Arthrinium bacterial strain and uses thereof
A technology of Arthrospora and bacterial strains, applied in the field of microorganisms, can solve the problems of incomplete molecular structure information and undetermined molecular configurations, etc.
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Embodiment 1
[0020] Embodiment 1, the isolation and cultivation of Arthrinium sp. bacterial strain:
[0021] In the laboratory, according to the following conditions and steps of isolation and cultivation, the Arthrophyllum strain of the present invention can be obtained:
[0022] 1), collect Polygonum Polygonum from Tianmu Mountain Nature Reserve in Zhejiang, my country, disinfect the collected Polygonum Polygonum with sodium hypochlorite at a concentration of 0.5% (w / v) for 10 minutes, then rinse with sterile water and place on sterile filter paper to absorb the water ;
[0023] 2) Next, use a sterile blade to remove the outer skin layer of Polygonum hydroponica, cut it into tissue pieces about 1 cm in size, and transfer the tissue pieces to each tissue containing 100 μg·ml -1 On 2% (w / v) water agar plate of ampicillin and streptomycin, culture at 24°C;
[0024] 3) After the hyphae grow out, the top of the mycelium is transplanted to the PDA solid medium for cultivation, and cultivated ...
Embodiment 2、2
[0025] Example 2. Separation, extraction and structural identification of 2,3β-dihydroxycritosporine:
[0026] 1), Arthrophyllum strain Ph1012 fermented culture, carry out following steps successively:
[0027] The Arthrospora strain Phl012 was activated and cultured on PDA medium at 26°C for 7 days, and the bacterial cake at the edge of the colony was cut with a puncher with a diameter of 5mm, and inoculated into a 500mL Erlenmeyer flask containing PDB culture medium, and each bottle was inoculated with 3 Bacteria cake, 26°C, 120r / min shaking culture for 15 days, the filtrate after removing the mycelium by suction filtration is the fermentation broth.
[0028] 2), extraction, recrystallization and structure identification:
[0029] Extract the fermentation liquid obtained in the above step 1) with ethyl acetate, and then recover the ethyl acetate under reduced pressure to obtain the extract; recrystallize the above extract with ethanol to obtain a red prismatic single crysta...
Embodiment 3、2
[0040] The toxicity determination of embodiment 3, 2,3β-dihydroxycridosporine:
[0041]Toxicity of 2,3β-dihydroxycitrasporine was determined by the toxicity test on Artemia salina. Artemia eggs were cultured and hatched at 28°C for 24 hours in artificial seawater with pH 8.5. Artificial seawater was mixed with a series of concentrations of ciprosporin solution in a ratio of 1:1 and added to the test tube, and each treatment was repeated three times. At the same time, distilled water and podophyllotoxin were used as blank control and positive control respectively. Add 30 normal Artemia in each test tube, observe and record the number of dead Artemia in each treatment after cultivating for 24hr, calculate the corrected mortality, adopt the dose logarithm-mortality probability value method to calculate and obtain the half-inhibitory concentration (LC 50 ). The details are shown in Table 4.
[0042] Table 4
[0043]
[0044] According to the content of the above-mentioned t...
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