Fresh keeping agent for blueberries as well as preparation method and application of fresh keeping agent
A preservative, blueberry technology, applied in application, fruit and vegetable preservation, food preservation, etc., to achieve high-quality preservation, integrity, and safe use.
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Embodiment 1 5
[0031] The inhibition of embodiment 1 Chinese gallnut extract, chitosan, ascorbic acid to Botrytis cinerea
[0032] 1. Preparation of Galla galla extract
[0033] Take high-quality dried Chinese gallnuts to remove internal worm eggs, then pulverize them completely with a high-speed pulverizer, use 75% (V / V) ethanol, material-to-liquid ratio 1:15 (W / V) ultrasonic extraction at room temperature (power 300W) for 1 hour, and centrifuge for 10 minutes. The supernatant was evaporated to dryness at 50° C., the obtained crude extract was redissolved in water, extracted with ethyl acetate, and the ethyl acetate layer was evaporated to dryness to obtain Galla galla extract.
[0034] 2. Inhibition test of gallnut extract, chitosan and ascorbic acid on botrytis cinerea
[0035] Tested strains and reagents: Botrytis cinerea was isolated from picked blueberries in our laboratory, and chitosan and ascorbic acid were purchased commercially.
[0036] Culture medium and culture conditions: ...
Embodiment 2
[0042] The bacteriostasis effect of embodiment 2 different concentrations Galla gall extract
[0043] Gallnut extract is dissolved in 10% Tween80 and fully emulsified. Cool the melted PDA medium to about 50°C, add a certain volume of Galla gall suspension, vortex and mix well, then pour the plate, so that the final concentration of the plate is 37.5 μL / mL, 75 μL / mL, 150 μL / mL, 300 μL / mL, and 600 μL / mL. The culture medium plate without Galla gall extract was used as a control. Use a sterile puncher to punch out a 6 mm diameter bacterial block on the pathogenic bacteria plate that has been cultivated for 7 days and place it in the center of the PDA plate (90 mm in diameter). Place it in a biochemical incubator at 28°C for 6 days, and observe the antibacterial effect. The colony diameter was measured by the cross method and the inhibition rate was calculated. There were 3 plates for each concentration gradient, and the experiment was repeated 3 times. Inhibition rate (%)=(...
Embodiment 3
[0044] Example 3 The influence of pH on the bacteriostatic effect of Galla gall extract
[0045] Acetic acid was used to adjust the pH value of gallnut extract to 2, 4, 6, 8, 10, 12, and the inhibitory effects of gallnut extracts with different pHs on Botrytis cinerea were compared respectively. The experimental process was as described in Example 1.
[0046] From figure 2 It can be seen that the pH has a greater influence on the antibacterial activity of the gallnut extract. As the pH value gradually increases, the diameter of the antibacterial zone of the gallnut extract gradually decreases, and the antibacterial activity of the gallnut extract is stronger under acidic conditions. However, under alkaline conditions, the antibacterial activity of gallnut extract was basically lost. This is because certain compounds containing carboxyl groups and phenolic hydroxyl groups in Galla gall extracts will dissociate to varying degrees as the pH value of the external environment i...
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