Pseudomonas protegens inhibiting phomopsis and application of pseudomonas protegens

A technique for Pseudomonas and Phomopsis, which is applied in the field of microorganisms and can solve the problems of few reports on microbial control agents

Active Publication Date: 2019-07-12
INST OF MICROBIOLOGY JIANGXI ACADEMY OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Sun Yanfang and others used 15 kinds of chemical pesticides to carry out indoor screening experiments on asparagus stem blight (Sun Yanfang et al. Determination of the toxicity of 15 kinds of pesticides to the pathogen of asparagus stem blight. 2013,33(4):71-75), Wu Wenneng tested The indoor t

Method used

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  • Pseudomonas protegens inhibiting phomopsis and application of pseudomonas protegens
  • Pseudomonas protegens inhibiting phomopsis and application of pseudomonas protegens
  • Pseudomonas protegens inhibiting phomopsis and application of pseudomonas protegens

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0025] Example 1 Screening of cellulase-producing strains

[0026] Screening medium: CMC-Na10g / L, (NH 4 ) 2 SO 4 1.4g / L, MgSO 4 0.3g / L, KH 2 PO 4 2g / L, MnSO 4 1.6mg / L, FeSO 4 5mg / L, ZnSO 4 2.5mg / L, CoCl 2 2.0mg / L, agar 20g / L, pH7.0

[0027] Seed medium: CMC-Na10g / L, peptone 3g / L, KH 2 PO 4 4g / L, MgSO 4 ·7H 2 O 0.03g / L, pH6.0.

[0028] Fermentation enzyme production medium: CMC-Na10g / L, (NH 4 ) 2 SO 4 4.0g / L, MgSO 4 ·7H 2 O0.5g / L, K 2 HPO 4 2g / L, beef extract 5g / L, peptone 10g / L (natural pH)

[0029] Preliminary screening: Weigh 10g of silt soil sample from the bottom of Qingshan Lake in Nanchang, Jiangxi, put it into a triangular flask filled with 90mL of sterile water, place it on a shaker at 150rpm for 30min, take it out, and dilute it step by step to 10 -1 , 10 -2 , 10 -3 , 10 -4 , 10 -5 , 10 -6 6 kinds of concentrations, the dilutions of 6 kinds of concentrations were spread on the screening medium, repeated 3 times, and cultured at 25°C ...

Embodiment 2

[0032] Example 2 Defense against Pseudomonas 13 degrading enzyme activity assay

[0033] The filter paper enzyme activity, endo-glucosidase activity, exo-glucosidase activity and β-glucosidase activity were determined by 3,5-dinitrosalicylic acid colorimetric method (DNS method).

[0034] 2.1 Preparation of glucose standard curve

[0035] Glucose standard solution: weigh 1g of anhydrous glucose dried at 103°C to constant weight, and dilute to 100mL with water;

[0036] Phosphate buffer: 0.1mol / L pH6.0 (suitable for neutral cellulase). Weigh 121.0 g of sodium dihydrogen phosphate monohydrate and 21.89 g of disodium hydrogen phosphate dihydrate, and dissolve them in 1 L of deionized water. Adjust the pH of the solution to 6.0;

[0037] DNS reagent: Weigh 10g of 3,5-dinitrosalicylic acid, put it in about 600mL of water, gradually add 10g of sodium hydroxide, stir and dissolve in a 50°C water bath (magnetic force), then add 200g of potassium sodium tartrate, After 2 g of phenol...

Embodiment 3

[0072] Embodiment 3 Defense Pseudomonas 13 bacteriostasis experiment

[0073] Fermentation enzyme production medium: CMC-Na10g, (NH 4 ) 2 SO 4 4.0g, MgSO 4 ·7H 2 O 0.5g, K 2 HPO 4 2g, beef extract 5g, peptone 10g (pH is naturally adjusted to 1L)

[0074] LB liquid medium: tryptone (Tryptone) 10g / L, yeast extract (Yeast-extract) 5g / L, sodium chloride (NaCl) 10g / L, adjusted to pH 7.0.

[0075] LB solid medium: tryptone (Tryptone) 10g / L, yeast extract (Yeast-extract) 5g / L, sodium chloride (NaCl) 10g / L, agar 20g / L adjusted to pH 7.0.

[0076] PDA medium: 6.0g potato flour, 20.0g glucose, 20.0g agar, pH 5.4-5.8

[0077] 3.1 Phomopsis

[0078] Phomopsis smeared on PDA plate, 37 ℃, after culturing for 7 days, wash the spores with physiological saline, Phomopsis is the suspension of Phomopsis spores.

[0079] Defense against Pseudomonas 13 bacteria solution was inoculated into a test tube containing 5 mL of fermented enzyme production medium according to the inoculum amoun...

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Abstract

The invention provides pseudomonas protegens inhibiting phomopsis. The pseudomonas protegens is pseudomonas protegens 13, and is preserved in the Chinese typical culture preservation center on December 5, 2018, wherein the preservation number is CCTCC NO: M 2018861. The pseudomonas protegens 13 has a good cellulose degradation ability, can produce cellulase, has stronger incision glucosidase activity, filter paper enzyme activity, excision enzyme activity and beta-glucosidase activity, and has application value in the production of the cellulase. The pseudomonas protegens 13 can inhibit the phomopsis. In addition, the pseudomonas protegens 13 can inhibit the growth of escherichia coli, staphylococcus aureus, candida albicans, shigella dysenteriae and enterobacter faecalis, and has development and utilization value in inhibiting human pathogenic bacteria. The invention also provides the application of the pseudomonas protegens 13 in producing cellulase and controlling kiwi soft rot.

Description

technical field [0001] The invention belongs to the technical field of microorganisms, and in particular relates to a defense against Pseudomonas inhibiting Phomopsis and its application. Background technique [0002] Phomopsis (Phomopsis) is a large genus in the fungus of Deuteromycota, Coelospora, Coccoides, and Coccoidaceae. It contains more than 100 different species and can parasitize more than 70 different families. plant. The pathogenic bacteria of this genus are widely distributed in regions, causing serious diseases such as leaf blight, branch blight, stem rot, ulcer and fruit rot of plants, resulting in significant economic losses. For example, it is the soft rot of kiwi fruit after picking. The pathogenic bacteria of kiwifruit branch blight, peach stiff buds, and plantain ear blight. [0003] At present, the prevention and control of Phomopsis mainly adopts chemical pesticides, such as: Yang Tingmi etc. adopt 8 kinds of pesticides to indoor toxicity and field c...

Claims

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Application Information

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IPC IPC(8): C12N1/20C12N9/42A01N63/02A01P3/00A01P1/00C12R1/38
CPCC12N9/2437C12Y302/01004C12R2001/38C12N1/205A01N63/10
Inventor 王金昌靳亮关丽梅郭燕
Owner INST OF MICROBIOLOGY JIANGXI ACADEMY OF SCI
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