CN113957010A

CN113957010A - Pseudomonas chlororaphis orange subspecies and preparation and application of microbial agent thereof

Info

Publication number: CN113957010A
Application number: CN202111305468.8A
Authority: CN
Inventors: 刘峰; 潘明; 王江伟; 陈小奇
Original assignee: Shandong Wfs Eco Engineering Co ltd
Current assignee: Shandong Wfs Eco Engineering Co ltd
Priority date: 2020-07-01
Filing date: 2020-07-01
Publication date: 2022-01-21
Anticipated expiration: 2040-07-01
Also published as: CN113957010B; CN113930363B; CN111705020A; CN113930363A; CN111705020B

Abstract

The invention discloses a Pseudomonas chlororaphis orange subspecies and preparation and application of a microbial agent thereof, the Pseudomonas chlororaphis orange subspecies 2501 disclosed by the invention has a sterilization function and an insecticidal function, and fills the gap that the existing Pseudomonas chlororaphis only has a single biocontrol function; also discloses a pseudomonas chlororaphis orange subspecies 2501 liquid microbial agent II, which comprises the following components: tween 80, trehalose, sucrose, orange peel essential oil and 2501 liquid microbial agent I; the solid microbial agent II of the pseudomonas chlororaphis orange subspecies 2501 comprises the following components in parts by weight: glucose, soybean meal powder, potassium fulvate and 2501 solid microbial agent I; and the obvious application effect is achieved through field experiments.

Description

Pseudomonas chlororaphis orange subspecies and preparation and application of microbial agent thereof

The application is divisional application with application number 202010627097.4, application date 20200701 and invention name 'preparation and application of Pseudomonas chlororaphis orange subspecies and microbial agent thereof'.

Technical Field

The invention belongs to the technical field of microorganisms, and particularly relates to a pseudomonas chlororaphis orange subspecies and preparation and application of a microbial agent thereof.

Background

At present, microbial agents for biological control of crop diseases and insect pests are various in types and have different use effects, most microbial agents for biological control have single effects of controlling the crop diseases and insect pests, only fungal diseases or single insect pests can be controlled, the types of the microbial agents for controlling the fungal diseases and the insect pests are few, and the types of the microbial agents for controlling various fungal diseases and various insect pests are few.

Fungal diseases and insect pests of crops often occur simultaneously, people also need to control the insect pests while controlling the fungal diseases, and if pure chemical pesticides are used for controlling, not only is environmental pollution easily caused, but also the crop products are damaged by pesticide residues; if the microbial agent and the chemical pesticide are used in a combined manner, the microbial agent and the chemical pesticide can not be mixed for use, so that the use effect of the microbial agent is easily reduced, and the microbial agent and the chemical pesticide need to be used separately; if the microbial agent is completely used for prevention and treatment, a plurality of microbial agents are required to be used, so that the economic cost is increased.

The research and development of multifunctional microbial agents for simultaneously preventing and treating various fungal diseases and various insect pests are problems which are urgently needed to be solved by the market at present.

Chinese patent document CN109258695A (application number: 201811214677.X) discloses the application of Pseudomonas chlororaphis in nematode control, the invention discloses the application of Pseudomonas chlororaphis with the preservation number GDMCC No.60273 in preparing biological microbial inoculum for nematode control, but does not relate to the action of preventing and controlling fungal diseases and other various pests.

Chinese patent document CN107099474A (application number: 201710333734.5) discloses Pseudomonas chlororaphis with broad-spectrum antibacterial activity and application thereof, and the invention discloses Pseudomonas chlororaphis CCTCC NO: m2016099 discloses that the bacterium has biological control effect on apple ring rot, cherry blight, grape anthracnose, grape downy mildew and wheat sharp eyespot, but does not relate to application of controlling crop pests.

The invention content is as follows:

aiming at the defects of the prior art, the invention provides a Pseudomonas chlororaphis orange subspecies and preparation and application of a microbial agent thereof.

The microbial agent prepared by the pseudomonas chlororaphis orange subspecies can effectively prevent and treat pathogenic fungi of various crops and can also effectively prevent and treat plant diseases and insect pests of various crops; the microbial inoculum related to the invention has the advantages of good germ-proof and insect-proof effects, strong broad spectrum and less use times, reduces the use amount of chemical pesticides, improves the quality of agricultural products, saves the cost, improves the economic benefit and protects the environment.

The technical scheme of the invention

Pseudomonas chlororaphis subsp. aurantiaca 2501, deposited in China general microbiological culture Collection center on 6.2.2020 with the deposition address: the No. 3 Xilu No.1 of Beijing, Chaoyang, the preservation number is CGMCC NO. 19900.

Pseudomonas chlororaphis orange subspecies 2501 morphological characteristics: on KMB medium, the colony is round and flat, wet, gram-negative, green pigment is produced in the early culture stage, and orange-yellow pigment is produced in the later culture stage.

The Pseudomonas chlororaphis orange subspecies 2501 is obtained by screening of Wufusheng ecological engineering Co., Ltd.

The preparation method of the pseudomonas chlororaphis orange subspecies 2501 fermentation product comprises the following steps:

(1) activating Pseudomonas chlororaphis orange subspecies 2501 on a solid culture medium, wherein the culture temperature is 30 +/-0.5 ℃, and the culture time is 48 hours, so as to prepare an activated strain;

(2) inoculating the activated strain in the step (1) into a primary liquid seed culture medium, wherein the culture temperature is 30 +/-0.5 ℃, the rotation speed is 180-;

(3) inoculating the primary seed liquid prepared in the step (2) into a secondary seed liquid culture medium, wherein the inoculation amount is 3-5 per thousand according to volume fraction, the culture temperature is 30 +/-0.5 ℃, the culture time is 12-15h, the rotation speed is 200 plus one-year-old 250rpm, and the ventilation amount is 1.0-1.2vvm, so as to prepare a secondary seed liquid;

(4) inoculating the secondary seed liquid prepared in the step (3) into a tertiary seed liquid culture medium, wherein the inoculation amount is 5-10% by volume fraction, the culture temperature is 30 +/-0.5 ℃, the culture time is 6-9h, the rotation speed is 150-200rpm, and the ventilation volume is 1.0-1.2vvm, so as to prepare the tertiary seed liquid;

(5) inoculating the three-level seed liquid prepared in the step (4) into a liquid fermentation culture medium, wherein the inoculation amount is 5-10% by volume fraction, the culture temperature is 30 +/-0.5 ℃, the culture time is 28-32h, the rotation speed is 100-150rpm, and the ventilation amount is 0.8-1.2vvm, so as to prepare a liquid fermentation product, namely the green needle pseudomonas orange subspecies 2501 liquid microbial agent I;

(6) and (3) drying the fermentation liquor prepared in the step (5) to prepare a solid fermentation product, namely the pseudomonas chlororaphis orange subspecies 2501 solid microbial agent I.

Preferably, the composition of the solid medium of step (1) according to the present invention is as follows: 10g/L of tryptone, 5g/L of yeast powder, 10g/L of sodium chloride, 5g/L of glucose, 18-20g/L of agar and the balance of water, wherein the pH value is 7.0-7.2.

Preferably, the composition of the primary liquid seed culture medium in step (2) is as follows: 10g/L of tryptone, 5g/L of yeast powder, 10g/L of sodium chloride, 5g/L of glucose and the balance of water, wherein the pH value is 7.0-7.2.

Preferably, according to the present invention, the rotation speed in step (2) is 190-.

Preferably, according to the present invention, the composition of the secondary seed liquid medium in step (3) is as follows: 10g/L of tryptone, 5g/L of yeast powder, 10g/L of sodium chloride, 5g/L of glucose and the balance of water, wherein the pH value is 7.0-7.2.

According to the invention, the inoculation amount in the step (3) is 3.5-5 per mill by volume fraction, the culture temperature is 30 +/-0.5 ℃, the culture time is 14-15h, the rotating speed is 220-250rpm, and the ventilation volume is 1.1-1.2 vvm.

Preferably, the composition of the tertiary seed liquid culture medium in the step (4) is as follows by mass fraction: pancreatic bean pulp 0.2%, corn flour 1%, glucose 1%, peptone 0.5%, magnesium sulfate 0.1%, ammonium sulfate 0.1%, potassium dihydrogen phosphate 0.05%, dipotassium hydrogen phosphate 0.05%, and water in balance, wherein the pH value is 7.2-7.5.

According to the invention, the inoculum size in step (4) is preferably 6-10% by volume fraction, the cultivation temperature is 30. + -. 0.5 ℃, the cultivation time is 7-9h, the rotation speed is 160-.

According to the invention, the volume fraction of the inoculum in step (5) is preferably 6-10%, the cultivation temperature is 30. + -. 0.5 ℃, the cultivation time is 29-32h, the rotation speed is 130-.

Preferably, the liquid fermentation medium in step (5) has the following composition according to the present invention: 1% of soybean meal, 3% of corn flour, 1% of glucose, 0.5% of peptone, 0.2% of magnesium sulfate, 0.3% of ammonium sulfate, 0.1% of monopotassium phosphate, 0.1% of dipotassium phosphate and the balance of water, wherein the pH value is 7.2-7.5.

Preferably, the effective viable count of the fermentation liquid prepared in the step (5) is 3.5 multiplied by 10¹⁰cfu/mL or more.

According to the present invention, the effective viable count of the solid microbial agent in the step (6) is preferably 2X 10¹¹cfu/g or more.

Preferably, according to the invention, the drying process in step (6) is a spray drying process.

Application of Pseudomonas chlororaphis orange subspecies 2501 and/or Pseudomonas chlororaphis orange subspecies 2501 leavening in biological control of crops.

According to the invention, the Pseudomonas chlororaphis subsp.aurantium 2501 and/or the Pseudomonas chlororaphis subsp.aurantium 2501 ferment is preferably used for preventing and treating fungal diseases and insect pests of crops.

According to the invention, the fermentation product of the pseudomonas chlororaphis subspecies aurantiacus 2501 and/or the pseudomonas chlororaphis subspecies aurantiacus 2501 is diluted by water until the effective viable count is 1 x 10 when the fungal diseases and insect pests of crops are controlled⁸cfu/(mL/g) or more.

The pseudomonas chlororaphis orange subspecies 2501 liquid microbial agent II comprises the following components in parts by weight: 0.03-0.08 part of Tween 80, 0.03-0.08 part of trehalose, 1-3 parts of sucrose, 0.005-0.015 part of orange peel essential oil and 96.83-98.94 parts of Pseudomonas chlororaphis orange subspecies 2501 liquid microbial agent I.

According to the invention, the preferable liquid microbial agent II of the pseudomonas chlororaphis orange subspecies 2501 comprises the following components in parts by weight: 0.05 part of Tween 80, 0.05 part of trehalose, 2 parts of sucrose, 0.008 part of orange peel essential oil and 97.89 parts of Pseudomonas chlororaphis orange subspecies 2501 liquid microbial agent I.

The preparation method of the pseudomonas chlororaphis orange subspecies 2501 liquid microbial agent II comprises the following steps:

uniformly mixing 0.03-0.08 part by weight of Tween 80, 0.03-0.08 part by weight of trehalose, 1-3 parts by weight of sucrose, 0.005-0.015 part by weight of orange peel essential oil and 96.83-98.94 parts by weight of the prepared Pseudomonas chlororaphis orange subspecies 2501 liquid microbial agent I to obtain the Pseudomonas chlororaphis orange subspecies 2501 liquid microbial agent II.

According to the invention, the preferred preparation method of the pseudomonas chlororaphis orange subspecies 2501 liquid microbial agent II comprises the following steps:

uniformly mixing 0.05 part by weight of Tween 80, 0.05 part by weight of trehalose, 2 parts by weight of sucrose, 0.008 part by weight of orange peel essential oil and 97.89 parts by weight of Pseudomonas chlororaphis orange subspecies 2501 liquid microbial agent I to obtain Pseudomonas chlororaphis orange subspecies 2501 liquid microbial agent II.

Application of pseudomonas chlororaphis orange subspecies 2501 liquid microbial agent II in biological control of crops.

According to the invention, the optimized application of the pseudomonas chlororaphis orange subspecies 2501 liquid microbial agent II in the control of fungal diseases and insect pests of crops.

The solid microbial agent II of the pseudomonas chlororaphis orange subspecies 2501 comprises the following components in parts by weight: 20-30 parts of glucose, 15-25 parts of soybean meal, 25-35 parts of potassium fulvate and 10-30 parts of the pseudomonas chlororaphis orange subspecies 2501 solid microbial agent I.

According to the invention, the preferable solid microbial agent II of the pseudomonas chlororaphis orange subspecies 2501 comprises the following components in parts by weight: 30 parts of glucose, 20 parts of soybean meal, 30 parts of potassium fulvate and 20 parts of pseudomonas chlororaphis orange subspecies 2501 solid microbial agent I.

The preparation method of the solid microbial agent II of the pseudomonas chlororaphis orange subspecies 2501 comprises the following steps:

uniformly mixing 20-30 parts by weight of glucose, 15-25 parts by weight of soybean meal, 25-35 parts by weight of potassium fulvate and 10-30 parts by weight of the solid microbial agent I of the orange subspecies 2501 of the pseudomonas chlororaphis to prepare the solid microbial agent II of the orange subspecies 2501 of the pseudomonas chlororaphis.

According to a preferred embodiment of the present invention, the method for preparing solid microbial inoculant II of Pseudomonas chlororaphis subsp.aurantium 2501 comprises the following steps:

the components in parts by weight are as follows: 30 parts of glucose, 20 parts of soybean meal, 30 parts of potassium fulvate and 20 parts of solid microbial agent I of the pseudomonas chlororaphis orange subspecies 2501 are uniformly mixed to prepare the solid microbial agent II of the pseudomonas chlororaphis orange subspecies 2501.

Application of solid microbial agent II of Pseudomonas chlororaphis orange subspecies 2501 in biological control of crops.

According to the invention, the application of the pseudomonas chlororaphis orange subspecies 2501 solid microbial agent II in the control of fungal diseases and insect pests of crops is preferable.

The technical scheme of the invention has the beneficial effects

1. High broad spectrum property

The pseudomonas chlororaphis subspecies orange 2501 related by the invention has control effects on crop pests such as apple cabbage looper, wheat pipe thrips, scarab beetle, ladybug, colorado potato beetle, weevil, stinkbug and the like besides control effects on root rot and sclerotinia caused by fusarium and sclerotinia sclerotiorum.

2. Good insecticidal effect

The control effect of the pseudomonas chlororaphis orange subspecies 2501 related by the invention on pests can reach more than 80%.

3. Safe and environment-friendly

The pseudomonas chlororaphis orange subspecies 2501 related by the invention is obtained by screening and separating from the protected field of the cultivated land of the shou vegetables in Shandong, is not subjected to gene modification, has no risk when used in the field, and the secreted sterilization and insecticidal substances are small molecular cyclic peptides and lipopeptides, can be naturally and rapidly decomposed in soil, are safe to crops, animals and human bodies, can realize no pollution and no residue in the field, the crops and water sources, greatly improves the safety compared with the conventional sterilization and insecticide, and is beneficial to the development of organic agriculture.

Detailed Description

The invention is further illustrated with reference to the following specific examples, without limiting the scope of the invention thereto.

The contents of the examples, which are not specified in specific conditions, were carried out under conventional conditions; the reagents or instruments used are not indicated by the manufacturer, and are all common commercial products.

Pseudomonas chlororaphis subsp. aurantiaca 2501 is hereinafter abbreviated as 2501;

pseudomonas aeruginosa BNCC 190697: purchased from the institute of biotechnology, Chuanglian, Beijing;

fusarium oxysporum, Botrytis cinerea, Helminthosporium gramineum, trichotheca roseum: provided by Shandong provincial academy of sciences, the same kind of bacteria can be purchased for replacement in the existing strain preservation center;

phytophthora: the strain is separated from Wang ditch town strawberry field in Linyi orchid mountain area, and can be replaced by the same strain purchased from the existing strain preservation center;

sclerotinia sclerotiorum and verticillium dahliae: provided by Xinjiang Nongkouchi, the same kind of bacteria can be purchased for replacement in the existing strain preservation center;

pseudomonas solanacearum BNCC 335855: purchased from the institute of biotechnology, Chuanglian, Beijing.

Examples 1 to 1

The screening of Pseudomonas chlororaphis subspecies orange 2501 comprises the following steps:

separation of bacteria in the longevity vegetable protected area: the KMB, LB culture medium and nutrient agar culture medium are used for separating bacteria in soil and roots and stems of healthy plants, and 126 bacterial strains are separated.

1. Further screening the separated and purified bacteria by using plant pathogenic fungi as targets

Transferring test plant pathogenic fungi (Fusarium oxysporum, Phytophthora, Sclerotinia sclerotiorum) stored in a refrigerator at 4 deg.C to a PDA plate for activation, culturing at 30 deg.C for 3d, separating and purifying bacteria from the protective land of the vegetable by plate confronting method, and determining antibacterial activity of the test plant pathogenic fungi as target. The specific method comprises the following steps: after pathogenic bacteria grow on the flat plate, punching a fungus cake (phi 5mm) by using a puncher, inversely pasting the fungus cake in the center of a PDA flat plate, selecting separated bacteria (cultured on an LB solid culture medium at 30 ℃ for 2d) and inoculating the bacteria to three corners equidistant from the pathogenic bacteria in parallel, wherein the distance from the inoculated separated bacteria to the center of the pathogen fungus cake is 30mm, the bacteria are cultured at 30 ℃ for 3d, observing whether antagonism exists or not, and measuring the width of a bacteriostasis belt, wherein the width of the bacteriostasis belt refers to the width of a transparent belt on a connecting line connecting the inoculation point of the separated bacteria and the center point of the pathogen fungus cake; the width of the zone of inhibition is used as the mark of the strength of antagonism, and the detection results of the zone of inhibition of different bacterial strains to plant pathogenic bacteria are shown in table 1.

TABLE 1

Note: the strains listed in the table are strains with relatively good bacteriostatic effect.

As can be seen from Table 1, the bacterial strain 2501 showed a high bacteriostatic effect against the three phytopathogens.

2. Further screening the separated and purified bacteria by using apple noctuid and wheat tubthrips as targets

Respectively inoculating the separated different bacteria with parallel LB liquid culture medium according to the same inoculation amount, culturing at 30 ℃ for 2d to obtain different bacteria fermentation liquor, diluting the obtained fermentation liquor by 50 times, then respectively soaking the cut apple round leaves in the different bacteria fermentation liquor for 10s, taking out and naturally drying, placing in a culture dish, respectively inoculating 30 heads of apple night moths with the same size, sealing with a sealing film and puncturing holes to ensure normal breathing of the test insects. And (4) observing survival conditions of the treated test insects after 24h, and calculating the death rate by using a brush to lightly touch the test insects without response as dead insects. Each treatment was repeated 3 times with sterile water treatment as a blank CK.

And (3) respectively taking 1ml to 5ml of the diluted different bacteria fermentation liquid by 50 times, covering a tube cover, uniformly shaking and rolling for several minutes, pouring out the bacteria liquid when the bacteria liquid is uniformly distributed in the tube, naturally airing indoors, and preparing into a bacterial film. The selected 30 wheat pipe thrips are placed in a pipe (a pipe cover is punctured), crawled for 1h, transferred into another 10ml clean pipe, fresh wheat leaves are placed in the clean pipe for feeding, and the cotton ball is sealed. The treated test insects are put into an artificial climate box for culturing, the survival conditions of the test insects in each treatment are respectively observed after 72 hours, the test insects are lightly touched by a brush pen brush and do not react to form dead insects, the death rate is calculated, each treatment is repeated for 3 times, a blank control group CK is treated by sterile water, and the effect results of the treatment on the test insects of the apple looper and the test insects of the wheat pipelining thrips are shown in a table 2.

TABLE 2

Note: the strains listed in the table are strains with relatively good insecticidal effect.

It can be seen from table 2 that the strain number 2501 is the highest in lethality against both pests.

Examples 1 to 2

Morphological characteristics of the 2501 strain: gram staining was negative, colonies were round, flat, wet on KMB solid medium, producing green pigment during the initial stage of culture and orange pigment during the later stage of culture, and was designated as Pseudomonas chlororaphis subsp.

Morphological characteristics of 1018 strain: on KMB medium, the colonies were round, flat, wet, gram-negative, producing green pigment in the initial stage of culture and orange-yellow pigment in the later stage of culture, and were small compared with 2501 for the same period of culture, and they were named as Pseudomonas chlororaphis (Pseudomonas chlororaphis) and named as Pseudomonas chlororaphis 1018.

The Pseudomonas chlororaphis subsp. aurantiaca 2501 is deposited in the China general microbiological culture Collection center on 6.2.2020, Beijing, Kyowa, Asahi-Chen-Xilu No.1, the institute of microbiology, China academy of sciences, and the deposition number is CGMCC NO. 19900.

Example 2-1

A process for the preparation of 2501 fermentates comprising the steps of:

(1) activating strains: activating pseudomonas aeruginosa orange subspecies 2501 on a solid culture medium, wherein the culture temperature is 30 +/-0.5 ℃, and the culture time is 48 h;

the composition of the solid medium was as follows: 10g/L of tryptone, 5g/L of yeast powder, 10g/L of sodium chloride, 5g/L of glucose, 17g/L of agar and the balance of water, wherein the pH value is 7.2-7.4.

(2) Preparing a first-level seed solution: inoculating the activated strain in the step (1) into a primary liquid seed culture medium, wherein the culture temperature is 30 +/-0.5 ℃, the rotation speed is 190-;

the first-stage liquid seed culture medium comprises the following components: 10g/L of tryptone, 5g/L of yeast powder, 10g/L of sodium chloride, 5g/L of glucose and the balance of water, wherein the pH value is 7.2-7.4.

(3) Preparing a secondary seed solution: inoculating the primary seed liquid prepared in the step (2) into a secondary seed liquid culture medium, wherein the inoculation amount is 3.5-5 per mill according to volume fraction, the culture temperature is 30 +/-0.5 ℃, the culture time is 14-15h, the rotation speed is 220 plus-one 250rpm, and the ventilation amount is 1.1-1.2vvm, so as to prepare the secondary seed liquid.

The components of the secondary seed liquid culture medium are as follows: 10g/L of tryptone, 5g/L of yeast powder, 10g/L of sodium chloride, 5g/L of glucose and the balance of water, wherein the pH value is 7.2-7.4.

(4) Preparing a third-level seed solution: inoculating the secondary seed liquid prepared in the step (3) into a tertiary seed liquid culture medium, wherein the inoculation amount is 6-10% by volume fraction, the culture temperature is 30 +/-0.5 ℃, the culture time is 7-9h, the rotation speed is 160-200rpm, and the ventilation volume is 1.1-1.2vvm, so as to prepare the tertiary seed liquid.

The components of the third-level seed liquid culture medium are as follows: 0.2% of soybean meal, 1% of corn flour, 1% of glucose, 0.5% of peptone, 0.1% of magnesium sulfate, 0.1% of ammonium sulfate, 0.05% of monopotassium phosphate, 0.05% of dipotassium phosphate and the balance of water, wherein the pH value is 7.2-7.4.

(5) Preparing fermentation liquor: inoculating the three-stage seed liquid prepared in the step (4) into a liquid fermentation culture medium, wherein the inoculation amount is 6-10% by volume fraction, the culture temperature is 30 +/-0.5 ℃, the culture time is 29-32h, the rotating speed is 130-150rpm, and the ventilation volume is 1.0-1.2vvm, so as to prepare a liquid fermentation product, namely 2501 liquid microbial agent I, and the effective viable count is 3.5 multiplied by 10¹⁰cfu/mL。

The components of the liquid fermentation culture are as follows: 1% of soybean meal, 3% of corn flour, 1% of glucose, 0.5% of peptone, 0.2% of magnesium sulfate, 0.3% of ammonium sulfate, 0.1% of monopotassium phosphate, 0.1% of dipotassium phosphate and the balance of water, wherein the pH value is 7.2-7.4.

(6) Spray drying the fermentation liquor prepared in the step (5) to prepare a solid fermentation product, namely 2501 solid microbial agent I with the effective viable count of 2 multiplied by 10¹¹cfu/g。

Examples 2 to 2

A process for the preparation of 2501 fermentates comprising the steps of:

(2) Preparing a first-level seed solution: inoculating the activated strain in the step (1) into a primary liquid seed culture medium, wherein the culture temperature is 30 +/-0.5 ℃, the rotation speed is 180-;

(3) Preparing a secondary seed solution: inoculating the primary seed liquid prepared in the step (2) into a secondary seed liquid culture medium, wherein the inoculation amount is 3-5 per mill, the culture temperature is 30 +/-0.5 ℃, the culture time is 12-15h, the rotation speed is 200 plus-minus-one 250rpm, and the ventilation volume is 1.0-1.2vvm, so as to prepare the secondary seed liquid.

(4) Preparing a third-level seed solution: inoculating the secondary seed liquid prepared in the step (3) into a tertiary seed liquid culture medium, wherein the inoculation amount is 5-10%, the culture temperature is 30 +/-0.5 ℃, the culture time is 6-9h, the rotation speed is 150-plus-one 200rpm, and the ventilation volume is 1.0-1.2vvm, so as to prepare the tertiary seed liquid.

The components of the third-level seed liquid culture medium are as follows: pancreatic bean pulp 0.2%, corn flour 1%, glucose 1%, peptone 0.5%, magnesium sulfate 0.1%, ammonium sulfate 0.1%, potassium dihydrogen phosphate 0.05%, dipotassium hydrogen phosphate 0.05%, and water in balance, wherein the pH value is 7.2-7.4.

(5) Preparing fermentation liquor: inoculating the third-stage seed liquid prepared in the step (4) into liquid fermentation culture

The inoculation amount of the medium is 5-10%, the culture temperature is 30 +/-0.5 ℃, and the culture time is 28-32hThe rotation speed is 100-150rpm, the ventilation amount is 0.8-1.2vvm, the liquid fermentation product, namely 2501 liquid microbial agent I is prepared, the effective viable count is 2.0 multiplied by 10¹⁰cfu/mL。

The components of the liquid fermentation culture are as follows: 0.5% of soybean meal, 3% of corn flour, 0.5% of glucose, 0.5% of peptone, 0.2% of magnesium sulfate, 0.5% of ammonium sulfate, 0.1% of monopotassium phosphate, 0.1% of dipotassium phosphate and the balance of water, wherein the pH value is 7.2-7.4.

(6) Spray drying the fermentation liquor prepared in the step (5) to prepare a solid fermentation product, namely 2501 solid microbial agent I with the effective viable count of 1.25 multiplied by 10¹¹cfu/g。

Comparative example 2-1

The difference from example 2-1 is that 1018 strains were fermented and cultured to obtain 1018 liquid microbial preparation I having the same viable cell count as that of 2501 liquid microbial preparation I and to obtain 1018 solid microbial preparation I having the same viable cell count as that of 2501 solid microbial preparation I.

Comparative examples 2 to 2

The difference from example 2-1 is that Pseudomonas chlororaphis BNCC190697 was subjected to fermentation culture to obtain BNCC190697 liquid microbial agent I having the same viable count as 2501 liquid microbial agent I and obtain BNCC190697 solid microbial agent I having the same viable count as 2501 solid microbial agent I.

Effect example 2-1

Antagonistic experiment of different strains of Pseudomonas chlororaphis on partial plant pathogenic bacteria

Respectively taking 100 μ L of 10⁸The surface of a PDA solid culture medium plate is coated with cfu/mL of different plant pathogen dilution liquid, then 1 sterile Oxford cup (6mm multiplied by 7.8mm multiplied by 10mm) is placed in the center of each plate, the Oxford cup is lightly pressed to make the Oxford cup contact with the culture medium without a gap, 300 mu L of Pseudomonas chlororaphis fermentation liquid produced by different methods is added into each Oxford cup, then the plate is placed in a 30 ℃ incubator for constant temperature culture, after 72 hours of culture, the diameter of a bacteriostatic ring of each sample is measured, the diameter of the bacteriostatic ring is the width of the bacteriostatic ring outside the Oxford cup, and the result is shown in Table 3.

TABLE 3

From table 3, it can be seen that the fermentation products of pseudomonas aeruginosa treated differently have bacteriostatic effects on pathogenic fungi and have no effect on pathogenic bacteria, but the bacteria have obvious differences in bacteriostatic effects on different pathogenic fungi, and the differences are not significant in the inhibition of fusarium oxysporum and verticillium dahliae, but are significant in the inhibition of phytophthora, botrytis cinerea, sclerotinia sclerotiorum, trichotheca roseum and helminthosporium graminearum, wherein the bacteriostatic effect of the example 2-1 is the best.

Effect examples 2-2

Insecticidal activity experiment of pseudomonas chlororaphis of different strains on spodoptera littoralis and thrips tritici

The pre-cut apple round leaves are respectively soaked in the pseudomonas chlororaphis fermentation liquor of different strains with the same viable count prepared by the same fermentation method for 10s, the green needle pseudomonas chlororaphis is taken out and naturally dried, the green needle pseudomonas chlororaphis is placed in a culture dish, 30 heads of apple cabbage loopers with the same size are respectively inoculated, the holes are punctured after the sealing membrane is used for sealing, and the normal breathing of the test insects is ensured. And (4) observing survival conditions of the treated test insects after 24h, and calculating the death rate by using a brush to lightly touch the test insects without response as dead insects. Each treatment was repeated 3 times with sterile water treatment as a blank CK.

Respectively taking 1ml to 5ml of pseudomonas chlororaphis fermentation liquor which is uniformly dispersed and produced by different methods, covering a pipe cover, uniformly shaking and rolling for a plurality of minutes, pouring out the bacteria liquid when the bacteria liquid is uniformly distributed in the pipe, naturally airing the bacteria liquid indoors, and preparing a bacteria film. The selected 30 wheat pipe thrips are placed in a pipe (a pipe cover is punctured), crawled for 1h, transferred into another 10ml clean pipe, fresh wheat leaves are placed in the clean pipe for feeding, and the cotton ball is sealed. And (3) culturing the treated test insects in an artificial climate box, observing survival conditions of the treated test insects after 72 hours, calculating mortality by using a brush to touch lightly and taking no response as dead insects, repeating each treatment for 3 times, and treating the blank control group CK with sterile water.

The results of the data analysis of the insecticidal test using the SPSS method are shown in table 4:

TABLE 4

Note: a has no significant difference, and b and c have significant difference

As can be seen from Table 4, 2501 had insecticidal effect against Spodoptera frugiperda and thrips tritici, and the control had no difference from BNCC190697 and had no insecticidal activity against Spodoptera frugiperda and thrips tritici.

Example 3-1

2501 liquid microbial agent II comprises the following components in parts by weight:

0.05 part of Tween 80, 0.05 part of trehalose, 2 parts of sucrose, 0.008 part of orange peel essential oil and 97.892 parts of 2501 liquid microbial agent I prepared in example 2-1;

the preparation method of the 2501 liquid microbial agent II comprises the following steps:

the 2501 liquid microbial agent II is obtained by uniformly mixing the components in corresponding parts by weight.

Examples 3 to 2

0.03 part of Tween 80, 0.05 part of trehalose, 3 parts of sucrose, 0.008 part of orange peel essential oil and 96.912 parts of 2501 liquid microbial agent I prepared in example 2-1;

Examples 3 to 3

0.05 part of Tween 80, 0.08 part of trehalose, 2 parts of sucrose, 0.015 part of orange peel essential oil and 97.855 parts of 2501 liquid microbial agent I prepared in example 2-1;

Examples 3 to 4

The difference from example 3-1 is that 2501 liquid microbial preparation I prepared in example 2-1 is changed to 2501 liquid microbial preparation I prepared in example 2-2 in the composition of 2501 liquid microbial preparation II.

Comparative example 3-1

The difference from example 3-1 is that 1018 liquid microbial preparation II was prepared by changing 2501 liquid microbial preparation I prepared in example 2-1 to 1018 liquid microbial preparation I prepared in comparative example 2-1 in the composition of the liquid microbial preparation II.

Comparative examples 3 to 2

The difference from example 3-1 is that trehalose is not added to the composition of 2501 liquid microbial preparation II, and sucrose is used in place of trehalose in parts by weight.

Comparative examples 3 to 3

The difference from example 3-1 is that 2501 liquid microorganism bacterium agent II contains no sucrose, and trehalose is used in place of sucrose in part by weight.

Comparative examples 3 to 4

Compared with the above example 3-1, the difference is that the 2501 liquid microbial agent II has no Tween 80, and glycerol is used to replace Tween 80 by weight.

Comparative examples 3 to 5

Compared with the above example 3-1, the difference is that 2501 liquid microbial agent II does not contain orange peel essential oil, and lemon essential oil is used to replace the weight part of the orange peel essential oil.

Comparative examples 3 to 6

The difference from example 3-1 above is that the composition of the liquid microbial inoculum II was changed from 2501 liquid microbial inoculum I prepared in example 2-1 to BNCC190697 liquid microbial inoculum I prepared in comparative example 2-2 to BNCC190697 liquid microbial inoculum II.

Effect example 3-1

And (3) respectively soaking pre-cut apple round leaves in 100 times of diluent of the liquid microbial agent II prepared in the examples 3-1, 3-2, 3-3 and 3-4 and the comparative examples 3-1, 3-2, 3-3, 3-4, 3-5 and 3-6 for 10s, taking out, naturally airing, placing in a culture dish, respectively inoculating apple epididymis with the same size, sealing with a sealing film, and puncturing to ensure normal breathing of the test insects. And (4) observing survival conditions of the treated test insects after 72h, and calculating the death rate by using a brush to lightly touch the test insects without response as dead insects. Each treatment was repeated 3 times, with sterile water treatment as a blank CK and the results of the treatments are tabulated in Table 5.

TABLE 5

Note: 1. percent reduction rate (%) is (number of live insects before application-number of live insects after application)/number of live insects before application x 100

2. Control effect (%) - (reduction rate of population in medicament treatment area-reduction rate of population in blank control area)/(reduction rate of population in 100-blank control area) x 100

3. The microbial inoculum is diluted by 100 times for use

a, the difference is not significant; b. c, d and e are obviously different

As can be seen from the data in Table 5, the fungicide prepared in example 3-1 has the best lethal effect on Spodoptera frugiperda, and the control effect can reach 90.74%; the experimental data show that the tween 80, the trehalose, the sucrose, the orange peel essential oil and the 2501 liquid microbial agent I are mixed to generate a certain synergistic effect, and the control effect on the apple leaf roller is obvious.

Effect examples 3 and 2

Respectively taking liquid microbial agents II1ml prepared in the embodiments 3-1, 3-2, 3-3 and 3-4 and the comparative examples 3-1, 3-2, 3-3, 3-4, 3-5 and 3-6 to 5ml of centrifugal tubes, covering tube covers, shaking uniformly and rolling for a plurality of minutes, pouring out bacterial liquid when the bacterial liquid is uniformly distributed in the tubes, naturally airing in a room to prepare bacterial films, wherein the concentration of the bacterial films is the concentration of the bacterial liquid. The selected 30 wheat pipe thrips are placed in a pipe (a pipe cover is punctured), crawled for 1h, transferred into another 10mL clean pipe, fresh wheat leaves are placed in the clean pipe for feeding, and the cotton ball is sealed. And (3) culturing the treated test insects in an artificial climate box, observing survival conditions of the treated test insects after 72 hours, calculating mortality by using a brush to touch lightly and taking no response as dead insects, repeating each treatment for 3 times, treating a blank control group CK with sterile water, and obtaining treatment results shown in table 6.

TABLE 6

a, the difference is not significant; b. c and d are obviously different

As can be seen from the data in Table 6, the microbial agent prepared in example 3-1 has the best lethal effect on the thrips tritici, and the control effect can reach 82.33%.

Effect examples 3 to 3

And (2) spraying the botrytis cinerea spore suspension on treated potted tomato plants by using a small sprayer, after the plants are diseased, respectively taking the liquid microbial agent II prepared in the examples 3-1, 3-2, 3-3 and 3-4 and the comparative examples 3-1, 3-2, 3-3, 3-4, 3-5 and 3-6, diluting by 50 times, spraying the diluted liquid onto each treated potted tomato plant by using the sprayer, wherein the spraying amount of each pot is 20mL, treating a blank control group CK by using sterile water, investigating the disease condition of each treatment group at the 3d and the 7d after treatment, counting the disease condition of each treatment, calculating the disease index and the control effect, and showing in a table 7.

TABLE 7

Note: the disease index ∑ (number of disease leaves at each stage × number of disease stages)/(number of survey leaves × number of highest disease stages) × 100; the preventing and treating effect (%) is (contrast disease index-treatment disease index)/contrast disease index is multiplied by 100

a has no significant difference, and b, c and d have significant difference

From table 7, it can be seen that the microbial agent prepared in example 3-1 has the best control effect on tomato gray mold, and the control effect can reach 79.53%, and from the above experimental data, it can be seen that the mixed use of tween 80, trehalose, sucrose, orange peel essential oil and 2501 liquid microbial agent I produces a certain synergistic effect, and the control effect on tomato gray mold is significant.

Example 4-1

2501 solid microbial agent II comprises the following components in parts by weight: 30 parts of glucose, 20 parts of soybean meal and 30 parts of potassium fulvate, wherein 20 parts of 2501 solid microbial agent I prepared in example 2-1;

the preparation method of the solid microbial agent comprises the following steps: the method comprises the following steps:

the 2501 solid microbial agent II is obtained by uniformly mixing the components in corresponding weight parts.

Example 4 to 2

2501 solid microbial agent II comprises the following components in parts by weight: 20 parts of glucose, 25 parts of soybean meal and 35 parts of potassium fulvate, wherein 20 parts of 2501 solid microbial agent I prepared in example 2-1;

Examples 4 to 3

2501 solid microbial agent II comprises the following components in parts by weight: 30 parts of glucose, 25 parts of soybean meal and 25 parts of potassium fulvate, wherein 20 parts of 2501 solid microbial agent I prepared in example 2-1;

Examples 4 to 4

The difference from example 4-1 is that 2501 solid microbial preparation I prepared in example 2-1 is changed to 2501 solid microbial preparation I prepared in example 2-2 in the composition of solid microbial preparation II.

Comparative example 4-1

The difference from example 4-1 is that 2501 solid microbial preparation I prepared in example 2-1 is replaced with 1018 solid microbial preparation I prepared in comparative example 2-1 in the composition of solid microbial preparation II.

Comparative examples 4 to 2

The difference from example 4-1 is that the solid microbial preparation II has a composition in which glucose is not added, and sucrose is used in place of glucose in parts by weight.

Comparative examples 4 to 3

Compared with the above example 4-1, the difference is that the solid microbial agent II has no soybean meal added, and peanut meal is used to replace the weight part of the soybean meal.

Comparative examples 4 to 4

Compared with the above example 4-1, the difference is that potassium fulvate is not added in the composition of the solid microbial agent II, and potassium humate is used to replace the weight part of potassium fulvate.

Comparative examples 4 to 5

Compared with the above example 4-1, the difference is that the 2501 solid microbial agent I prepared in the example 2-1 is changed into the BNCC190697 solid microbial agent I prepared in the comparative example 2-2 in the composition of the solid microbial agent II.

Effect example 4-1

Pot experiment: the method comprises the steps of taking wheat field ploughing layer soil, removing impurities such as stones and the like, then sieving the soil by a sieve with the aperture of 1.0cm, adding 15g/kg of organic fertilizer, 0.25g/kg of urea and 0.5g/kg of phosphate fertilizer, fully and uniformly mixing the soil and the organic fertilizer, and filling the mixture into plastic pots (the diameter is 14.5cm, the height is 11.5cm), wherein 1.5kg of soil is filled in each pot. Healthy cucumber seedlings (four leaves) with the same size are selected for transplanting, and 1 plant is planted in each pot. And managing according to conventional water and fertilizer measures.

Inoculation: spores of Fusarium oxysporum, which had a diameter of 90cm and were cultured on a PDA plate at 25 ℃ for 10 days, were scraped off and mixed uniformly into a spore suspension, which was divided into 10 portions of 100mL portions in parallel, and 20g of each of the solid microbial agents II prepared in examples 4-1, 4-2, 4-3, 4-4, comparative examples 4-1, 4-2, 4-3, 4-4, and 4-5 was mixed uniformly with 1 portion of the spore suspension to prepare a mixed solution, and sterile water was mixed uniformly with the spore suspension to prepare a control CK. And after the cucumber seedlings are transplanted for 5 days, inoculating the mixed solution and the reference solution CK by adopting a perfusion method, wherein each treatment corresponds to 3 pots of cucumber seedlings, and 100mL of the mixed solution is inoculated in each pot. And (4) carrying out normal management in the later period, digging out plants after 1 month of inoculation, counting the disease degree, calculating the disease index, and obtaining the control effect, wherein the treatment result is shown in a table 8.

TABLE 8

Note: 1. incidence rate (number of diseased plants/total number of plants) × 100%; 2. the disease index ∑ (number of each disease-level strain × representative level value)/(total number of strains × representative level value at the highest level of morbidity) × 100; 3. the prevention and treatment effect is [ control disease index-treatment disease index)/control disease index ] x 100%; 4. disease grading standard: grade 0, healthy root; grade I, the lower lateral roots of 1/5 are rotten; grade II, 1/5-1/3 lateral root rot; grade III, 1/3 to 2/3 lateral root rot; grade IV, the rotting of the lateral roots above 2/3 and even the death of the whole plant are 4, the difference is not obvious when the same letters are expressed, and the difference is obvious when different letters are expressed

As can be seen from table 8, in the laboratory cucumber potting experiment, the control effect of example 4-1 on cucumber root rot is the best, and the combination of glucose, bean pulp, potassium fulvate and 2501 solid microbial agent I produces a certain synergistic effect, so that the control effect on cucumber root rot is significant.

Effect example 4-2

Pot experiment: the method comprises the steps of taking plowing layer soil of the wheat field, removing impurities such as stones and the like, screening by a 1.0cm sieve, adding 25g/kg of organic fertilizer, 0.20g/kg of urea and 0.45g/kg of phosphate fertilizer, fully and uniformly mixing, and filling into plastic pots (the diameter is 14.5cm, the height is 11.5cm), wherein 1.5kg of soil is filled in each pot. And (4) selecting healthy strawberry seedlings with consistent sizes for transplanting, wherein 1 strawberry seedling is planted in each pot, and managing according to conventional water and fertilizer measures.

Inoculation: the spores of phytophthora which have a diameter of 90cm and are cultured for 10 days on a PDA plate at 25 ℃ are scraped to prepare a spore suspension, the spore suspension is uniformly mixed, 10 parts of the spore suspension are divided into 100mL parts, 20g of the solid microbial agent II prepared in the above examples 4-1, 4-2, 4-3, 4-4 and comparative examples 4-1, 4-2, 4-3, 4-4 and 4-5 are respectively and uniformly mixed with 1 part of the spore suspension to prepare a mixed solution, and sterile water and the spore suspension are uniformly mixed to serve as a control solution CK. And after the strawberry seedlings are transplanted for 5 days, inoculating the mixed solution and the reference solution CK by adopting a perfusion method, wherein each treatment corresponds to 3 pots of strawberry seedlings, and each pot is inoculated with 100 mL. And (4) carrying out normal management in the later period, digging out plants after 1 month of inoculation, counting the disease degree, calculating the disease index, and obtaining the control effect, wherein the treatment result is shown in a table 9.

TABLE 9

Note: 1. incidence rate (number of diseased plants/total number of plants) × 100%; 2. the disease index ∑ (number of each disease-level strain × representative level value)/(total number of strains × representative level value at the highest level of morbidity) × 100; 3. the prevention and treatment effect is [ control disease index-treatment disease index)/control disease index ] x 100%; 4. disease grading standard: grade 0, healthy root; grade I, the lower lateral roots of 1/5 are rotten; grade II, 1/5-1/3 lateral root rot; grade III, 1/3 to 2/3 lateral root rot; grade IV, rotting of lateral roots above 2/3 and even death of the whole plant

As can be seen from table 9, in the laboratory experiment of strawberry potting, the control effect of example 4-1 on strawberry root rot is the best, and the mixed use of glucose, soybean meal, potassium fulvate and 2501 solid microbial agent I produces a certain synergistic effect, and the control effect on fusarium oxysporum is significant.

Effect examples 4 to 3

1500g of soil sample is weighed and evenly mixed with 5g of microbial inoculum prepared in the examples 4-1, 4-2, 4-3, 4-4 and the comparative examples 4-1, 4-2, 4-3, 4-4 and 4-5 respectively, the treatment which is not mixed with the microbial inoculum is used as a control, each treatment is repeated for 3 times, 10 heads of grub larvae with 2 ages are inoculated in each repetition, and the grub larvae are raised and observed under the test conditions of 25 +/-1 ℃ and relative humidity of 60-80%. The grub death condition was investigated 72h after the treatment. The death criteria were judged to be that the worm body had contracted significantly or that the needle had failed to crawl normally, and the results are shown in Table 10.

Watch 10

Treatment of	Death rate of grubs%
		Example 4-1	80
Example 4 to 2	60
		Examples 4 to 3	50
Examples 4 to 4	50
		Comparative example 4-1	48
Comparative examples 4 to 2	40
		Comparative examples 4 to 3	40
Comparative examples 4 to 4	50
		Comparative examples 4 to 5	10
Sterile water	10

As is clear from Table 10, the solid microbial preparation prepared in example 4-1 showed the highest lethality against grubs.

Application example 1

The 2501 solid microbial agent II prepared in example 4-1 is used for controlling red-rooted root rot of strawberry, and comprises the following steps:

the use place is as follows: wangchun town strawberry growing area in Linyi lan mountain area.

The selection takes place the serious plot of red center pillar root rot of strawberry, utilizes the different dilution concentration of microbial inoculum to irritate the root to the strawberry that takes place red center pillar root rot, looks over the prevention and cure condition of strawberry root rot, and six processings are established altogether in the experiment: 50 times of microbial agent, 100 times of microbial agent, 200 times of microbial agent, 300 times of microbial agent, 500 times of microbial agent and sterile water contrast; each treatment was repeated 3 times, randomized block permutation.

The use period is as follows: the seedling is transplanted once, the using amount is 200 mL/plant, then the seedling is used once every 12 days, the using amount is 200 mL/plant, then the seedling is used once every 15 days, the using amount is 300 mL/plant, the using amount is 3 times in total in the whole growing season, and the root irrigation using amount is consistent in each treatment.

Investigation and statistics: 15d after the three-time bactericide application, the number of diseased plants and healthy plants and the disease degree of roots of each treatment group were investigated, and the results are shown in Table 11.

TABLE 11

Treatment of	The incidence of disease%	Index of disease condition	The control effect is%
				50 times of microbial agent	12.72±0.25a	12.05±0.5a	87.56±1.87a
100 times of microbial agent	16.22±0.4b	14.87±0.75b	81.17±1.56b
				200 times of microbial agent	28.37±0.51c	24.49±0.7c	71.22±1.33c
300 times of microbial agent	34.16±1.12c	29.69±1.2c	67.25±1.59c
				500 times of microbial agent	56.8±1.05d	46.15±1.25d	43.54±1.37d
CK sterile water	94.55±0.8e	77.98±1.05e	---

As can be seen from Table 11, after the root is irrigated by using 2501 solid microbial inoculum II, the solid microbial inoculum has different control effects on red stele root rot of strawberry, the morbidity and the disease index increase with the increase of the dilution factor, and the control effect decreases with the increase of the dilution factor; the contrast morbidity of the sterile water is more than 94 percent, the effect is obvious when the sterile water is used for 300 times of liquid, particularly when the sterile water is used for 100 times of liquid, the disease can be basically controlled not to occur, and the control effect is lower than 50 percent when the sterile water is diluted for 500 times.

Application example 2

The 2501 preparation of solid microbial inoculum II for controlling sunflower sclerotinia sclerotiorum by using the method in the example 4-1 comprises the following steps:

the use place is as follows: sunflower field of Sara flag of inner Mongolia Baotou

Selecting a land parcel with serious sunflower sclerotiniose, diluting the land parcel with a microbial agent by a certain multiple to perform root irrigation treatment on the sunflower, and using the land parcel for three times, wherein the land parcel is 200 mL/plant in the seedling stage and is used for 15 days at intervals, the land parcel is used for the second time, the land parcel is used for the third time at intervals of 20 days, and the land parcel is used for the third time, and the land parcel is used for 500 mL/plant; the experiment is provided with five treatments, namely 50 times of solution of microbial agent, 100 times of solution of microbial agent, 200 times of solution of microbial agent, 500 times of solution of microbial agent and sterile water control, the treatment is repeated three times, and the treatments are arranged in random blocks; the number of plants affected by each treatment was investigated in the flowering phase when water stain white hyphae appeared as a control, and the incidence and control effect were calculated, and the results are shown in table 12.

TABLE 12 prevention and control effect of different usage amounts of microbial agents on sunflower

Treatment of	The incidence of disease%	The control effect is%
			50 times of microbial agent	8.37±0.25a	79.22±1.87a
100 times of microbial agent	14.15±0.4b	71.17±1.56b
			200 times of microbial agent	38.80±1.05c	49.66±1.33c
500 times of microbial agent	61.23±1.05d	25.57±1.37d
			CK sterile water	94.55±0.8e	—

Note: 1. incidence rate (number of diseased plants/total number of plants) × 100%; 2. control effect is (control morbidity-treatment morbidity)/control morbidity x 100%;

a, the difference is not significant; b significant difference

As can be seen from table 12, after the roots are irrigated with 2501 solid microbial inoculum, the control effect on sunflower sclerotinia rot is different, the morbidity and disease index increase with the increase of the dilution factor, and the control effect decreases with the increase of the dilution factor. The contrast morbidity of the sterile water is more than 94 percent, the effect is obvious when the sterile water is used for 100 times of the diluent, and the control effect is poor and is less than 50 percent when the sterile water is used for 200 times of the diluent.

Application example 3

The method for preventing and controlling the apple leafroller by utilizing the 2501 liquid microbial agent II prepared in the embodiment 3-1 comprises the following steps of:

the use place is as follows: town three village apple orchard of Shandong Penglai Daxin shop

The test is totally provided with six treatments: 50 times of microbial agent, 100 times of microbial agent, 200 times of microbial agent, 300 times of microbial agent, 500 times of microbial agent and sterile water contrast; each treatment is repeated 4 times, and the treatment is carried out in 24 cells in total, and the treatment is randomly arranged in blocks, and each cell contains 4 fruit trees. The overwintering generation larva is carried out in the early stage (4 middle ten days of the month), the field is sprayed for 2 times, and the 2 nd full-tree spraying is carried out 10 days after the 1 st pesticide application, so that all pesticides are uniformly applied to the tree crowns, and the average pesticide application amount of each plant is 4L.

Investigation and statistics: before application, the population base number is investigated, 2 plants are randomly selected for each treatment, one branch is marked in the east, west, south, north and middle directions of each plant, and the sizes of the marked branches are as consistent as possible. After the application, the number of live insects per marker strain was investigated at 5d, 10d and 14d, respectively, and the results are shown in Table 13

Watch 13

5. Control effect (%) - (reduction rate of population in medicament treatment area-reduction rate of population in blank control area)/(reduction rate of population in 100-blank control area) x 100

a, the difference is not significant; b significant difference

From table 13, the control effect of 2501 liquid microbial inoculum ii on spodoptera frugiperda is known as follows: the microbial agent is diluted to 50, 100 and 200 times for application, and the control effect difference of the microbial agent on the spodoptera frugiperda is not obvious, and the using effect is obvious. When the pesticide is diluted to more than 500 times, the insecticidal effect is poor, the control effect is below 50 percent, and the use by diluting below 200 times is recommended.

Application example 4

The prevention and treatment of the wheat thrips tuba by using the 2501 liquid microbial agent II prepared in the embodiment 3-1 comprises the following steps:

the use place is as follows: shandong chapter hill area Gaoyouzhai Zhengzhen wheat field

The test is totally provided with six treatments: 50 times of microbial agent, 100 times of microbial agent and 200 times of microbial agent300 times of microbial agent, 500 times of microbial agent and sterile water contrast; each treatment was repeated 3 times for 18 cells in a random block arrangement, each cell having an area of 20m². Spray treatment of stem and leaf is carried out in the booting stage of wheat, and each plot is 900 ml.

Investigation and statistics: before application, the population base is investigated, 5 points are sampled from each plot, 10 plants are fixed and marked at each point, and the number of thrips on the plants (ears) is investigated and recorded. The number of live insects of the marker strain was investigated 12 hours, 24 hours, and 48 hours after the application, and the results of the treatment are shown in Table 14.

TABLE 14

2. Control effect (%) - (reduction rate of population in drug-treated area-reduction rate of population in blank control area)/(reduction rate of population in 100-blank control area) × 100

a, the difference is not significant; b significant difference

As can be seen from table 14, the control effect of microbial agent ii prepared from 2501 on wheat thrips griffithii is known: the microbial agent is diluted to 50, 100, 200 and 300 times for application, and has the advantages of insignificant difference in prevention and treatment effects on wheat straw thrips and the best use effect. When the pesticide is diluted to more than 500 times, the insecticidal effect is poor, the control effect is below 45 percent, and the use by diluting below 300 times is recommended.

Plant pathogenic fungi (fusarium oxysporum, phytophthora parasitica and sclerotinia sclerotiorum), spodoptera exigua and thrips horrida are taken as targets, the orange subspecies of the pseudomonas chlororaphis of a microbial strain with the sterilization function and the insecticidal function is screened, the blank that the pseudomonas chlororaphis only has a single biocontrol function is filled, and a good effect is obtained through a field application experiment. Compared with the conventional microbial inoculum and chemical pesticide, the microbial inoculum containing the green needle pseudomonas orange subspecies has the following advantages: through practical tests, the bactericide has obvious control effects on plant pathogenic fungi (fusarium oxysporum, phytophthora, sclerotinia sclerotiorum), apple cabbage loopers, thrips gramineara and grubs, and can improve the control effects compared with the conventional bactericide discovered at present; the bactericidal spectrum and the insecticidal spectrum are wide, one agent is multi-purpose, and can replace part of conventional bactericides, so that the workload is reduced, and the cost is reduced; high efficiency and environmental protection, can reduce the use of chemical pesticides, reduce the occurrence of drug resistance, is beneficial to environmental protection and comprehensive treatment, and has important significance for agricultural production.

Claims

1. The solid microbial agent II of the pseudomonas chlororaphis orange subspecies 2501 is characterized by comprising the following components in parts by weight: 20-30 parts of glucose, 15-25 parts of soybean meal, 25-35 parts of potassium fulvate and 10-30 parts of pseudomonas chlororaphis orange subspecies 2501 solid microbial agent I; the Pseudomonas chlororaphis orange subspecies 2501 solid microbial agent I is a fermentation liquid prepared by liquid fermentation of Pseudomonas chlororaphis orange subspecies 2501, the fermentation liquid is dried to prepare the Pseudomonas chlororaphis orange subspecies 2501 solid microbial agent I, and the effective viable count of the Pseudomonas chlororaphis orange subspecies 2501 solid microbial agent I is 2 multiplied by 10¹¹cfu/g or more;

pseudomonas chlororaphis subsp. aurantiaca 2501, deposited in China general microbiological culture Collection center on 6.2.2020, with the deposition address: the No. 3 Xilu No.1 of Beijing, Chaoyang, the preservation number is CGMCC NO. 19900.

2. The process for producing a solid microbial preparation I of Pseudomonas chlororaphis orange subspecies 2501 in the solid microbial preparation II of Pseudomonas chlororaphis orange subspecies 2501 of claim 1, which comprises the steps of:

(5) inoculating the third-level seed liquid prepared in the step (4) into a liquid fermentation culture medium, wherein the inoculation amount is 5-10% by volume; the culture temperature is 30 +/-0.5 ℃, the culture time is 28-32h, the rotation speed is 100-150rpm, and the ventilation volume is 0.8-1.2vvm, so as to prepare a liquid fermentation product, namely the pseudomonas chlororaphis orange subspecies 2501 liquid microbial agent I;

3. The solid microbial inoculant II of pseudomonas chlororaphis orange subspecies 2501 of claim 1, wherein the solid microbial inoculant II of pseudomonas chlororaphis orange subspecies 2501 comprises the following components in parts by weight: 30 parts of glucose, 20 parts of soybean meal, 30 parts of potassium fulvate and 20 parts of pseudomonas chlororaphis orange subspecies 2501 solid microbial agent I.

4. The method of claim 2,

the solid culture medium of the step (1) comprises the following components: 10g/L of tryptone, 5g/L of yeast powder, 10g/L of sodium chloride, 5g/L of glucose, 18-20g/L of agar and the balance of water, wherein the pH value is 7.0-7.2;

preferably, the composition of the primary liquid seed culture medium in step (2) is as follows: 10g/L of tryptone, 5g/L of yeast powder, 10g/L of sodium chloride, 5g/L of glucose and the balance of water, wherein the pH value is 7.0-7.2;

preferably, the rotation speed in the step (2) is 190-200rpm, and the culture time is 22-24 h;

preferably, the composition of the secondary seed liquid culture medium in step (3) is as follows: 10g/L of tryptone, 5g/L of yeast powder, 10g/L of sodium chloride, 5g/L of glucose and the balance of water, wherein the pH value is 7.0-7.2;

preferably, the inoculation amount in the step (3) is 3.5-5 per mill by volume fraction, the culture temperature is 30 +/-0.5 ℃, the culture time is 14-15h, the rotation speed is 220-;

preferably, the components of the tertiary seed liquid culture medium in the step (4) are as follows according to mass fraction: pancreatic bean pulp 0.2%, corn flour 1%, glucose 1%, peptone 0.5%, magnesium sulfate 0.1%, ammonium sulfate 0.1%, potassium dihydrogen phosphate 0.05%, dipotassium hydrogen phosphate 0.05%, and balance water, wherein the pH value is 7.2-7.5;

preferably, the inoculation amount in the step (4) is 6-10% by volume fraction, the culture temperature is 30 +/-0.5 ℃, the culture time is 7-9h, the rotation speed is 160-.

5. The method as claimed in claim 2, wherein the volume fraction of the inoculum in step (5) is 6-10%, the incubation temperature is 30 ± 0.5 ℃, the incubation time is 29-32h, the rotation speed is 130-150rpm, and the aeration rate is 1.0-1.2 vvm;

preferably, the liquid fermentation medium in step (5) has the following composition: 1% of soybean meal, 3% of corn flour, 1% of glucose, 0.5% of peptone, 0.2% of magnesium sulfate, 0.3% of ammonium sulfate, 0.1% of monopotassium phosphate, 0.1% of dipotassium phosphate and the balance of water, wherein the pH value is 7.2-7.5.

6. The method of claim 2, wherein the drying method in step (6) is a spray drying method.

7. A method of preparing solid microbial inoculant II of pseudomonas aeruginosa orange subspecies 2501 as claimed in claim 1 or 3, comprising the steps of:

uniformly mixing 20-30 parts by weight of glucose, 15-25 parts by weight of soybean meal, 25-35 parts by weight of potassium fulvate and 10-30 parts by weight of solid microbial agent I of the orange subspecies 2501 of the pseudomonas chlororaphis to prepare the solid microbial agent II of the orange subspecies 2501 of the pseudomonas chlororaphis.

8. The method of claim 7, comprising the steps of:

the components in parts by weight are as follows: 30 parts of glucose, 20 parts of soybean meal, 30 parts of potassium fulvate and 20 parts of pseudomonas chlororaphis orange subspecies 2501 solid microbial agent I are uniformly mixed to prepare the pseudomonas chlororaphis orange subspecies 2501 solid microbial agent II.

9. Use of the solid microbial inoculant II of pseudomonas chlororaphis subsp. aurantia 2501 of any one of claims 1 or 3 for biological control of crops.

10. The use of claim 9, wherein the pseudomonas chlororaphis subsp. aurantia 2501 solid microbial agent II is used for controlling fungal diseases and insect pests of crops.