A kind of compound bacterial strain based on hydrogen oxidizing bacteria and culture method thereof
A technology of compound strains and culture methods, applied in the field of microorganisms, can solve the problems of low strain abundance ratio and unfavorable industrial application, etc.
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Embodiment 5
[0064] This embodiment provides a method for preparing a synthetic medium of the present invention, the specific steps are as follows:
[0065] (1) The organic compound is configured into a mixed solution according to the ratio of Example 1, stirred and dispersed evenly.
[0066] (2) Minerals are configured according to the ratio of Example 1, added to the mixed solution of organic compounds, stirred and dispersed evenly, and the minerals form a suspended dispersion state in the mixed solution of organic compounds, and the turbidity is relatively high and opaque by visual inspection.
[0067] (3) adding pure water to dilute to make the total weight 100kg, continue to stir and disperse, and obtain a liquid synthetic medium after dilution.
[0068] (4) The liquid synthetic culture medium is sterilized in a cycle through an ultraviolet light device, and the sterilization time is more than 30 minutes. Put the sterilized medium into the culture container.
[0069] The medium prep...
Embodiment 6
[0073] The cultivation method of embodiment 6 composite strains
[0074] Step 1: Take peat soil with a humidity of 16% from under the vegetation in the original ecological environment of the Dinghushan National Nature Reserve in Guangdong, China, dissolve it in water, stir and dilute it, and then precipitate it, and take 1L of the supernatant as the primary strain;
[0075] Step 2: Inoculate the primary strains into the liquid medium of Example 1 for cultivation, feed compressed air, and the volume ratio relationship between liquid and air flow is 1m 3 :5-15m 3 / h, preferably, the air flow is 0.8-1m 3 / h, the temperature is controlled at 28-32°C, preferably 30-32°C. Stop the air supply after 7 days of enrichment culture, let it stand for 24 hours to settle, and separate the supernatant after the minerals precipitate to the bottom of the container to obtain the secondary strain.
[0076] Step 3: Put the secondary strains into the same reaction container; feed compressed air ...
Embodiment 7
[0087] This example adopts the cultivation method of the compound strain of Example 6, and this example uses the culture medium prepared in Example 2. The only difference between this example and Example 6 is that step 1 of this example is obtained from Mangshan, Hunan, China National Level Under the vegetation in the original ecological environment of the nature reserve, peat soil with a humidity of 30% was taken, dissolved in water, stirred and diluted, and then precipitated. Take 1L of the supernatant as the primary strain.
[0088] In this embodiment, samples were taken and tested at the culture time points of 0h, 24h, 36h, 72h, 96h, 7 days, 14 days, and 21 days, and the test results are shown in Table 6.
[0089] Table 6: Detection results at different time points during the cultivation process of Example 7
[0090]
[0091] Remarks: ①Represents Hydrogenophaga laconesensis HWB-10 T②Represents Pseudomonas wadenswilerensis CCOS 864T ③Represents Azospirillum rugosumIMMIB...
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