CN105462893A

CN105462893A - Application of sophora tonkinensis endophytic bacterium B29 in preventing and controlling panax notoginseng root rot

Info

Publication number: CN105462893A
Application number: CN201510979400.6A
Authority: CN
Inventors: 黄荣韶; 乔云明; 姚裕群; 李良波
Original assignee: Guangxi University
Current assignee: Guangxi University
Priority date: 2015-12-23
Filing date: 2015-12-23
Publication date: 2016-04-06
Anticipated expiration: 2035-12-23
Also published as: CN105462893B

Abstract

The invention discloses a sophora tonkinensis endophytic bacterium B29. The sophora tonkinensis endophytic bacterium B29 is classified and named as Burkholderia sp. B29, wherein the 16S rDNA gene sequence table of the strain is as described by SEQ ID NO.1, the depository authority is the General Microbiological Collection Center of China Committee for Culture Collection of Microorganisms, the depository address is Institute of Microbiology, Building 3, No.1, Beichen West Road, Chaoyang District, Beijing, the depository date is 13 May 2015, and the depository number is CGMCC No.10807. According to the sophora tonkinensis endophytic bacterium B29 provided by the invention, a strain of endophytic bacterium Burkholderia sp. B29 is separated and screened from the root of a medicinal plant sophora tonkinensis for the first time, the Burkholderia sp. B29 has a strong inhibiting effect on panax notoginseng fusarium solani, and a wide application prospect is created for the biological prevention and control field of panax notoginseng fungal diseases.

Description

The application of sophora tonkinensis Gapnep endogenetic bacteria B29 in control notoginseng root rot

Technical field

The present invention relates to biological technical field, the particularly application of a kind of sophora tonkinensis Gapnep endogenetic bacteria B29 in control notoginseng root rot.

Background technology

The control of modern agriculture to Plant diseases is overly dependent upon the use of chemical pesticide, discharging of a large amount of chemical pesticide not only has long-term destruction to ecotope, also cause quality of agricultural product to decline, pesticide residue exceed standard, the resistance of pathogenic bacteria and to problems such as people and animals are harmful.Find safer, effective pest control method to be significant, utilizing biological method to carry out controlling plant diseases can effectively solve the problem.

Pseudo-ginseng (PanaxnotoginsengF.H.chen) has another name called pseudo-ginseng, invaluable etc., and having promoting blood circulation and removing blood stasis, subduing swelling and relieving pain effect significantly, is a kind of Chinese tradition rare medicinal herbs.Be that the Chinese patent medicine that main raw material is made is as wide-spread in " Yunnan white powder " and " Pien Tze Huang " etc. with pseudo-ginseng.In recent years, growing to the raw-material demand of pseudo-ginseng.But the fungal disease in cultivation has had a strong impact on Panax notoginseng Growth.At present, on notoginseng planting, control fungal disease depends on chemical pesticide unduly, and the use of a large amount of chemical pesticide not only have impact on the quality of pseudo-ginseng, also result in a large amount of pesticide residue of pseudo-ginseng.

Notoginseng root rot is one of pseudo-ginseng Major Diseases, is commonly called as " green smelly " in producing region, and cardinal symptom is that the bud-rot in seedling stage and the brown water stain shape pathology of reed head and bastem junction thereof are until spread to whole cane base portion.Just there is generation in this disease seeding stage, 4, May disease stagnate, the 6-9 month enters rainy season, enters onset peak period.Root rot has broad variety, it is reported that its symptom is mostly caused by notoginseng root rot bacterium (Fusariumsolani) (being called for short F.solani).

This fungal disease is the one of the main reasons causing pseudo-ginseng quality product and production declining for many years.In traditional Genuine producing area of Guangxi pseudo-ginseng, due to the meteorological conditions of low altitude area and high temperature and humidity, this disease is simultaneous often, and a large amount of underproduction causing pseudo-ginseng are even had no harvest, and brings huge financial loss to plantation family.In order to control this fungal disease, a large amount of chemical pesticides is used, and cause a large amount of pesticide residue of pseudo-ginseng product, serious pollutes environment, has threatened the health of people greatly.Therefore, it is very urgent and necessary for carrying out the Sustainable development of biological control pseudo-ginseng fungal disease to pseudo-ginseng industry.Filter out for this reason and can the Antagonistic Fungi of simultaneously this disease of antagonism be significant, screening and then to develop Antagonistic Fungi be also effectively control one of the most potential prophylactico-therapeutic measures of pseudo-ginseng fungal disease.

The information being disclosed in this background technology part is only intended to increase the understanding to general background of the present invention, and should not be regarded as admitting or imply in any form that this information structure has been prior art that persons skilled in the art are known.

Summary of the invention

The object of the present invention is to provide the application of a kind of sophora tonkinensis Gapnep endogenetic bacteria B29 in control notoginseng root rot, thus the notoginseng root rot occurred in energy effectively preventing notoginseng planting process, thus improve output and the quality of pseudo-ginseng.

For achieving the above object, technical scheme provided by the invention is as follows:

A kind of sophora tonkinensis Gapnep endogenetic bacteria B29, the Classification And Nomenclature of sophora tonkinensis Gapnep endophyte B29 is bulkholderia cepasea (Burkholderiasp.) B29, the 16SrDNA gene order table of bacterial strain is as described in SEQIDNO.1, depositary institution: China Committee for Culture Collection of Microorganisms's common micro-organisms center, preservation address: No. 3, Yard 1, BeiChen xi Road, Chaoyang District, Beijing City Institute of Microorganism, Academia Sinica, preservation date: on 05 13rd, 2015, preserving number: CGMCCNo.10807.

Preferably, the preparation method of described sophora tonkinensis Gapnep endogenetic bacteria B29 meta-bolites is: be inoculated in NB liquid nutrient medium by sophora tonkinensis Gapnep endogenetic bacteria B29, be placed in that temperature is 28 DEG C, rotating speed is that 130r/min condition bottom fermentation cultivates 10 days, the ultrasonic 40min of gained fermented product, then 2 times are extracted with ethyl acetate, get ethyl acetate and carry out the ethyl acetate extract that concentrating under reduced pressure obtains strain fermentation thing mutually, be sophora tonkinensis Gapnep endogenetic bacteria B29 meta-bolites.

Preferably, described sophora tonkinensis Gapnep endogenetic bacteria B29 is inoculated in containing 1000mlNB liquid nutrient medium.

Preferably, described NB liquid nutrient medium is containing beef extract 3g, yeast extract paste 1g, peptone 5g, sucrose 10g, and Medium's PH Value is 7.0.

The application of meta-bolites in control notoginseng root rot of gained sophora tonkinensis Gapnep endogenetic bacteria B29 is prepared as above-mentioned.

Compared with prior art, the present invention has following beneficial effect:

The present invention first from the root of medicinal plant sophora tonkinensis Gapnep separation screening to strain endogenetic bacteria (Burkholderiasp.) B29, this bacterium has very strong restraining effect to notoginseng root rot bacterium, and the field of biological control for pseudo-ginseng fungal disease brings wide application prospect.

Accompanying drawing explanation

Fig. 1 is the dull and stereotyped opposite culture of sophora tonkinensis Gapnep endogenetic bacteria B29 of the present invention and notoginseng root rot, and wherein F is notoginseng root rot bacterium (Fusariumsolani), a is blank, and b is experimental group.

Fig. 2 is sophora tonkinensis Gapnep endogenetic bacteria B29 strain morphology feature of the present invention, and wherein, a1 is colonial morphology, and b1 is thalli morphology.

Fig. 3 is the phylogenetic tree that sophora tonkinensis Gapnep endogenetic bacteria B29 bacterial strain builds based on 16SrDNA gene order.

Fig. 4 is to the inhibition of the mycelial growth of notoginseng root rot bacterium according to the meta-bolites of bacterial strain sophora tonkinensis Gapnep endogenetic bacteria B29 of the present invention; Wherein the 1st, the 5th is that namely the PDA of pastille is not dull and stereotyped for blank; 2nd, the 3rd, the 4th is positive control powder of carbendazim; 6th, the 7th, the 8th is the meta-bolites of bacterial strain B29, and concentration is respectively 2mg/ml, 4mg/ml, 8mg/ml; F is notoginseng root rot bacterium Fusariumsolani.

Embodiment

Be described in detail below in conjunction with embodiment, but be to be understood that protection scope of the present invention not by the restriction of embodiment.The experimental technique used in following embodiment if no special instructions, is ordinary method.The material used in following embodiment, reagent etc., if no special instructions, all can obtain from commercial channels.Ethyl acetate is commercial analytical pure ethyl acetate.2XTagMasterMix is purchased from precious biotechnology company limited (Takara), and Primer-1, Primer-2 are by Hua Da gene chemical synthesis.

Embodiment 1

The separation of bacterial strain, screening and qualification

One, the separation of bacterial strain

For examination material: the wild sophora tonkinensis Gapnep picking up from In Limestone Area, Tiandeng County, Guangxi.

Strains tested: provided by plant pathology institute of Guangxi University.

Substratum: 1000mlNA substratum: beef extract 3g, yeast extract paste 1g, peptone 5g, sucrose 10g, agar 15g, pH7.0.

Surface sterilization: by long for 6-8cm, the wide sophora tonkinensis Gapnep root running water 30min for 1-2cm fresh and healthy are to rinse silt, then the sophora tonkinensis Gapnep root rinsed with sterile water 2 times will cleaned, air-dry surface-moisture, moving on to Bechtop, aseptically, is 75% alcohol immersion 1min by sophora tonkinensis Gapnep root volumetric concentration, rinsed with sterile water 2 times, clorox (available chlorine 1%) soaks 2min, aseptic washing 3 times, and it is for subsequent use that aseptic thieving paper blots surface.

The separation of bacterial strain, purifying: the sophora tonkinensis Gapnep root that surface sterilization is good, under aseptic condition, epidermis is scraped off with aseptic wood chip, the two ends of sophora tonkinensis Gapnep root are cut off with aseptic secateurs, remaining part aseptic pocket knife and aseptic nipper separate xylem and phloem, get the tissue block that 0.5cm is long respectively, shred and add sterilized water grinding with aseptic secateurs, add sterilized water after grinding be fully settled to 5ml and leave standstill 10min, get 0.5ml supernatant liquor gradient dilution 10 ~ 10 ⁵doubly, get 100 μ L diluents respectively and be applied on NA flat board, each weaker concn repeats 3 times, gets last rinsing liquid and is coated on NA flat board, as negative control.NA flat board is placed in incubator 28 DEG C of constant temperature culture 24 ~ 96h, and picking different shape bacterium colony is rule purifying repeatedly, the bacterial strain of purifying and sophora tonkinensis Gapnep endogenetic bacteria 20% glycerine is preserved.

The sophora tonkinensis Gapnep endogenetic bacteria be separated to is inoculated on LA flat board, stand-by after cultivating 24h at 28 DEG C.Notoginseng root rot bacterium is inoculated in PDA flat board, cultivates after 3 days stand-by at 28 DEG C.

Two, screen

Adopt dull and stereotyped face-off method to the primary dcreening operation carrying out thalline bacteriostatic activity for examination sophora tonkinensis Gapnep endogenetic bacteria.

First, under aseptic condition, with sterilizing punch tool, notoginseng root rot bacterium is made 6mm bacterium cake; In treatment group, notoginseng root rot bacterium bacterium cake is transferred to the culture dish central authorities containing NA, then in the position of distance bacterium cake 2cm, the sophora tonkinensis Gapnep endogenetic bacteria bacterial strain be separated to is connected a bacterium line, and every strain endogenetic bacteria repeats 3 wares; In control group, only connect notoginseng root rot bacterium bacterium cake, do not connect sophora tonkinensis Gapnep endogenetic bacteria, repeat 3 wares.Then, cultivate at 28 DEG C, periodic observation.When fungi covers with culture dish in control group, in treatment group, measure the growth radius of notoginseng root rot bacterium between notoginseng root rot Jun Junbing center to sophora tonkinensis Gapnep endogenetic bacteria line center for process growth radius; In control group, the growth radius of notoginseng root rot bacterium is contrast growth radius.Finally, according to following formula, calculate bacteriostasis rate:

Contrast increment=contrast growth radius-bacterium cake radius

Process increment=process growth radius-bacterium cake radius

Result obtains the 3 strains antagonism sophora tonkinensis Gapnep endogenetic bacteria bacterial strain all very strong to notoginseng root rot bacterium restraining effect altogether, and wherein a strain name is called B29, is 71% to the inhibiting rate of notoginseng root rot bacterium.

Three, identify

(1) strain morphology feature

Colony morphology characteristic is observed: by inoculation to be identified on NA substratum, is placed in 28 DEG C and cultivates 24h, observe the colony morphology characteristic of bacterial strain.

Morphological features is observed: get the above-mentioned bacterial strain cultivating 24h on NA substratum and carry out gramstaining and microscopy, by the photomicrography of viewed form result, as shown in Figure 2.

(2) bacterial strain 16SrDNA sequence and phylogenetic analysis thereof

The preparation of DNA profiling:

Reagent: (1) lysis buffer: Tris-Ac (pH7.8) 40mM, NaAc20mM, EDTA1mM, SDS1% (w/v);

(2) 5MNaCl solution.

DNA extraction:

A 1.5ml overnight bacterial nutrient solution culture is placed in Eppendorf tube (EP pipe) by (), the centrifugal 0.5min of 12000rpm, abandoning supernatant, retains throw out;

B () adds 400 μ l lysis buffers in throw out, repeatedly blow and beat make it resuspended with suction pipe;

C () adds 200ul5MNaCl, fully mix, the centrifugal 10min of 12000rpm, gets 600 μ l supernatant liquors;

D () adds isopyknic phenol/chloroform (1:1), mixing, and centrifugal (12000rpm, 10min), proceeds in another clean EP pipe by supernatant liquor;

Add equal-volume chloroform in e supernatant liquor that () obtains in step (d), mixing, centrifugal (12000rpm, 10min), proceeds in another clean EP pipe by supernatant liquor;

F () adds isopyknic Virahol in gained supernatant liquor in step (e), mixing, is placed in room temperature 10min, centrifugal (12000rpm, 15min), abandoning supernatant, retains throw out;

G () is 70% washing with alcohol step (f) gained throw out by volumetric concentration, dry, be DNA;

H DNA dry in step (g) is dissolved in 30 μ l distilled water (ddH by () ₂o) in ,-20 DEG C of preservations.

Pcr amplification 16SrDNA sequence:

(1) PCR instrument: ABI3730-XLDNA sequenator (AppliedBiosystems, USA);

(2) amplimer: 27F (5 '-AGAGTTTGATCCTGGCTCAG-3 ') is as shown in SEQIDNO.2, and 1492R (5 '-GGTTACCTTGTTACGACT-3 ') is as shown in SEQIDNO.3;

(3) amplification system:

16SrDNA sequence PCR amplification system is as shown in table 1:

Table 1.

Reactant	Application of sample amount
		2X TagMasterMix	25μL
Primer-1	1μL
		Primer-2	1μL
Template DNA	0.5μL
		ddH ₂O	22.5μL
Reaction cumulative volume	50μL

Note: the TemplateDNA in table 1 is that above-mentioned steps (h) gained DNA makes DNA profiling.

PCR reaction conditions is as shown in table 2:

Table 2.

Note: in table 2, step 2 carries out 30 circulations.

The electrophoresis detection of pcr amplification product:

Deposition condition is the sepharose (containing Goldview5 μ l/100ml) of 1%, 1 × TBE electrophoretic buffer, 90V electrophoresis 1 hour, and PCR primer applied sample amount is 3 μ L, point sample after mixing with 1 μ LLoadingdye.Observations under 254nm ultraviolet, with the DL1000DNAMarker of TaKaRa company for nucleic acid standard molecular weight object of reference, determines expanding fragment length.Amplified production band should on the position of standard substance 400-700bp.

PCR primer purifying and order-checking: undertaken by Shenzhen Huada Genetic Technology Co., Ltd.

The structure of systematic evolution tree:

The 16SrDNA sequence of the bacterium measured in surveyed 16SrDNA sequence and GenBank gene pool is compared, recalls the 16SrDNA sequence of the bacterial strain higher with its sequence homology.Adopt Clustal-W software to carry out mating arrangement to homologous sequence more, carried out the constructing system evolutionary tree of systematic evolution tree by MEGA6.0 software, as shown in Figure 3.

Result:

(1) strain morphology feature

Colony morphology characteristic: bacterial strain bacterium colony is in yellow-green colour on NA flat board, and smooth surface, protuberance, neat in edge, circular, on NA flat board, cultivation 5 days diameters are 1-2mm, as shown in a1 in Fig. 2.

Morphological features: Gram-negative is negative staining, without gemma, thalline direct rod shape, size is (0.41 ~ 0.45) μm × (0.96 ~ 1.29) μm, as shown in b1 in Fig. 2.

(2) bacterial strain 16SrDNA sequence and phylogenetic analysis thereof

Utilize primer 2 7F and 1492R, the fragment of a 1300-1400bp is amplified from strain gene group DNA, through checking order and by sequencing result by BLASTn comparison in GenBank, utilizing the adjacent algorithm (Neighbor-joiningNJ) of MEGA6 to carry out systems analysis and constructing system evolutionary tree.Result shows, 16SrDNA sequence and the corresponding sequence homology of Burkholderiasp.SAP27_1 reach 99%.Comprehensive morphological and molecular biological characteristics, be initially identified as Burkholderiasp. by bacterial strain.Embodiment 2

Sophora tonkinensis Gapnep endogenetic bacteria B29 meta-bolites is to the restraining effect of notoginseng root rot bacterium

One, the fermentation culture of bacterial strain and the extraction of meta-bolites

Sophora tonkinensis Gapnep endogenetic bacteria B29 is inoculated in containing 1000mlNB liquid nutrient medium (beef extract 3g, yeast extract paste 1g, peptone 5g, sucrose 10g, pH7.0) in 2 liters of Erlenmeyer flasks, be placed in the shaker fermentation that temperature is 28 DEG C, rotating speed is 130r/min and cultivate 10 days, gained fermented product ultrasonic echography 40min, then 2 times are extracted with ethyl acetate, get the ethyl acetate extract that twice gained ethyl acetate phase concentrating under reduced pressure obtains strain fermentation thing, be sophora tonkinensis Gapnep endogenetic bacteria B29 meta-bolites.

Two, sophora tonkinensis Gapnep endogenetic bacteria B29 meta-bolites is to the restraining effect of the mycelial growth of notoginseng root rot bacterium

The ethyl acetate extract measuring bacterial strain by mycelial growth method is sophora tonkinensis Gapnep endogenetic bacteria B29 meta-bolites, to the inhibit activities of notoginseng root rot bacterium mycelial growth.The pastille meta-bolites of bacterial strain B29 and powder of carbendazim (positive control) made respectively containing the meta-bolites of 2mg/mL, 4mg/mL, 8mg/mL concentration B29 is dull and stereotyped.Aseptically, with punch tool, pathogenic fungi is made 6mm bacterium cake, it is process that notoginseng root rot bacterium bacterium cake is received the dull and stereotyped central authorities of each pastille, and the notoginseng root rot bacterium bacterium cake connect with not dull and stereotyped central authorities of pastille is for negative control, in triplicate, all flat boards are placed in 28 DEG C of cultivations for all process and contrast.The Field information concentration that drug level presses powder of carbendazim is arranged.When negative control covers with culture dish, measure the growth diameter of contrast bacterium colony and process bacterium colony respectively, and according to following formula, calculate inhibiting rate:

Negative control increment=negative control growth diameter-bacterium cake diameter

Process increment=process growth diameter-bacterium cake diameter

Three, sophora tonkinensis Gapnep endogenetic bacteria B29 meta-bolites is to the minimal inhibitory concentration of notoginseng root rot bacterium

With the meta-bolites of broth dilution method determination bacterial strain B29 to the minimal inhibitory concentration of notoginseng root rot bacterium.PDA is cultivated the notoginseng root rot bacterium pure culture biscuits involvng inoculation of 5 days in the PDB liquid nutrient medium containing 0.2% tween 80 (v/v), 28 DEG C, 150r/min shaking table cultivates 7 days, then culture is forwarded to triangular flask, and the aseptic double-distilled water poured into containing 0.2% tween 80, stir 30min with magnetism stick, solution sterile gauze is filtered, obtain spores solution, and with blood counting chamber, spore concentration is adjusted to every milliliter 10 ⁴individual spore is for subsequent use.The meta-bolites 1%DMSO of bacterial strain B29 is dissolved into the meta-bolites concentration for the treatment of of 80mg/mL, getting 5 sterile test tube is sequentially arranged on test-tube stand, be numbered 1,2,3,4,5 respectively, often pipe adds the aseptic double-distilled water of 1ml containing 0.2% tween 80 respectively, is then added by the meta-bolites solution of the bacterial strain of 1ml80mg/mL in the test tube being numbered 1 and also in each pipe, carries out twice serial dilution successively.The above-mentioned gained spores solution (10 of 1ml ⁴individual/ml) add in each pipe respectively, thus obtain the meta-bolites concentration for the treatment of of final B29: 20mg/ml (numbering 1 test tube), 10mg/ml (numbering 2 test tube), 5mg/ml (numbering 3 test tube), 2.5mg/ml (numbering 4 test tube), 1.25mg/ml (numbering 5 test tube).The 8mg/mL Flusilazole of 1%DMSO and 1ml of 1ml replaces the meta-bolites of B29 to perform above-mentioned treating processes respectively and as negative control and positive control, all process and contrast are in triplicate.Finally, each pipe 28 DEG C, 150r/min shaking table cultivates 5 days.The MIC value of the meta-bolites of sophora tonkinensis Gapnep endogenetic bacteria B29 is suppress the minimum crude extract concentration of notoginseng root rot bacterium visible growth completely.

Result:

The percent inhibition of bacterial strain sophora tonkinensis Gapnep endophyte B29 meta-bolites to notoginseng root rot bacterium mycelial growth is as shown in table 3:

Table 3.

Note: show positives contrast powder of carbendazim containing 50% derosal; After in table, * represents that LSD that data pass through one-way analysis of variance is relatively, the meta-bolites of bacterial strain B29 and positive control powder of carbendazim under same concentrations, at P _0.05tool significant difference in level.

The suppression result of meta-bolites to notoginseng root rot bacterium mycelial growth of bacterial strain sophora tonkinensis Gapnep endophyte B29 shows, the meta-bolites of bacterial strain sophora tonkinensis Gapnep endophyte B29 all has extraordinary inhibition to the mycelial growth of notoginseng root rot bacterium, and the percent inhibition of meta-bolites to notoginseng root rot bacterium F.solani mycelial growth of B29 is 71.56-100% as can be seen from Table 3.Compare with positive control powder of carbendazim, the meta-bolites of bacterial strain B29, to the inhibition of notoginseng root rot bacterium F.solani mycelial growth, when concentration is less than or equal to 4mg/mL, a little less than contrast, when concentration 8mg/mL, with contrast equivalent.

The minimal inhibitory concentration of bacterial strain B29 meta-bolites to notoginseng root rot bacteria growing is as shown in table 4:

Table 4.

Process	MIC(mg/ml)
			F.solani
Flusilazole	0.5
		B29	2.5

Note: showing positives contrast Flusilazole active constituent content is 400mg/mL.

The minimal inhibitory concentration test result of meta-bolites to notoginseng root rot bacteria growing of bacterial strain sophora tonkinensis Gapnep endophyte B29 shows, the meta-bolites of bacterial strain sophora tonkinensis Gapnep endophyte B29 all has stronger restraining effect to notoginseng root rot bacterium, the minimal inhibitory concentration of meta-bolites to notoginseng root rot bacterium F.solani of sophora tonkinensis Gapnep endophyte B29 is 2.5mg/ml as can be seen from Table 4, is 5 times of positive control.

As may be known from Table 3 and Table 4, contain the composition of very strong antifungal or fungicidal in the meta-bolites of bacterial strain sophora tonkinensis Gapnep endophyte B29, therefore, in the bionomic control of notoginseng root rot bacterium, bacterial strain sophora tonkinensis Gapnep endophyte B29 has outstanding potentiality.

The aforementioned description to concrete exemplary of the present invention is to illustrate and the object of illustration.These descriptions not want the present invention to be defined as disclosed precise forms, and obviously, according to above-mentioned instruction, can much change and change.The object selected exemplary embodiment and describe is to explain certain principles of the present invention and practical application thereof, thus those skilled in the art can be realized and utilize various different exemplary of the present invention and various different selection and change.Scope of the present invention is intended to limited by claims and equivalents thereof.

Claims

1. a sophora tonkinensis Gapnep endogenetic bacteria B29, is characterized in that: the Classification And Nomenclature of sophora tonkinensis Gapnep endophyte B29 is bulkholderia cepasea (Burkholderiasp.) B29, preserving number: CGMCCNo.10807.

2. the preparation method of the meta-bolites of a sophora tonkinensis Gapnep endogenetic bacteria B29 as claimed in claim 1, it is characterized in that: sophora tonkinensis Gapnep endogenetic bacteria B29 is inoculated in NB liquid nutrient medium, be placed in that temperature is 28 DEG C, rotating speed is that 130r/min condition bottom fermentation cultivates 10 days, the ultrasonic 40min of gained fermented product, then 2 times are extracted with ethyl acetate, get ethyl acetate and carry out the ethyl acetate extract that concentrating under reduced pressure obtains strain fermentation thing mutually, be sophora tonkinensis Gapnep endogenetic bacteria B29 meta-bolites.

3. the preparation method of meta-bolites according to claim 2, is characterized in that: described sophora tonkinensis Gapnep endogenetic bacteria B29 is inoculated in containing 1000mlNB liquid nutrient medium.

4. the preparation method of meta-bolites according to claim 2, is characterized in that: described NB liquid nutrient medium is containing beef extract 3g, yeast extract paste 1g, peptone 5g, sucrose 10g, and Medium's PH Value is 7.0.

5. the application of meta-bolites in control notoginseng root rot preparing gained sophora tonkinensis Gapnep endogenetic bacteria B29 as claim 2.