A strain of Pantoea agglomerans and its application
A technology of Pantoea agglomerans and bacterial agents, applied in the field of microorganisms, can solve the problems of little effect and achieve good effect and low cost
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example 1
[0020] Step 1: The ZLSY16 strain that has been screened and purified is preferred, sterilized with standard solid LB medium, added 1% volume of Eupatoria adenophorum extract before solidification, and adjusted the pH value to 7.0, poured plate, After cooling, inoculate ZLSY16 on the culture medium, culture at 28°C for 24 hours, and divide the solid culture medium with bacteria into 1cm 2 A small piece of spare. Step 2: Configure standard liquid LB medium, add 1% Eupatorium adenophorum extract according to the volume ratio after sterilization, adjust the pH value to 7.0, cool down to 35°C, and prepare 1cm of bacteria-carrying medium in the previous step 2 The small pieces of culture medium were inoculated (added) into the liquid medium in proportion, cultured at 28°C for 24 hours, then taken out and cooled to 8°C for 6 hours. Step 3: Take out the refrigerated bacteria-carrying liquid medium, dilute it according to the volume ratio medium: water ratio of 1:10, and spray it on t...
example 2
[0022] Step 1: The screened and purified ZLSY16 strain is preferred, sterilized with standard solid LB medium, add 1% Eupatoria adenophorum extract before solidification, and adjust the pH value to 7.0. Pour the plate and wait for condensation Then ZLSY16 was inoculated onto the medium, and after culturing on the medium at 32°C for 24 hours, the culture medium with bacteria was divided into 1cm 2 A small piece of spare. Step 2: Configure standard liquid LB medium, add 1% Eupatorium adenophorum extract according to the volume ratio after sterilization, adjust the pH value to 7.0, cool down to 35°C, and prepare 1cm of bacteria-carrying medium in the previous step 2 Small pieces of culture medium were inoculated (added) into the liquid culture medium in proportion, cultured at 32°C for 24 hours, then taken out and cooled to 8°C for 6 hours. Step 3: Take out the refrigerated bacteria-carrying liquid medium, dilute it according to the volume ratio medium: water ratio of 1:10, and ...
example 3
[0024] Step 1: The screened and purified ZLSY16 strain is preferred, sterilized with standard solid LB medium, add 1% Eupatoria adenophorum extract before solidification, and adjust the pH value to 7.0. Pour the plate and wait for condensation Then ZLSY16 was inoculated onto the culture medium, and after culturing on the culture medium at 28°C for 24 hours, the bacteria-carrying medium was divided into 1cm 2 A small piece of spare. Step 2: Configure standard liquid LB medium, add 1% Eupatorium adenophorum extract according to the volume ratio after sterilization, adjust the pH value to 7.0, cool down to 35°C, and prepare 1cm of bacteria-carrying medium in the previous step 2 The small pieces of culture medium were inoculated (added) into the liquid medium in proportion, cultured at 28°C for 24 hours, then taken out and cooled to 8°C for 6 hours. Step 3: Take out the refrigerated bacteria-carrying liquid medium, dilute it according to the volume ratio medium: water ratio of 1:...
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