Fruit disease control method based on saccharomyces cerevisiae cell wall product induction activity resistance
A technology of Saccharomyces cerevisiae cells and inducing resistance, which is applied in the preservation of food ingredients as antimicrobials, food science, preservation of fruits and vegetables, etc. Low cost, high cost performance, good social and ecological benefits
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Embodiment 1-1
[0042] Embodiment 1-1, the preparation that suppresses fruit postharvest disease by inducing resistance,
[0043] Saccharomyces cerevisiae with the preservation number CGMCC No.2.3854 was stored at low temperature (4°C) in NYDA medium (beef extract 8g, yeast extract powder 5g, glucose 10g, agar 20g, water to 1000mL, at 0.1MPa, 121 Under high pressure steam sterilization at ℃ for 20min), take out after activation, culture in NYDA medium at 25℃ for 48h, repeat subculture twice, use the inoculation loop to inoculate the activated yeast into NYDB, at 200rpm, After culturing at 28° C. for 24 hours, the culture medium was collected, centrifuged at 3000 g for 10 min, washed with sterile distilled water three times to remove residual culture medium, and the precipitate was collected by centrifugation to obtain Saccharomyces cerevisiae cells.
[0044] Saccharomyces cerevisiae was resuspended in 0.2mol / L phosphate buffer (PBS, pH 8.0) to prepare 1×10 8 cell / mL bacterial suspension. Ad...
Embodiment 2-1
[0047] Embodiment 2-1, the preparation that suppresses fruit postharvest disease by inducing resistance:
[0048] Saccharomyces cerevisiae with the preservation number CGMCC No.2.3854 was stored at low temperature (4°C) in NYDA medium (beef extract 8g, yeast extract powder 5g, glucose 10g, agar 20g, water to 1000mL, at 0.1MPa, 121 Under the condition of high pressure steam sterilization for 20min at ℃), take it out during activation, and culture it in NYDA medium at 25℃ for 48h. After culturing at 28° C. for 24 hours, the culture medium was collected, centrifuged at 3000 g for 10 min, washed with sterile distilled water three times to remove residual culture medium, and the precipitate was collected by centrifugation to obtain Saccharomyces cerevisiae cells.
[0049] Saccharomyces cerevisiae was resuspended in 0.2mol / L phosphate buffer (PBS, pH 8.0) to prepare 1×10 8 cell / mL bacterial suspension. Add 0.5 g of acid-washed glass beads (Sigma, particle size 425-600 μm) to 0.5 m...
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