Serratia grimesii and application thereof
A technology of Serratia gasseri and bacterial agent, applied in the field of microorganisms, can solve the problems of environmental pollution, decreased control effect, endangering the health of humans and animals, etc.
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[0066] The preparation method of potato liquid medium is as follows: take 200 g of peeled potatoes, cut them into small pieces, add 1.0 L of distilled water, and boil for 30 minutes; collect the filtrate after gauze filtration, add 20.0 g of glucose to the filtrate, and distill the volume to 1.0 L, and then sterilized at 115°C for 15 minutes. There is no need to adjust the pH value of the potato liquid medium, that is, the pH value is natural.
[0067] The preparation method of potato liquid medium 1 is as follows: take 200 g of peeled potatoes, cut into small pieces, add 1.0 L of distilled water, and boil for 30 minutes; collect the filtrate after gauze filtration, add 20.0 g of glucose in the filtrate, and distill to volume with distilled water to 1.0L, adjust the pH to 4.0; then sterilize at 115°C for 15 minutes.
[0068] Potato liquid medium 2: In the preparation method of potato liquid medium 1, "adjust the pH value to 4.0" was replaced with "adjust the pH value to 5.0",...
Embodiment 1
[0074] Example 1. Isolation, identification and preservation of Serratia grimesii (Serratia grimesii) S-2CGMCC No.13034
[0075] 1. Separation
[0076] 1. Processing of soil samples
[0077] (1) Add 10 g of soil sample (collected from the potato soil in Guyuan County, Ningxia Hui Autonomous Region) and an appropriate amount of glass beads to 90 mL of sterile water, vibrate for 10 min, and let stand for 30 s to make a soil stock solution (at this time, the dilution is recorded as 10 -1 ). Take 1 mL of the supernatant of the soil stock solution and add it to a test tube filled with 9 mL of sterile water and mix well (the dilution is 10 at this time). -2 ), then draw 1mL from this test tube and add it to another test tube filled with 9mL sterile water and mix well, and so on to make dilution A (dilution is 10 -3 ) and diluent B (dilution of 10 -4 ).
[0078] 2. Take Streptomyces scab 4.76, inoculate it on an oat solid plate, and culture it statically at 28° C. for 10 days; t...
Embodiment 2
[0092] The propagation of embodiment 2, Serratia grisneri S-2
[0093] The specific steps for the propagation of Serratia gaseri S-2 are as follows:
[0094] 1. Activate Serratia gordonii S-2 on beef juice solid medium for three times, then pick a single colony and inoculate it in a 250mL Erlenmeyer flask containing 50mL beef juice liquid medium, 30°C, 200r / min Cultivate on a constant temperature shaker for 2 days to obtain a culture solution.
[0095] 2. After completing step 1, take the culture solution, centrifuge at 12000r / min for 1min, discard the supernatant, and collect the precipitate.
[0096] 3. After completing step 2, take the precipitate and resuspend it with 50 mL of sterile water to obtain a bacterial suspension (the concentration of Serratia grisneri S-2 is about 1.0×10 10 cfu / mL).
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