A kind of centipede algae extract and its application in the preparation of marine fouling biological control agent
A biological control agent, marine fouling technology, applied in the direction of biocides, plant growth regulators, chemicals for biological control, etc., can solve problems such as obvious seasonal changes
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Embodiment 1
[0022] Preparation of centipede algae extract:
[0023] (1) Cut the centipede algae into small sections and put them in a jar, extract 3 times with 2 times the volume of absolute ethanol, combine the resulting ethanol extracts, and distill under reduced pressure to remove ethanol to obtain the crude extract extract;
[0024] (2) Chromatographic column for crude extract extract (Xinweier ) separation, using eluent ethyl acetate / petroleum ether to carry out gradient elution at a volume ratio of 0 to 10:10 to 0, to obtain 20 components;
[0025] (3) contrast by thin-layer chromatography spot plate (developing agent CH 2 Cl 2 / MeOH=10 / 3, volume ratio, RF value 0.45), combined components 15-18 (ethyl acetate / petroleum ether obtained by volume ratio 40:60, 50:50, 60:40, 70:30 elution Components), and then use Sephadex LH-20 chromatographic column with MeOH / CH 2 Cl 2 The elution is carried out according to the volume ratio of 1:1, part of the pigment is removed, the eluate is c...
Embodiment 2
[0027] Experimental group: the centipede algae extract (prepared in Example 1) was dissolved in methanol solvent to prepare a solution with a concentration of 282.6 μg / mL. Add 1 mL of this solution to a petri dish with a diameter of 6 cm, and make it evenly cover the bottom of the petri dish. After the solvent is completely evaporated, the dose of centipede algae extract coated on the bottom of the petri dish is 10 μg / cm 2 . Add 13 mL of sea water.
[0028] Control group: Add 1mL of methanol solvent to make it evenly distributed on the bottom of the petri dish, and then add 13mL of seawater after the volatilization is complete.
[0029] Blank group: add 13mL seawater.
[0030] Four parallel samples were set up in each of the experimental group, the blank group and the control group. Add 30 netted barnacle Venus larvae to each sample. Place in a constant temperature incubator at a temperature of about 30°C and cultivate in a dark environment. Statistical analysis was perf...
Embodiment 3
[0035] Experimental group: the centipede algae extract (prepared in Example 1) was dissolved in methanol solvent to prepare a solution with a concentration of 282.6 μg / mL. Add 1 mL of the solution to a petri dish with a diameter of 6 cm and make it evenly cover the bottom of the petri dish. After the solvent is completely evaporated, the dose of centipede algae extract coated on the bottom of the petri dish is 10 μg / cm 2 . Add 13 mL of sea water.
[0036] Control group: add 1mL of methanol solvent, so that the solvent is evenly distributed on the bottom of the petri dish, and then add 13mL of seawater after the solvent is completely evaporated.
[0037] Blank group: add 13mL seawater.
[0038] Four parallel samples were set up in the experimental group, the blank group and the control group, and about 30 vegetal disc larvae were added to each sample. Cultivate in a dark environment in an incubator at a temperature of about 26°C. Statistical analysis was performed on the a...
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