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Metarhizium lepidiotae, microbial insecticide, preparation method and application

A microbial insecticide, Metarhizium anisopliae technology, applied in the field of preparation of microbial insecticides, Metarhizium anisopliae, can solve the problems of high toxicity of chemical pesticides and pesticide residues, and achieve resistance to pesticides, high lethality, The effect of promoting plant growth

Active Publication Date: 2021-04-13
MOON (GUANGZHOU) BIOTECH CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] At present, there are problems such as high toxicity of chemical pesticides, pesticide residues in crops, and resistance of pests

Method used

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  • Metarhizium lepidiotae, microbial insecticide, preparation method and application
  • Metarhizium lepidiotae, microbial insecticide, preparation method and application
  • Metarhizium lepidiotae, microbial insecticide, preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0050]In this embodiment, the squama is preserved, and the preservation name is the Matrodhiziumlepidiotae MN114915, the preservation number is, the preservation time is, the deposit address is, the classification name is.

[0051]The separation of the above strains, the purification method includes the steps of sequential:

[0052]Soil: After collecting the agricultural soil of Guangxi, after drying, remove the soil samples to remove impurities, weigh the dried soil 10G to load the filtration device.

[0053]Washing: Washing soil with tap water, soil particles flow by 1mm brass net and two polypropylene filters. The bottom of the soil particles were collected, put it in a sterile 50 ml centrifuge tube, add 50 ml of sterile water, and the scroll mixer is suspended. Then centrifuge at 10,000 rpm, poured down, washed with sterile water, centrifugally, and washed 3 times.

[0054]The precipitate was then diluted: a sterile carboxymethylcellulose solution solution was added to the proportion of wat...

Embodiment 2

[0058]The strains obtained by separated from Example 1 were separately analyzed and molecular biological identification.

[0059]Morphological identification:

[0060]The isolated squamous spaclasmia was inoculated at 28 ° C for 15 ° C on the SDAY medium plate at 28 ° C for 15 days. The white mycetes were collected into a production piece after 4 to 5 days, and the bacteria and the spore pendulum form were observed under the microscope; and the spores were collected from 10 to 12 days to prevent the size and morphology of the spore. Forms of colonies in the record colonies in 15 days.

[0061]figure 1 As shown in the vaccination 4 to 5 days, the microgram after the white mycelium production is picked, and the magnification is 400 times.figure 2 The microgram after the inoculation of the spore production is picked up after 10 to 12 days, and the magnification is 400 times.image 3 A front view of the colonies of the Mn113832 strain for 15 days,Figure 4 Rear view of the colony form of the Mn113...

experiment example 1

[0078]In this first experiment, the strain MN113832, MN114915 separated from Example 2 was respectively biological assays, and the effect of the temperature on the strain MN113832, MN114915, and was measured on the growth rate, spore, spore germination rate of colonies.

[0079](1) The effect of temperature on the growth of strains.

[0080]The cultured squamous spore spore was washed with 0.1% Tween 8, and 10 μl was taken into a new SDAY medium, respectively at 20 ° C, 25 ° C, 28 ° C, 30 ° C, respectively, five different temperatures at 37 ° C. Temperature culture, measure the diameter of colonies every day, and three repetitions are set each temperature treatment group.

[0081](2) Determination of colony growth rate.

[0082]The cultured squamous spore spore was washed with 0.1% Tween 80, and 10 μl was taken to the new SDAY medium, and three repetitions were determined, and the diameter was measured and data was recorded until the colonies were full of medium.

[0083](3) Determination of spore...

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Abstract

The invention discloses metarhizium lepidiotae, a microbial insecticide, a preparation method and application. The invention relates to the metarhizium lepidiotae strain, wherein the preservation name is Metarhizium lepidiotae MN114915, the preservation number is GDMCC61330, the preservation time is December 1, 2020, the preservation address is the Guangdong Microbial Culture Collection Center, the specific address is 5th floor, No.59 building, No.100 yard, Xianlie Middle Road, Guangzhou, and the classification name is Metarhizium lepidiotae. The new metarhizium lepidiotae is separated from soil by the inventor, has a high-toxicity insecticidal function, and is simple in culture method, rapid in growth and high in sporulation quantity. The metarhizium lepidiotae does not destroy the ecology, does not easily generate drug resistance, has high biological safety, and can be widely used in locust prevention and control.

Description

Technical field[0001]The present invention relates to the field of biological prevention and treatment, and in particular, there is a method and application method and application of microbial pesticide, preparation method.Background technique[0002]Metarhizium is a class of important insect fungi, more than 200 pests around the world can be killed by this fungal infection. The spores of the bacteric bacteria can be attached to pest epidermals, penetrating skin into pests, using pests and nutrient growth, and secrete toxins until pests have died. The body after the death of pests can release new spores, and infect other pests. In addition, Green bacteria is also common in the soil, which can be separated from the root soil and have a certain relationship with plant growth.[0003]At present, Green bacteria has about 30 species worldwide (Kepleer et al. 2014), and different green spacium species can infect death pests, and there is a certain difference in toxicity. Metarhizium Lepidiota...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N1/14A01N63/30A01P7/04A01P7/02C12R1/645
CPCA01N63/30Y02A50/30
Inventor 陈娟李远玉李书萌李东梅黄盼盼陈泽怡
Owner MOON (GUANGZHOU) BIOTECH CO LTD