Bjerkandera sp. Gause 15 for controlling vegetable root diseases and preparation thereof
A technology for root diseases and tobacco pipe bacteria, applied in the direction of fungicides, biocides, fungi, etc., to achieve good development and application prospects, easy industrial production, and low pollution effects
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0039] Embodiment 1: the preparation of Gao's No. 15 bacterial strain fermented liquid
[0040] (1) Medium:
[0041] Gore's medium: 1 g KNO 3 , 0.5 g K 2 HPO 4 , 0.5 g MgSO 4 ·7H 2 O, 0.5 g NaCl, 0.01 g FeSO 4 ·7H 2 O, 20g agar or 13g agar powder, pH=7.4-7.6, 1000ml water.
[0042] (2) Strain culture:
[0043] Scrape a small amount of bacterial liquid from the surface of the preserved strains, streak on the Gowell medium plate, incubate at 30°C for 24 hours, pick a single colony into 2 ml of Gowell medium, 200 rpm, and incubate at 30°C for 24 hours , and then inserted into a 250-mL Erlenmeyer flask with a medium filling volume of 80 mL at a ratio of 10%, cultured at 30° C. for 48 hours at 200 rpm.
[0044] (3) Expand fermentation:
[0045] Inoculate the strain solution in a 50-liter fermenter with a 0.5% inoculation ratio, and feed 35 liters of fermentation culture material in a 50-liter fully automatic fermenter. The fermentation conditions are: temperature 30°C, 12...
Embodiment 2
[0046] Embodiment 2: strain identification and preservation
[0047] 2.1 Morphological characteristics
[0048] Morphological identification: Streak the Gaoshi No. 15 strain on the Gaoshi medium plate, and observe the morphology after culturing at 30°C for 48 hours. After 48 hours of shaking culture in Gaoke's liquid medium, the shape, size, spore formation and flagella growth mode of the bacteria were observed.
[0049] Observation results: Opaque milky white radial colonies are formed on Gore's medium, the surface is thin and unevenly distributed. The mycelium is thin, short and easy to break.
[0050] 2.2 Identification and preservation
[0051] Molecular identification: The DNA gene of Gaoshi 15 was sequenced by Wuhan Aoke Dingsheng Biotechnology Co., Ltd. The sequencing primer was: ITS1, and a gene fragment with a length of 266bp was obtained.
[0052] Comparison of the gene sequence with the published gene sequence on the NCBI website (www.ncbi..nlm.nih) shows that t...
Embodiment 3
[0056] Embodiment 3: the preparation process of Gaoshi No. 15 wettable powder inoculum
[0057] The fermented fermented body is processed into wettable powder according to the following method: firstly carry out the archaic fermentation culture of the thalline (same as expanded fermentation). Then filter through plate frame, dry and pulverize to make wettable powder. The specific production process is as follows:
[0058] Plate and frame filtration: Press the material from the storage tank into the plate and frame with a pressure of 10 kg / cm2, and filter through No. 3 gauze. The pressure should be adjusted at any time so that the content of bacteria in the bacteria does not exceed 20 million / ml.
[0059] Drying: Ventilate and dry in a drying room with a temperature below 60°C to a moisture content of 5-8%.
[0060] Pulverization: The output temperature should not exceed 70°C during pulverization to prevent the inactivation of bacteria.
[0061] Determination of finished pro...
PUM
Property | Measurement | Unit |
---|---|---|
diameter | aaaaa | aaaaa |
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