Saccharomyces cerevisiae BY21 for preventing and controlling postharvest diseases of fruits and vegetables, and preparation method and using method of saccharomyces cerevisiae BY21
A technology of Saccharomyces cerevisiae and BY21, which is applied in the field of Saccharomyces cerevisiae for biological control of postharvest diseases of fruits and vegetables, can solve the problems that the biocontrol effect is only verified on a small number of fruits, lack of strains with antibacterial spectrum, etc., and achieve significant social and ecological benefits, Stable properties and high safety effects
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Embodiment 1
[0017] Example 1: Biological properties of Saccharomyces cerevisiae BY21
[0018] 1. Morphological features
[0019] (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.
[0020] (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.
[0021] 2. Molecular biological identification
[0022] The nucleic acid sequence of the Saccharomyces cerevisiae BY21 26S rDNA D1 / D2 region was amplified by PCR with the universal forward primer NL-1 (5'-GCATATCAATAAGCGGAGGAAAAG-3') and the reverse primer NL-4 (5'-GGTCCGTGTTTCAAGACGG-3'). The sequencing results of the PCR products were entered into the website www.NCBI.nlm.nih.gov for BLAST, the homologous sequences were...
Embodiment 2
[0024] The inhibitory effect of implementation example 2 Saccharomyces cerevisiae BY21 on pear fruit blue mold
[0025] 1. Experimental protocol
[0026] Take Saccharomyces cerevisiae BY21 out of 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 Put it into YPD liquid medium, cultivate it under the conditions of 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 the hemocytometer and prepare a concentration of 1×10 8 cells / mL of Saccharomyces cerevisiae BY21 suspension.
[0027] Activate Penicillium expansum 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 spore suspensi...
Embodiment 3
[0031] Implementation example 3 Saccharomyces cerevisiae BY21 is to the inhibitory effect of grape postharvest disease
[0032] 1. Experimental protocol
[0033] Take Saccharomyces cerevisiae BY21 out of 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 Put it into YPD liquid medium, cultivate it under the conditions of 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 the hemocytometer and prepare a concentration of 1×10 8 cells / mL of Saccharomyces cerevisiae BY21 suspension.
[0034] Botrytis porri, Aspergillus aculeatus, Alternaria eichhorniae, Fusarium redolens, Colletotrichum fructicola or Trichothecium roseum ) was activated on a PDA medium plate, cultured at 26°C for 7-14 days, scrape...
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