A strain of Debaryoyces hansenii strain and its application
A technology of strains and yeasts, applied in applications, fungicides, fungi, etc.
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Embodiment 1
[0031] Embodiment 1 Debaryomyces hansenii of the present invention ( Debaryomyces hansenii ) Isolation and strain identification of XBL01
[0032] 1. Sample collection
[0033] Grapes are collected from organic orchards in northern China.
[0034] 2. Isolation and screening of strains and antagonistic screening
[0035]Isolate strains from organic grapes, use conventional gradient dilution coating to isolate, use PDA (containing streptomycin sulfate 25mg / L) and YPD agar (containing streptomycin sulfate 25mg / L) a total of two culture media at 25 ℃ respectively cultured under the same conditions, pick the colonies with large differences in colony morphology and can be purely cultivated, and purify and preserve them on YPD agar medium (containing streptomycin sulfate 25mg / L), and use postharvest Botrytis cinerea as the target pathogen to carry out antagonistic antibacterial treatment. The primary screening and multiple re-screening finally obtained a strain of Debaria hansenii...
Embodiment 2
[0042] Example 2 Low temperature tolerance test of Debaria hansenii XBL01 CGMCC No.10464 strain of the present invention
[0043] At present, Debaryomyces hansenii ( Debaryomyces hansenii ) The suitable growth temperature range is generally 20-30°C, and it can grow at 37°C. But the Debaryomyces hansenii described in this application ( Debaryomyces hansenii ) The suitable growth temperature of XBL01 CGMCC No.10464 strain is 15-28°C, but it does not grow at 37°C. Its suitable growth temperature determination experimental method is as follows:
[0044] Add an equal amount of Debaria hansenii ( Debaryomyces hansenii ) XBL01 CGMCC No.10464 strain (10 6 cells) bacteria were inoculated into conical flasks containing 1 liter of YPD liquid medium (containing streptomycin sulfate 25mg / L), and then incubated at 4°C, 10°C, 15°C, 20°C, 25°C, 28°C, and 30°C respectively. Shake flask culture (180-200rmp) at ℃ for 96h. Among them, each treatment was sampled once every 12 hours, and the...
Embodiment 3
[0045] Example 3 Debariae hansenii XBL01 CGMCC No.10464 strain antibacterial effect test of the present invention
[0046] Pathogens tested:
[0047] Botrytis cinerea (Botrytis cinerea) Botrytis cinerea Per. ex Fr).
[0048] Postharvest Botrytis cinerea was selected as the indicator fungus, and the plate confrontation culture method was adopted.
[0049] The specific operation is as follows: Debaria hansenii ( Debaryomyces hansenii ) XBL01 CGMCC No.10464 strain was cultured on PDA medium at 25°C for 48 hours. Cultivate the indicator fungus on a PDA plate at a constant temperature of 25°C for 3-4 days, and use a sterile stainless steel puncher with a diameter of 0.7cm from the edge of the colony to make agar sheets with bacteria; Inoculate it at the center of the PDA plate, and at the same time, use a sterile inoculation loop to streak Debaria hansenii ( Debaryomyces hansenii ) XBL01 CGMCC No.10464 strain, with the plate only inoculated with pathogenic bacteria as a contr...
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