Zygosaccharomyces bayeri strain used for prevention and treatment of postharvest fruit diseases and its preparation method and application
A technology for Zygomyces zygosaccharomyces and fruit postharvest diseases, applied in the direction of microbial-based methods, biochemical equipment and methods, and preservation of fruits and vegetables, which can solve the lack of antibacterial spectrum strains, and the biocontrol effect has only been verified on a small number of fruits To achieve significant social and ecological benefits, avoid harm to people, and grow well
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Embodiment 1
[0019] Example 1: Biological properties of Zygosaccharomyces bailii strain BY39
[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 the reverse primer NL-4 (5'-GGTCCGTGTTTCAAGACGG-3') to PCR amplify the yeast 26S rDNA D1 / D2 region nucleic acid sequence, and PCR The sequencing results of the product were entered into the website www.NCBI.nlm.nih.gov for BLAST, the homologous sequences were downloaded from the GenBank...
Embodiment 2
[0026] The inhibitory effect of embodiment 2 Zygosaccharomyces Bayer BY39 on apple black spot
[0027] 1. Experimental protocol
[0028] Take Zygmus yeast BY39 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 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 Zygomyces Bayeris BY39 suspension.
[0029] Alternaria tenuissima was activated on a PDA medium plate, cultured at 26°C for 7-14 days, scraped an appropriate amount of spores, and prepared with sterile water to a concentration of 5×10 4 cells / mL of Alternaria spore suspension.
[0030] Healthy and undamaged apple fruits were steril...
Embodiment 3
[0033] Example 3 Inhibitory Effect of Zygosaccharomyces Bayer BY39 on Grape Postharvest Diseases
[0034] 1. Experimental protocol
[0035] Take Zygmus yeast BY39 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 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 Zyggiospermia BY39 suspension.
[0036] Activate Botrytis porri, Aspergillus aculeatus or Fusarium redolens on PDA medium plate, culture at 26°C for 7-14 days, scrape appropriate amount of spores, and prepare with sterile water into a concentration of 5 x 10 4 cells / mL of spore suspension of Botrytis cinerea, Aspergillus thornsp...
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