Application of a quinazolinone alkaloid compound derived from marine fungi in marine fouling biocontrol
A technology of quinazolinone and marine fungus, which is applied in the field of application of quinazolinone alkaloid compounds in marine fouling biological control, achieving good social benefits, reliable and stable sources, and great potential for popularization and application
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Embodiment 1
[0028] The quinazolinone alkaloid compound of the present invention can be isolated from the cell of the marine fungus Aspergillus sp. SK-28. The marine fungus was isolated from the leaves of the mangrove plant Candela in the Shankou Mangrove Reserve of Guangxi Zhuang Autonomous Region; the specific steps are as follows:
[0029] 1. Seed culture:
[0030] 1.1 Preparation of seed medium: 200g of potatoes, 20g of glucose, 1L of tap water, equally distributed in five 500mL Erlenmeyer flasks, and extinguished at 121°C for 30 minutes.
[0031] 1.2 Cultivation of seeds: Inoculate the strains of marine fungi into the seed medium, place them on a shaker at a speed of 200 rpm at a temperature of 28° C., and cultivate them for 72 hours to obtain a seed culture solution.
[0032] 2. Fermentation culture:
[0033] 2.1 Prepare fermentation medium: 6000g rice, 180g sea salt, 6L tap water, extinguish at 121°C for 30 minutes.
[0034] 2.2 Fermentation culture: Aseptically transfer 5 mL of ...
Embodiment 2
[0038] Anti-biofouling activity experiment is carried out to the quinazolinone alkaloid compound in embodiment 1:
[0039] In the experimental group, the quinazolinone alkaloid compound was dissolved in methanol 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 content of the quinazolinone alkaloid compound coated on the bottom of the petri dish is 10 μg / cm 2 .
[0040]Add 1mL of methanol to the control group, so that the solution is evenly distributed on the bottom of the petri dish, and then add 10mL of seawater after the solvent is completely evaporated.
[0041] Only 10 mL of seawater was added to the blank group.
[0042] Three parallel samples were set up for each of the experimental group, the control group and the blank group. Add 30 netted barnacle Venus larvae to each sample. Place them...
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