Saccharomyces ellipsoideus for preventing and treating postharvest diseases of fruits and vegetables and preparation and use methods thereof
A technology for Saccharomyces cerevisiae and post-harvest diseases, applied in the field of Saccharomyces cerevisiae, can solve the problems that the biocontrol effect is only verified on a small number of fruits, and the lack of antibacterial spectrum strains, etc., achieves significant social and ecological benefits, stable properties, and safety sex high effect
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Embodiment 1
[0019] Example 1: Biological properties of the wine Saccharomyces ellipsoideus strain BY36
[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...
Embodiment 2
[0026] The inhibitory effect of implementation example 2 wine Saccharomyces cerevisiae BY36 to apple blue mold and gray mold
[0027] 1. Experimental protocol
[0028] Take out Saccharomyces cerevisiae BY36 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 a single Colony into YPD liquid medium, culture at 26°C and 200r / min for 24h, centrifuge at 4000rpm for 5min, discard the supernatant, wash the collected bacteria repeatedly with sterile water for 3 times, count on a hemocytometer to prepare the concentration 1×10 8 cells / mL of Saccharomyces cerevisiae BY36 suspension.
[0029]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...
Embodiment 3
[0036] Implementation Example 3 The inhibitory effect of wine Saccharomyces cerevisiae BY36 on pear fruit botrytis
[0037] 1. Experimental protocol
[0038] Take out Saccharomyces cerevisiae BY36 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 a single Colony into YPD liquid medium, culture at 26°C and 200r / min for 24h, centrifuge at 4000rpm for 5min, discard the supernatant, wash the collected bacteria repeatedly with sterile water for 3 times, count on a hemocytometer to prepare the concentration 1×10 8 cells / mL of Saccharomyces cerevisiae BY36 suspension.
[0039] Activate 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 Botrytis cinerea spore suspension.
[0040] Healthy and unda...
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