000 ml waters, add agar 15-20 gram, heating is boiled to agar and is dissolved, and supplies volume to 1000 milliliter, suitably cooling back branch installs in the test tube, loading amount is the 1/5-1/6 of test tube height, with the good test tube mouth of test tube plug plug, 121 ℃ of autoclaving 25min, it is standby to cooling off to take out pendulum inclined-plane, back while hot, and bevel altitude is no more than 1/3 of test tube height.
The preparation of liquid seed culture medium: take by weighing glucose 10 grams, peptone 5 grams, KH 2PO 41 gram, MgSO 47H 2O 0.5 gram is dissolved in 1000 ml waters, packing then, and liquid amount is the 80-100ml/250ml triangular flask, with the good bottleneck of tampon plug, 121 ℃ of autoclaving 25min, the cooling back is standby.
The preparation of solid culture medium: get: wheat bran, the peat composed of rotten mosses, vermiculite, their quality proportioning is 1: 3: 1.In the present embodiment, get wheat bran 1kg, peat composed of rotten mosses 3kg, vermiculite 1kg evenly stir, and adding water, to adjust the medium moisture be 60-65%, and 121 ℃ of autoclaving 40min sterilized once at similarity condition in second day again, and the cooling back is standby.
B) preparation of the liquid fermentation medium of the liquid culture metabolite of cultivation mould penicillium striatisporum
The preparation of liquid fermentation medium: claim potato 200 grams, peeling is cut into piece and is boiled half an hour, uses two-layer filtered through gauze then, adds glucose 20 grams again, supplies water to 1000 milliliter after dissolving, and 121 ℃ of autoclavings 20 minutes are standby.
Embodiment 2: the preparation of mould penicillium striatisporum solid fungicide
The mould penicillium striatisporum that the present invention relates to is obtained from the plant rhizosphere screening by the Jiangsu Province Agriculture Science Institute, and adopts slant preservation bacterial classification or ampoul tube lyophil preservation bacterial classification.
A) activation of bacterial classification
Adopt the activation method of slant preservation bacterial classification: the bacterial classification inoculation about diameter 8mm of picking in the bacterial classification of slant preservation is activated, in 28 ± 2 ℃ environment, cultivate after 3-5 days standby in the test tube slant medium.
Adopt the activation method of ampoul tube lyophil preservation bacterial classification: in superclean bench, clean ampoule with 70% cotton ball soaked in alcohol, in ampoule, frustrate ditch one with emery wheel then, wrap ampoule with sterile gauze pad or sterile towel, break ampoule into two with one's hands with hand then, to wherein adding the 0.5-1.0ml liquid nutrient medium, slowly rotate ampoule, make the freeze-drying lactobacillus rehydration, and then this is transferred in the test tube slant medium activates, in 28 ± 2 ℃ environment, cultivate after 3-5 days standby.
B) liquid culture
It is being equipped with in the 83.3ml liquid nutrient medium triangular flask of 250ml that bacterium piece about three diameter 8mm of mould picking that test tube is activated is seeded in three volumes respectively, place shaking table, the rotating speed 160r/min of shaking table continues to cultivate in 28 ± 2 ℃ environment, cultivates standby after 3-4 days.
C) solid culture
The 250ml bacterial classification of liquid culture is inserted in the 5kg solid culture medium, solid culture is tiled in the tray, thickness 5-8cm, the double-deck gauze of handling through autoclaving on the upper cover, in 28 ± 2 ℃ of environment, continue to cultivate 6-8 days, turned once every 2-3 days, suitably add sterile water simultaneously, be cultured to the product spore; Last natural air drying or 30 ℃ of oven dry (moisture is less than 10%) are solid fungicide, and the microbial inoculum bacteria containing amount is 10 10-11Cfu/g.
More than all inoculation operations must be under aseptic condition, promptly other or handle 1-2 hour room through ultraviolet disinfection at the alcolhol burner of superclean bench, the room of solid culture also needs to handle 1-2 hour with ultraviolet disinfection in advance.
Embodiment 3: the use of mould penicillium striatisporum solid fungicide
Contain mould penicillium striatisporum solid fungicide, can use on the seedbed: is 1 with the soil of growing seedlings with weight ratio with the solid fungicide that the present invention relates to: 200-500 mixes the back and adorns alms bowl and grow seedlings, and can reach 40-70% to the preventive effect of seedbed soil-borne disease.
The solid fungicide that contains mould penicillium striatisporum can also use when transplanting: before planting seedling, spread manuer in holes after mixing thoroughly with 5-8 times of vegetable garden soil during use, every cave contains solid fungicide 0.1-0.3 gram.
Embodiment 4: when the bacterial manure of mould penicillium striatisporum solid fungicide and fertilizer compatibility used, fertilizer was to the synergistic effect of penicillium bacterial strain at rhizosphere colonization
Solid fungicide with mould penicillium striatisporum is the bacterial manure that mixes at 1: 80 with the compatibility weight proportion of solid organic fertilizer, carries out the potted plant test of spreading manuer in holes, and potted plant is to use behind the vegetable garden soil natural air drying with soil.When capsicum was transplanted, every strain 15-20 gram was spreaded manuer in holes bacterial manure than using the equivalent microbial inoculum separately and is obviously helped the field planting (see Table 1) of mould at rhizosphere.Transplant after 20 days, execute the processing of bacterial manure, the quantity of capsicum rhizosphere Penicillium notatum is to use 14.3 times of equivalent microbial inoculum separately, and the former Penicillium notatum shared ratio in the rhizosphere fungi also is higher than the latter far away, becomes the dominant microflora in the fungi.Transplanted back 40 days, Penicillium notatum still has 2.5 * 10 in the quantity of rhizosphere 5The cfu/g dry ground accounts for 73% of rhizosphere total number of fungi, and the ability of the very strong rhizosphere colonization and the population of keeping on top is arranged.
Table 1 fertilizer is to the synergistic effect (unit: (* 10 of penicillium bacterial strain at rhizosphere colonization 5The cfu/g dry ground))
20 days 40 days processing time Blank Fertilizer Penicillium notatum Bacterial manure
Mould accounts for fungi total bacteria count proportional numbers (%) 0000 Mould accounts for fungi total bacteria count proportional numbers (%) 0000 Penicillium notatum accounts for total number of fungi and counts ratio (%) 0.752 13.6 0.655 26 Mould accounts for fungi total bacteria count proportional numbers (%) 10.7 96 2.5 73
Embodiment 5: the bacterial manure of mould penicillium striatisporum solid fungicide and solid organic fertilizer compatibility uses the sick preventive effect of Phytophthora capsici (producing the booth test)
The bacterial manure that mixes with the compatibility of solid organic fertilizer with the solid fungicide of mould penicillium striatisporum, produce the booth test, before the test, select sub-district 1, sub-district 2, sub-district 3 and sub-district 4 as practice ground, experiment is with capsicum variety: Soviet Union green pepper No. 2.In above-mentioned sub-district: sub-district 1, sub-district 2 are organized in contrast, adopt conventional cultivation, the carbendazim of spreading manuer in holes during transplanting, and amount of application is: 0.2-0.5 gram/cave+equivalent fertilizer; Sub-district 3, sub-district 4 adopt bacterial manure to handle as the experimental group of bacterial manure, during transplanting, and the bacterial manure of the 15-20 that spreads manuer in holes gram, mould penicilliumstriatisporum solid fungicide and solid organic fertilizer weight proportion are 1: 70 in the described bacterial manure.
This bacterial manure of spreading manuer in holes when capsicum is transplanted can obviously promote the growth of capsicum, and significantly better than contrast (seeing Table 3), single output increases by 37.3% on the indexs such as transplanting back 20 days, 40 days, the plant height of capsicum, stem were thick, the number of sheets, leaf are wide, fruit number and degree of development; Transplanting 40 days, sub-district 1 and sub-district 2 have 38 strains and fall ill because of Phytophthora capsici Phytophthora capsici Leonian, and promptly the control group incidence of disease is about 18.36%, handle through the bacterial manure of spreading manuer in holes, 1 strain morbidity is only arranged the same period, and promptly the experimental group incidence of disease only is 0.47% (seeing Table 2); In addition, all observe the processing of the bacterial manure of spreading manuer in holes in potted plant and booth test, the capsicum seedling-slowing stage obviously shortens 4-5 days than the contrast of executing equivalent microbial inoculum or fertilizer separately, illustrates that this bacterial manure can promote growing of root system.
The investigation of table 2 incidence
Project is handled 10 days 20 days 40 days 60 days The strain number Output (jin) Output (jin /)
Contrast contrast bacterial manure bacterial manure 3 sub-districts 4,2 sub-districts, 1 sub-district, sub-district ??0 ??0 ??0 ??0 ??0 ??0 ??0 ??0 ??22 ??16 ??0 ??1 ??0 ??0 ??0 ??0 ??103 ??104 ??99 ??112 ??75.6 ??70.5 ??102 ??103.5 ??0.73 ??0.68 ??1.03 ??0.92
Table 3 is transplanted back growing way investigation in 20,40 days
Project is handled Plant height (centimetre) Stem thick (centimetre) The number of sheets (sheet) Leaf wide (centimetre) 40 days
20 days 40 days 20 days 40 days 20 days 40 days 20 days 40 days Number of results (individual) Degree of development (cm)
The fertile medicine fertilizer of contrast contrast medicine 3 sub-districts 4,2 sub-districts, 1 sub-district, sub-district ?41.9 ?41.6 ?53.6 ?50.5 ?51.6 ?45 ?58.6 ?51.4 ?0.96 ?1.18 ?1.16 ?1.26 ?1.02 ?1.3 ?1.3 ?1.32 ?36.4 ?32.1 ?61 ?54.8 ?50.6 ?44.1 ?69.8 ?59.2 ?3.1 ?3.6 ?3.74 ?3.66 ?3.9 ?3.92 ?3.88 ?3.78 ?16 ?20 ?29 ?25 ?45.2 ?41.2 ?53.6 ?47.4
Embodiment 6: mould penicillium striatisporum is to the antibiosis of Sclerotinia sclerotiorum
A) mould penicillium striatisporum bacterial strain is to the dull and stereotyped antagonism of Sclerotinia sclerotiorum
Mould penicillium striatisporum bacterial strain is at the mycelial growth that suppresses the former bacterium of sclerotinia rot of colza on the flat board consumingly: behind the synchronous inoculated and cultured 4-5d of the former bacterium of Penicillium notatum and sclerotinia rot of colza, can not grow mould periphery of bacterial colonies pathogen mycelia, the antagonism band of a width for about 13-15mm arranged, and dull and stereotyped other local pathogen mycelia energy normal growth shows that the Penicillium notatum metabolite has tangible antagonism to the former bacterium of sclerotinia rot of colza.
B) mould penicillium striatisporum strain liquid is cultivated the influence of metabolite to Sclerotinia sclerotiorum hyphal cell structure
The sclerotium germ mycelia piece that microexamination is handled through penicillium bacterial strain liquid culture metabolite shows: the hyphal cell wall still is kept perfectly, but protoplasm homogeneous transparent no longer in the cell, but being condensed into many particulate materials, the cell interior structure is destroyed; The pathogen inoculated by hypha block of handling is cultivated on the PDA flat board, do not see mycelial growth; With the pathogen inoculated by hypha block of the handling cultivation of on the rape leaf of falling 1-2, preserving moisture, be contrast to inoculate normal pathogen mycelia piece, after 6 days, to handle and scab do not occur, tangible scab has appearred in contrast; After 8 days, the contrast scab continues to increase, and does not occur scab yet and handle.Antagonistic substance in the possible culturing filtrate kills the hyphal cell of Sclerotinia sclerotiorum by destroying cell structure, and it is pathogenic that it is completely lost.
Embodiment 7: the cultivation of liquid culture metabolite
Claim potato 200 grams, peeling is cut into piece and is boiled half an hour, uses two-layer filtered through gauze then, adds glucose 20 grams again, supplies water to 1000 milliliter after dissolving, and 121 ℃ of autoclavings 20 minutes obtain liquid fermentation medium.
With the preservation bacterial classification of mould penicillium striatisporum insert carry out test tube slant activation in the test tube slant medium after, inserting the capacity that liquid fermentation medium is housed again is the triangular flask of 250ml, liquid amount is 80ml/250ml; The rotating speed 160r/min of shaking table, the environmental temperature of culture period is 28 ± 2 ℃; After placing shaking table to cultivate 6-8 days the triangular flask, two-layer filtered through gauze is gone out mycelia, collects filtrate and is the liquid culture metabolite through the bacteria-free filtrate of the miillpore filter preparation of 0.45 micron of diameter.Embodiment 8: the application of the liquid culture metabolite of mould penicillium striatisporum
Pot experiment with cucumber is an example: use the Tween-20 of 0.05-0.1% to dilute 200 times the liquid culture metabolite, the cucumber seedling of 2 true leaves is soaked root at dilution planted after 30 minutes, after planting, waters at root with 20-50 milliliter dilution again cucumber seedling, can prevent the mould Phytophthoradrechsleri Tucker of Jue Shi epidemic disease to infect the cucumber eqpidemic disease that causes, preventive effect reaches 30-60%.
Embodiment 9: the application of the liquid culture metabolite of mould penicillium striatisporum
Use with tomato plant and to be example: with the liquid culture metabolite with 150 times of the Tween-20 dilutions of 0.05-0.1%, dilution is sprayed on the tomato plant, can prevent to infect the tomato late blight that causes by phytophthora infestans Phytophthorainfestans de Bary, obviously reduce the scab number on leaf, stem and the fruit, the decayed fruit rate reduces 20-45%.
In addition, at potato, tomato, melonly wait other crops to grow seedlings or carry out identical experiment when transplanting, can find mould penicillium striatisporum solid fungicide or contain the bacterial manure of mould penicilliumstriatisporum solid fungicide and the liquid culture metabolite of this mould penicillium striatisporum to the Phytophthora capsici Phytophthora capsici Leonian in the Phytophthora disease fungus, phytophthora infestans Phytophthora infestans de Bary, soybean phytophthora Phytophthoramegasperma Drecgsler, Phytophthora nicotianae Phytophthora nicotianae Breda Hann, the mould Phytophthora drechsleri of Jue Shi epidemic disease Tucker, the Sclerotinia sclerotiorum Sclerotiniasclerotonium of Sclerotinia, the Rhizoctonia solani Kuhn Rhizoctonia solani Kuhn of Rhizoctonia, cereal rhizoctonia Rhizoctonia Van der Hoeven, the rotten mould Pythium aphanidermatum of the melon and fruit of pythium, germ eqpidemic diseases such as the mould Pythium ultimum of ultimate corruption, stalk break, damping off, banded sclerotial blight, damping off etc. all have the better prevention effect, can effectively prevent these soil-borne diseases and jeopardize crops.

Claims (10)

1, the application of a kind of mould in the plant soil-borne diseases control is characterized in that: with the form control plant soil-borne diseases of mould penicillium striatisporum with the liquid culture metabolite of solid fungicide form, solid fungicide and solid organic fertilizer compatibility form and this mould.
2. the application of a kind of mould according to claim 1 in the plant soil-borne diseases control, it is characterized in that: described mould penicillium striatisporum solid fungicide is to obtain like this: with the preservation bacterial classification of mould penicillium striatisporum insert carry out the test tube slant activation in the test tube slant medium after, inserting the capacity that liquid nutrient medium is housed again is the triangular flask of 250ml, and liquid amount is 80ml/250ml; Place shaking table to cultivate 3-4 days triangular flask, the rotating speed 160r/min of shaking table, the environmental temperature of culture period is 28 ± 2 ℃; Finish the back and in 28 ± 2 ℃ of environment, continue to cultivate 6-8 days, turned once every 2-3 days, to producing spore with 5% inoculum concentration (V/W) access solid culture medium; Pulverized the 10-20 mesh sieve after last natural air drying or 30 ℃ of oven dry, and obtained solid fungicide, the bacteria containing amount in the solid fungicide is 10 10-11Cfu/g.
3, the application of a kind of mould according to claim 2 in the plant soil-borne diseases control, it is characterized in that: described test tube slant medium is: glucose 10 grams, peptone 5 grams, KH 2PO 41 gram, MgSO47H 2O 0.5 gram, agar 15-20 gram, pH nature, 1000 milliliters in water; Described liquid nutrient medium is: glucose 10 grams, peptone 5 grams, KH 2PO 41 gram, MgSO47H 2The O0.5 gram, pH nature, 1000 milliliters in water; Described solid culture medium is: wheat bran, the peat composed of rotten mosses, vermiculite, their quality proportioning is 1: 3: 1.
4, the application of a kind of mould according to claim 1 in the plant soil-borne diseases control, it is characterized in that: described liquid culture metabolite is to obtain like this: with the preservation bacterial classification of mould penicilliumstriatisporum insert carry out the test tube slant activation in the test tube slant medium after, inserting the capacity that liquid fermentation medium is housed again is the triangular flask of 250ml, and liquid amount is 80ml/250ml; The rotating speed 160r/min of shaking table, the environmental temperature of culture period is 28 ± 2 ℃; Place the shaking table cultivation after 6-8 days triangular flask, two-layer filtered through gauze is removed mycelia, collects filtrate and is the liquid culture metabolite through the bacteria-free filtrate of the miillpore filter preparation of 0.45 micron of diameter.
The application of 5 a kind of moulds according to claim 1 in the plant soil-borne diseases control, it is characterized in that: described liquid fermentation medium is preparation like this: take by weighing potato 200 grams, peeling, be cut into piece and boil half an hour, use two-layer filtered through gauze then, add glucose 20 gram again, supply water to 1000 milliliter after dissolving, 121 ℃ of autoclavings 20 minutes obtain liquid fermentation medium.
6, the application of a kind of mould according to claim 1 in the plant soil-borne diseases control, it is characterized in that: described solid fungicide form control plant soil-borne diseases is to spread manuer in holes in crop root part after solid fungicide is mixed thoroughly with 5-8 times of vegetable garden soil, every cave contains solid fungicide 0.1-0.3 gram, or is 1 with solid fungicide with the native weight proportion of growing seedlings, and: 200-500 mixes and afterwards adorns alms bowl and grow seedlings; Solid fungicide and solid organic fertilizer compatibility form control plant soil-borne diseases are with solid fungicide and solid organic fertilizer compatibility, and weight proportion is 1: 50-100 spreads manuer in holes in the plant root after mixing, the 15-20 that whenever spreads manuer in holes gram; Described liquid culture metabolite form control plant soil-borne diseases is that the liquid culture metabolite is used for the root pouring or is sprayed on plant after doubly with the Tween-20 dilution 100-200 of 0.05%-0.1%, and every strain irrigation amount was a 20-50 milliliter dilution when wherein root watered.
7, the application of a kind of mould according to claim 6 in plant soil-borne diseases control is characterized in that: described solid organic fertilizer be agricultural solid residue through biofermentation, deodorization, dewater, through the fertilizer of the back formation of becoming thoroughly decomposed.
8, the application of a kind of mould according to claim 7 in the plant soil-borne diseases control, it is characterized in that: described agricultural solid residue comprises: various offcuts and waste that the deep development of feces of livestock and poultry, agricultural crop straw, primary agricultural products brings.
9, the application in the plant soil-borne diseases control according to claim 1 or 6 described a kind of moulds, it is characterized in that: described soil-borne disease refers to by soilborne Phytophthora, Sclerotinia, Rhizoctonia, pythium disease fungus.
10, the application of a kind of mould according to claim 9 in the plant soil-borne diseases control, it is characterized in that: described Phytophthora disease fungus comprises: Phytophthora capsici Phytophthora capsiciLeonian, phytophthora infestans Phytophthora infestans de Bary, soybean phytophthora Phytophthoramegasperma Drecgsler, Phytophthora nicotianae Phytophthora nicotianae Breda Hann, the mould Phytophthora drechsleri of Jue Shi epidemic disease Tucker; Described Sclerotinia disease fungus comprises: Sclerotinia sclerotiorum Sclerotinia sclerotonium; Described Rhizoctonia disease fungus comprises: Rhizoctonia solani Kuhn Rhizoctonia solani Kuhn, cereal rhizoctonia Rhizoctonia Van der Hoeven; Described pythium disease fungus comprises: the rotten mould Pythium aphanidermatum of melon and fruit, the mould Pythium ultimum of ultimate corruption.
CNB2005100389792A 2005-04-20 2005-04-20 Application of blue mould in preventing and treating plant soil infected disease Expired - Fee Related CN1270610C (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102887790A (en) * 2012-10-24 2013-01-23 山东金正大生态工程股份有限公司 Biological disease-prevention controlled-release ginger additional fertilizer, and preparation method and application thereof
CN103300083A (en) * 2013-05-15 2013-09-18 南京农业大学 Method for improving bread baking characteristic by using recombination lipoxygenase
CN113875478A (en) * 2021-10-25 2022-01-04 山东农业大学 Application of mixed fermentation product of penicillium commune and lactobacillus reuteri in reducing apple continuous cropping obstacle
CN115251087A (en) * 2022-08-08 2022-11-01 河南科技大学 Application of wheat root endophytic fungi G11 in prevention and treatment of wheat sharp eyespot

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102887790A (en) * 2012-10-24 2013-01-23 山东金正大生态工程股份有限公司 Biological disease-prevention controlled-release ginger additional fertilizer, and preparation method and application thereof
CN103300083A (en) * 2013-05-15 2013-09-18 南京农业大学 Method for improving bread baking characteristic by using recombination lipoxygenase
CN113875478A (en) * 2021-10-25 2022-01-04 山东农业大学 Application of mixed fermentation product of penicillium commune and lactobacillus reuteri in reducing apple continuous cropping obstacle
CN113875478B (en) * 2021-10-25 2022-09-06 山东农业大学 Application of mixed fermentation product of penicillium commune and lactobacillus reuteri in reducing apple continuous cropping obstacle
CN115251087A (en) * 2022-08-08 2022-11-01 河南科技大学 Application of wheat root endophytic fungi G11 in prevention and treatment of wheat sharp eyespot

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