Brown alga polyphenol composition with alga inhibitory activity, and preparation method and application thereof
A technology of brown algae polyphenols and compositions, which is applied in the field of brown algae polyphenols compositions and its preparation, can solve the problems that there is no in-depth discussion on the growth inhibition of microalgae, no detailed research on active substances, and the extraction method needs to be optimized. Good extraction efficiency, reduced energy consumption, and improved output value
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Embodiment 1
[0037] Example 1. Preparation of Ascophyllum nodosum extracting brown algae polyphenol composition
[0038] Ascophyllum nodosum dry powder (100 mesh) was purchased from Stawest Botanicals, Canada.
[0039] The algae powder was extracted ultrasonically with 100mL of solvent, using an ultrasonic cell pulverizer (Ningbo Xinzhi), while assisting magnetic stirring, with a rotation speed of about 1,000rpm, a temperature controlled below 30°C, and 70% acetone as a solvent for extraction. After extraction, centrifuge at 10,000 rpm and 4°C for 10 minutes, take the supernatant and distill it under reduced pressure, freeze-dry it in a lyophilizer, and finally resuspend the extract in 20 mL of deionized water for use.
[0040] Table 1 Experimental results of Ascophyllum nodosum extraction conditions
[0041]
[0042] *The power is the percentage of the total power (950w) of the cell grinder
[0043] In addition, 50% and 75% acetone aqueous solution was also used as the extraction sol...
Embodiment 2
[0044] Example 2. Inhibition of the growth of "bloom" microalgae by the composition of brown algae polyphenols extracted from Ascophyllum nodosum
[0045] 2.1 Effect of Ascophyllum nodosum extract on the growth of microalgae
[0046] Two kinds of microalgae, Chlorella vulgaris and Scenedesmus sp., were respectively cultured in Erlenmeyer flasks filled with 30 mL of sterile culture solution. Except for the control, 1 mL of the Ascophyllum nodosum extract from Experiment d of Example 1 was added to each. After being cultured in a light incubator for 7 days, samples were taken to measure the cell density with a Countstar automatic cell counter (Inno-Alliance Biotech, Inc., USA) for calculating the inhibition rate. Calculated as follows:
[0047]
[0048] The two kinds of microalgae were respectively cultured in 100 mL of culture solution, and the amount of the extract added was such that its concentration in the culture solution was 3% (volume ratio). The culture conditions ...
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