A kind of trichothecene compound and its preparation method and application
A technology for trichothecenes and compounds, which are applied in the field of trichothecenes and their preparations, and can solve problems such as unseen drugs and the like
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Embodiment 1
[0021]A trichothecenes compound, the structural formula is as shown in Ι:
[0022](Ι).
Embodiment 2
[0024]The preparation method of trichothecenes as shown in the formula I in Example 1, specifically includes the following steps:
[0025](1) Fermentation production
[0026]The Fusarium with the deposit number CGMCC No. 14121 (Fusarium sp.) Bacteria were resurrected by streaking, inoculated into PDB solid medium, and activated in a 28℃ incubator for 3 days. Use an inoculating needle to pick a colony from the slope and inoculate it into the PDB liquid medium. Shake culture on a shaker at 180 rpm for 3 days to obtain a seed solution. Then, the seed solution was inoculated into the PDB liquid medium at a volume ratio of 10%, and cultured at 28°C on a shaker at 180 rpm for 12 days to obtain a strain Fermented product, strain fermented product is filtered through gauze to obtain mycelium and fermentation broth;
[0027](2) Obtaining extract
[0028]The mycelium obtained in step (1) was added to methanol to be ultrasonically broken, and then extracted three times with equal volume of ethyl acetate....
Embodiment 3
[0037]In vitro antibacterial activity test (96-well plate antibacterial test)
[0038](1) Experimental samples
[0039]Preparation of the test sample solution: The test sample is the pure compound separated and purified in the above-mentioned Example 1. An appropriate amount of the sample is accurately weighed, and a solution of the required concentration is prepared with methanol to test the activity. The indicator bacteria used in this experiment is the common aquatic pathogen Vibrio harveyi.
[0040](2) Experimental method
[0041]96-well plate antibacterial test method: After preparing the medium, sterilize it for about two hours, dry and cool it to activate the bacteria. Vibrio harveyi was inoculated into LB solid medium and cultured at 37°C for 24 hours. The bacteria in the LB solid medium were inoculated into the LB liquid medium and cultured at 37°C for 12 hours. The cell suspension was added to a 96-well plate, and each gradient of the compound to be tested was added. The solvent used ...
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