Method for efficiently extracting gutta-percha
A high-efficiency technology of eucommia gum, which is applied in the direction of isolating microorganisms and adding compounds to stimulate growth, etc., can solve the problems of not mastering the optimal culture conditions of eucommia gum strains, not being able to exert the best performance of the strains, and not being able to fully measure the strains, etc. Achieve convenient screening and confirmation, improve assay efficiency, and increase amplification multiples
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Embodiment 1
[0032] refer to figure 1 , a method for efficiently extracting eucommia gum, comprising the following steps:
[0033] S1: Soil sampling, collecting the humus soil under the eucommia forest, and then set aside;
[0034] S2: Enrichment culture, adding the soil from Eucommia ulmoides forest to the culture medium to enrich bacteria, thermophiles and fungi. By enriching the soil, more colonies can be obtained, which is convenient for later culture experiments;
[0035] S3: Separation by coating. After the enrichment, take 100 μL of the bacterial liquid and use the plate coating method to separate the bacteria. Pick the strains with fast growth rate, dominant colony number, different color and shape, and carry out the isolation, purification and preservation of the strains. Separation of bacteria by coating method, and then picking the bacteria with fast growth rate and dominant number of colonies for inoculation can quickly separate the colonies, which is convenient for subsequent...
Embodiment 2
[0044] refer to figure 1 , a method for efficiently extracting eucommia gum, comprising the following steps:
[0045] S1: Soil sampling, collecting the humus soil under the eucommia forest, and then set aside;
[0046] S2: Enrichment culture, adding the soil from Eucommia ulmoides forest to the culture medium to enrich bacteria, thermophiles and fungi. By enriching the soil, more colonies can be obtained, which is convenient for later culture experiments;
[0047] S3: Separation by coating. After the enrichment, take 100 μL of the bacterial liquid and use the plate coating method to separate the bacteria. Pick the strains with fast growth rate, dominant colony number, different color and shape, and carry out the isolation, purification and preservation of the strains. Separation of bacteria by coating method, and then picking the bacteria with fast growth rate and dominant number of colonies for inoculation can quickly separate the colonies, which is convenient for subsequent...
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