Cherry preservative and fresh-keeping microbial preparation and preparation method and application thereof
A technology for microbial preparations and microbial strains is applied in the field of plant disease prevention and control, and can solve problems such as sweet cherries and differences in antibacterial spectrum that have not yet been consulted.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0044] Embodiment 1, isolation and identification of pathogenic bacteria and verification of pathogenicity
[0045] 1.1 Isolation and identification of pathogenic bacteria
[0046] Carry out surface disinfection with 75% medical alcohol of rotten sweet cherry sample, then wash the surface 3 times with sterile water, air-dry naturally, cut a small amount of rotten fruit tissue with sterile blade and tweezers, place it in resistant (streptomycin , penicillin) in the middle of the PDA medium, and cultivated at a constant temperature of 28°C for 3-4d. After the plate colony grows, pick the edge bacterial block and place it in another PDA medium, cultivate it at a constant temperature of 28°C, and purify it several times until a single colony is reached. A single colony was inoculated on the slant of the test tube and stored in a 4°C refrigerator for later use. All the above operations were carried out in a sterile environment.
[0047] The isolated and purified pathogenic bacte...
Embodiment 2
[0057] Embodiment 2, separation, screening and identification of antagonistic bacteria
[0058] 2.1 Isolation and screening of endogenous antagonistic bacteria
[0059] Take 30 healthy "Meizao" sweet cherry whole fruits and grind them, weigh 1g of the pulp and add it to 9mL sterile saline, mix well to make a stock solution, and let it stand for 20 minutes. Using serial dilution method, dilute to 10 -3 、10 -4 、10 -5 Take 100 μL of the dilution solution of the above concentration and spread it on LB solid medium, set 3 parallels for each gradient, and incubate at a constant temperature of 37°C for 24h. The grown colony was inoculated onto another LB solid medium for three-section line, and incubated at a constant temperature of 37°C until a single colony grew. Pick a single colony to the LB slant, and store it at 4°C after the colony grows.
[0060] Using the filter paper method, take a 6mm bacterial cake on a PDA plate where the pathogenic bacteria Rhizopus stoloniferum wa...
Embodiment 3
[0072] Embodiment 3, the influence of endophytic antagonistic bacteria different treatment solutions on the growth of pathogenic bacteria
[0073] Bacillus Velez Q-84 was cultured and prepared into different treatment liquids, (A) fermentation broth: inoculated Bacillus Velez Q-84 in NB liquid medium and fermented at 37°C and 180r / min for 96h; (B ) Bacterial suspension: inoculate Bacillus Velez Q-84 in NB liquid medium, ferment at 37°C and 180r / min for 96h, centrifuge at 6000g for 10min, discard the supernatant, add the same volume of sterile water and shake well; (C) Supernatant: inoculate Bacillus Velez Q-84 in NB liquid medium, ferment and culture at 37°C, 180r / min for 96h, centrifuge at 6000g for 10min, take the supernatant, and pass through a 0.22μm filter membrane; (D ) Control: NB liquid medium. Adopt filter paper sheet method, method is with 2.1 in the embodiment 2, observes the influence of different treatment liquids on the inhibitory effect of rhizopus stolonifer, ...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com