Metschnikowia fructicola for preventing and controlling postharvest diseases of fruits and vegetables, and preparation method and using method of metschnikowia fructicola
A technology for drupe mechie yeast and post-harvest disease, applied in the field of drupe mecca yeast, can solve the problems of biocontrol effect only being verified on a few fruits, lack of bacteriostatic spectrum strains, etc., and achieve significant social and ecological benefits and traits Stable and good application prospects
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Embodiment 1
[0019] Example 1: Biological properties of Metschnikowia fructicola strain BY33
[0020] 1. Morphological features
[0021] (1) YPDA medium (1% yeast extract powder, 2% peptone, 2% glucose, 1.8% agar, sterilized at 121°C for 20 minutes) was cultured at 26°C for 48h, and the colonies were round and white with smooth and round edges. The cell shape is ellipsoidal.
[0022] (2) After culturing in YPDA liquid medium for 24 hours, no mold was formed, the bacterial solution was turbid, and there was precipitation. Microscopically, the yeast cells were oval and budded.
[0023] 2. Molecular biological identification
[0024] Use the universal forward primer NL-1 (5'-GCATATCAATAAGCGGAGGAAAAG-3') and reverse primer NL-4 (5'-GGTCCGTGTTTCAAGACGG-3') to perform PCR amplification of yeast 26S rDNA D1 / D2 region nucleic acid sequence, and the PCR product The sequencing results were entered into the website www.NCBI.nlm.nih.gov for BLAST, the homologous sequences were downloaded from the G...
Embodiment 2
[0026] Implementation Example 2 The Inhibitory Effect of Drupe Metchiella BY33 on Apple Penicillium, Botrytis Botrytis and Black Spot
[0027] 1. Experimental protocol
[0028] Take out Metschnissiae BY33 from the -80°C refrigerator, activate it with YPDA medium (10g of yeast extract powder, 20g of peptone, 20g of glucose, 18g of agar, 1000ml of deionized water, natural pH, sterilized at 121°C for 30min), and pick Single colonies were placed in YPD liquid medium, cultivated at 26°C and 200r / min for 24h, centrifuged at 4000rpm for 5min, discarded the supernatant, washed the collected bacteria with sterile water for 3 times, and counted on a hemocytometer to prepare The concentration is 1×10 8 Cells / mL of Metchione druposum BY33 bacterial suspension.
[0029]Activate Penicillium expansum, Botrytis cinerea or Alternaria tenuissima on PDA medium plate, culture at 26°C for 7-14 days, scrape appropriate amount of spores, wash with sterile water Prepared to a concentration of 5 x ...
Embodiment 3
[0039] Implementation example 3 Inhibitory effect of drupe metchi yeast BY33 on pear fruit blue mold and gray mold
[0040] 1. Experimental protocol
[0041] Take out Metschnissiae BY33 from the -80°C refrigerator, activate it with YPDA medium (10g of yeast extract powder, 20g of peptone, 20g of glucose, 18g of agar, 1000ml of deionized water, natural pH, sterilized at 121°C for 30min), and pick Single colonies were placed in YPD liquid medium, cultivated at 26°C and 200r / min for 24h, centrifuged at 4000rpm for 5min, discarded the supernatant, washed the collected bacteria with sterile water for 3 times, and counted on a hemocytometer to prepare The concentration is 1×10 8 Cells / mL of Metchione druposum BY33 bacterial suspension.
[0042] Activate Penicillium expansum or Botrytis cinerea on a PDA medium plate, culture at 26°C for 7-14 days, scrape appropriate amount of spores, and prepare a concentration of 5×10 with sterile water. 4 cells / mL of Penicillium or Botrytis cine...
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