A kind of isocoumarin compound and its preparation method and application as natural marine biological antifouling agent
An isocoumarin and compound technology, which is applied in biochemical equipment and methods, biocides, microorganism-based methods, etc., can solve problems such as damage to the marine environment, immune system damage, poisoning, etc., and achieve a promising effect.
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Embodiment 1
[0016] (1) Culture of marine fungus Eurotium sp. (HM991283)
[0017] The medium used for the culture of the fungus Eurotium sp. (HM991283) contains 1.0% glucose (percentage by weight, the same below), 0.1% yeast extract, 0.2% peptone, 1.0% agar, 3% coarse sea salt, and the rest is water. When making a test tube slant, the fungal strains were cultured at 28°C for 5 days.
[0018] (2) Fermentation of marine fungus Eurotium sp. (HM991283)
[0019] The fermentation medium used for the fermentation culture of the fungus Eurotium sp. (HM991283) contains glucose 1.0% (percentage by weight, the same below), yeast extract 0.1%, peptone 0.2%, coarse sea salt 3.0%, and the rest is water. Cultivate for 30 days.
[0020] (3) separation and extraction of formula I compound of the present invention
[0021] Get 100L of fermented product of step (2) gained, after fermented liquid and thalline are separated, fermented liquid is extracted 5 times with ethyl acetate, extract is concentrated u...
Embodiment 2
[0030] (1) Culture of marine fungus Eurotium sp. (HM991283)
[0031]The strain medium contains glucose 0.1%-5.0% (weight percentage, the same below), yeast extract 0.01%-2%, peptone 0.01%-2%, agar 0.1%-3.0%, coarse sea salt 0.05%-5%, and the rest It is water; the cultivation temperature is 5-45° C.; the cultivation time is 3-10 days.
[0032] (2) Fermentation of marine fungus Eurotium sp. (HM991283)
[0033] The fermentation medium contains 0.1%-5.0% of glucose (percentage by weight, the same below), 0.01%-2% of yeast extract, 0.01%-2% of peptone, 0.05%-5% of coarse sea salt, and the rest is water; the culture temperature is 5- 45°C; culture time is 5-50 days.
[0034] (3) separation and extraction of formula I compound of the present invention
[0035] Get 50L of the fermented product obtained in step (2), separate the fermented liquid from the thalline, extract the fermented liquid 2 to 6 times with ethyl acetate, concentrate the extract under reduced pressure to obtain t...
Embodiment 3
[0038] The marine fungus Eurotium sp. (HM991283) was cultured in the strain medium, and then the above-mentioned marine fungus was fermented and cultured in the fermentation medium. After the fermentation liquid and the bacteria were separated, the fermentation liquid was extracted with ethyl acetate , the extract was concentrated under reduced pressure to obtain a fermented liquid extract; the cells were extracted with methanol and concentrated under reduced pressure to obtain a cell extract; (Compound 1-12) is the compound of formula I, and its structure confirmation data is consistent with the corresponding data in Example 1. Wherein the strain medium contains glucose, yeast extract, peptone, agar, coarse sea salt, water, and the fermentation medium contains glucose, yeast extract, peptone, coarse sea salt, water; the chromatographic separation is normal phase Silica gel column chromatography and high performance liquid chiral chromatography.
[0039] In order to explore a...
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