Atlantibacter hermannii for degrading methyl mercury and application thereof
A technology of methylmercury and bacilli, applied in the field of microorganisms, can solve problems such as limited understanding of biodegradation
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Embodiment 1
[0014] Example 1. Screening and identification of strains
[0015] The applicant, Huazhong Agricultural University, obtained a strain of unknown classification and function from the China Agricultural Microorganism Culture Collection Management Center, recovered and expanded the culture, and sent it to Shanghai Meiji Biomedical Technology Co., Ltd. for whole genome extraction and sequencing of amplified products . The obtained gene sequences were homologously compared by GeneBank to determine their taxonomic status.
[0016] The result shows that its gene sequence is 99% similar to the 16S rRNA gene sequence of Atlantibacter hermannii. The bacterial strain belongs to Atlantibacter hermannii. The sequencing result is shown in SEQ ID No.1.
[0017] The applicant classified and named the strain Atlantibacter hermannii L-1, and sent it to the Chinese Type Culture Collection Center (CCTCC) of Wuhan University, Wuhan City, Hubei Province on October 26, 2021 for preservation. The n...
Embodiment 2
[0018] Functional verification of the strain of Example 2
[0019] 1. Recovery and expansion of strains
[0020] (1) Open the ampoule tube of freeze-dried bacteria in an aseptic operation, add an appropriate amount (0.3ml) of YM agar liquid medium to the freeze-dried powder of the bacteria with a sterile pipette, and shake gently to dissolve the freeze-dried bacteria into a Suspended. Aspirate all the bacterial suspensions, transplant them into slant culture medium (no more than 2 tubes), and culture them statically at 28°C. This is the first-generation culture;
[0021] (2) Take the first-generation culture with an inoculation loop, inoculate it in YM liquid medium, and shake it in a shaker at 28°C for 24 hours, which is the second-generation culture, and cultivate it to the required number of generations in this way.
[0022] 2. Functional verification of strains
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