Meyerozyma guilliermondii suspension for controlling postharvest diseases of cherry tomato fruits
A technology for cherry tomato and postharvest diseases, which is applied in the directions of yeast-containing food ingredients, microorganism-based methods, and applications, etc., can solve the serious harm to human health and environmental safety of chemical fungicides, affect the effect of disease control, and the resistance of pathogenic microorganisms. and other problems, to achieve the effect of reducing the incidence of Botrytis cinerea, cost-effective, and convenient cultivation.
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Embodiment 1
[0026] Embodiment 1, the screening of Pichia mongolica yeast:
[0027] Sea sand from the Sansha Islands in Hainan Province is selected;
[0028] The culture reagent is tiger red (Red Bengal) medium;
[0029] The cultivation and screening conditions are: weigh 10g of sea sand, add 100mL of sterile water, shake at 200r / min for 30min, draw the supernatant, and then dilute the supernatant gradient with sterile water for 10, 10 2 、10 3 、10 4 Draw 100 μL from each gradient and spread evenly on the tiger red medium plate, culture in the incubator at 28°C for 3 days, select and purify according to the colony shape, microscopic examination and PCR amplification 16s rDNA sequencing confirmed that it was yeast Afterwards, they were stored on slant planes of NYDA medium.
[0030] Finally, the strain J-SS-CX was screened out, identified as Meyerozyma guilliermondii by 16s rDNA, and its colony characteristics were as follows: round, milky white, with neat edges, smooth and wet surface. ...
Embodiment 2
[0035] Embodiment 2, the preparation method of Pichia mongolia suspension:
[0036]Pichia mongolica J-SS-CX (CGMCC NO.17240) was stored in NYDA medium at low temperature (4°C), and when activated, it was taken out and cultured in NYDA medium at 28°C for 48 hours, and then subcultured repeatedly After 2 times, use an inoculation loop to inoculate the activated Pichia monteritima into the NYDB medium, cultivate it at 200 rpm and 28°C for 24 hours, and then absorb 1 / 50 of the volume of the medium to contain 12% NaCl. In the NYDB medium (that is, bacterial solution: NYDB medium containing 12% NaCl = 1:50 volume ratio), subculture at 200rpm and 28°C for 24h, collect the culture solution, and store at 4000rpm and 4°C After centrifugation for 15 min, the cells collected by centrifugation were washed twice with sterile distilled water to remove the culture medium. Dilute and resuspend the yeast cells with sterile distilled water, use a hemocytometer to determine the concentration und...
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