Rice bacterial brown streak germ phage and application thereof
A brown streak pathogen, bacterial technology, applied in the field of rice bacterial brown streak pathogen phage, can solve the problem of no phage, etc., and achieve a strong cracking effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0029] Example 1 Isolation of Rice Bacterial Brown Streak Phage
[0030] (1) Isolation of rice bacterial brown streak pathogen
[0031] ① After soaking and grinding the rice disease species, let it stand for a period of time, take the supernatant for gradient dilution and spread on the plate, and place the plate upside down in a 30°C incubator for cultivation;
[0032] ② After culturing for 48 hours, a single colony of suspected rice bacterial brown streak pathogen was picked and purified;
[0033] ③The isolated strains were tested for tobacco allergy and rice pathogenicity, and the strains that were all positive were taken, and the genomic DNA was extracted for 16S rDNA sequencing (see SEQ ID No.1 for the sequencing results).
[0034] Thus, a rice bacterial brown streak pathogen (Aaa RS-2) was isolated and verified, and the bacteriophage was isolated using this strain as a host bacterium.
[0035] (2) Isolation of rice bacterial brown streak pathogen phage
[0036] ① Soak ...
Embodiment 2
[0040] Example 2 Determination of biological properties of rice bacterial brown streak pathogen phage
[0041] (1) Determination of phage titer
[0042] After the last purification, evenly distributed and uniformly sized phage plaques were obtained. Prick a single phage plaque with a tip and soak the tip in 1ml of SM liquid medium at 4°C overnight. Take 0.1 phage plaque the next day. Inoculate 5ml of LB liquid medium with 0.1ml of supernatant and 0.1ml of host bacteria solution, incubate at 30°C for 6 hours, then centrifuge and filter, make 10-fold gradient dilution with SM solution, and finally dilute to 10 -8 , absorb 0.1ml of the last three dilutions of phage dilution and mix with 0.1ml of host bacteria, incubate at 30°C for 20min and spread double-layer agar plates. Observe the number of plaques and calculate the phage titer according to the following formula:
[0043] Phage titer = number of plaques × dilution factor / sampling volume;
[0044] Three parallel samples a...
Embodiment 3
[0051] Example 3 Bacteriophages are used to control rice bacterial brown streak disease
[0052] (1) Under in vitro conditions, the lysis curve of phages against the rice bacterial brown streak pathogen
[0053] The host bacterium Aaa RS-2 was cultivated to the pre-logarithmic phase, and 2ml of the culture was added to 5ml of LB liquid medium; among them, 20μl of phage (2×10 7 pfu / ml), the control group was added with 20 μl LB liquid medium, and cultured in a shaker. Samples were taken at each time point in a 96-well plate for OD value determination, and the lysis curve was drawn. The lysis curve was as follows: Figure 4 .
[0054] Such as Figure 4 As shown, the rice bacterial brown streak pathogen phage significantly reduces the number and growth rate of host bacteria, and can be used to prevent and control rice bacterial brown streak pathogen.
[0055] (2) Control effect of phage on rice bacterial brown streak disease under living conditions
[0056] Soak the seeds in...
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