Paecilomyces lilacinus space mutation mutant strain Sd-m-16 and microbial preparation and application thereof
A technology of Paecilomyces lilacinus and microbial preparations, applied in the field of Paecilomyces lilacinus
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Embodiment 1
[0029] Example 1 Preparation of Paecilomyces lilacinus wettable powder
[0030] 1. Preparation of Sd-m-16 spore powder of Paecilomyces lilacinus (P.lilacinus) aerospace mutation mutant strain
[0031] (1), preparation of Paecilomyces lilacinus fermentation broth
[0032] 1. After activating the Paecilomyces lilacinus space mutation mutant strain Sd-m-16, carry out shake flask seed culture;
[0033] The composition of shake flask seed culture medium (by mass percentage):
[0034] Glucose 1.5-2%
[0035] Sodium nitrate 0.4-0.6%
[0036] Ammonium sulfate 0.2-0.3%
[0037] Soy flour 0.2-0.3%
[0038] Dipotassium hydrogen phosphate 0.1-0.2%
[0039] Magnesium sulfate 0.1-0.2%
[0040] water balance
[0041] Liquid fermentation conditions: put 200ml of seed medium into a 500ml triangular flask, inoculate Paecilomyces lilacinus spore suspension after autoclaving, the inoculation amount is 1.5-3%, place at 24-28°C, shaker 150-200r / min, cultivated for 18-36h.
[0042] 2. Sec...
experiment example 1
[0071] Experimental example 1 Screening of Paecilomyces lilacinus 20-7 space-flight mutagen and determination of mutagenic effect
[0072] 1 Experimental materials and methods
[0073] 1.1 Strains
[0074] For the test Paecilomyces lilacinus (P.lilacinus) 20-7, Shandong (Sd) strains. After spaceflight mutagenesis and returning to the ground, it is stored in the laboratory at 4°C for future use.
[0075] 1.2 Aerospace carrying
[0076] Paecilomyces lilacinus 20-7 and Shandong (Sd) strains were divided into two parts respectively, one part was left on the ground for routine storage as a control (CK); the other part was carried on "Shenzhou" 8 spaceship, which lasted 6d20h. After returning to the ground, take out the materials in time and store them at low temperature.
[0077] 1.3 Mutant Screening
[0078] The Paecilomyces lilacinus strain and the wild-type strain (CK) treated by aerospace mutagenesis were respectively made into spore suspensions and diluted to 10 3 times...
experiment example 2
[0122]Experimental example 2 Determination of the pathogenicity of Paecilomyces lilacinus 20-7 spaceflight mutagen to root-knot nematode eggs
[0123] 1. Experimental method
[0124] Prepare 10 with sterile water 3 / mL root-knot nematode egg suspension, add 0.5mL of the egg suspension, 50μL spore liquid, and 4.5mL sterile water to a 6cm small Petri dish. A small petri dish without spore solution was used as a control. Each mutant strain was repeated 3 times, that is, 3 dishes for each. Incubate at 25°C for 4 days. Microscopic examination, 50 eggs were randomly counted in each dish, the number of parasitized eggs was counted, and the egg parasitism rate of each bacterial strain was calculated. Egg parasitism rate (%) = (average number of parasitized eggs in 3 repeated tests of this strain / 50) × 100%.
[0125] 2. Experimental results
[0126] It has been observed that root-knot nematode eggs can be infected 2 days after inoculation, and most of the parasitized eggs are egg...
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