Endophyte and application thereof
A technology of plant endophytes and plants, applied in the direction of plant growth regulators, plant growth regulators, applications, etc., to achieve the effects of promoting absorption, improving soil physical and chemical properties, and efficient transformation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0032] The separation of embodiment 1 Sedum sedum endophytes
[0033] (1) culture medium
[0034] DF medium: every liter of culture medium contains KH 2 PO 4 4g, Na 2 HPO 4 6g, MgSO 4 ·7H 2 O0.2g, glucose 2g, sodium gluconate 2g, citric acid 2g, (NH 4 ) 2 SO 4 2 g, 0.1 mL each of component 1 and component 2 solutions, 15 g of agar, the solvent is water, pH 7.2, and sterilized by high pressure steam (121°C, 20 min).
[0035] Among them, component 1: H 3 BO 3 10mg, MnSO 4 ·H 2 O11.19mg, ZnSO 4 ·7H 2 O124.6mg, CuSO 4 ·5H 2 O78.22mg, MoO 3 Dissolve 10mg in 100mL sterilized distilled water and store at -4°C;
[0036] Component 2: FeSO 4 ·7H 2 O100mg was dissolved in 10mL sterilized distilled water and stored at -4°C.
[0037] DF+ACC medium: Add 3mM ACC to each liter of DF medium.
[0038] DF+ACC+Cd medium: add Cd to DF+ACC medium 2+ , the concentration is 0.5mM.
[0039] LB liquid medium: Each liter of culture medium contains tryptone 10g, yeast extract 5g, ...
Embodiment 2
[0044] The isolation and identification of embodiment 2 target bacterial strains
[0045] (1) culture medium
[0046] Enriched medium: KNO is contained in each liter of medium 3 10g, KCI1g, MgSO 4 ·7H 2 O0.5g, CaCl 2 1mg, FeSO 4 ·7H 2 O10mg, KH 2 PO 4 0.5g, 7.5g glucose, pH7.0, solvent is water, high pressure steam sterilization (121°C, 20min).
[0047] Separation medium: each liter of culture medium contains KN0 3 10g, KCI1g, MgSO 4 ·7H 2 O0.5g, CaCl 2 1mg, FeSO 4 ·7H 2 O10mg, KH 2 PO 4 0.5g, glucose 7.5g, agar 15.0g, pH7.0, solvent is water, high pressure steam sterilization (121°C, 20min).
[0048] Nitrate nitrogen conversion assay medium: each liter of culture medium contains KNO 3 1g, KCI1g, MgSO 4 ·7H 2 O0.5g, CaCl 2 1mg, FeSO 4 ·7H 2 O10mg, KH 2 PO 4 0.5g, 7.5g glucose, pH7.0, solvent is water, high pressure steam sterilization (121°C, 20min).
[0049] LB liquid medium: Each liter of culture medium contains tryptone 10g, yeast extract 5g, NaCl 1...
Embodiment 3
[0060] The identification of embodiment 3 target strain SAN1
[0061] (1) Observation of colony and cell morphology of SAN1 strain
[0062] Bacterial Morphological Study: Gram-stained bacteria were observed under an optical microscope with a 16×100 oil lens.
[0063] Research on the internal structure of the bacteria: Ultra-thin sections were made on the bacteria, and the internal structure of the bacteria was observed with a transmission electron microscope.
[0064] On solid medium, the young colonies of strain SAN1 were round, protruding, smooth and shiny, moist, translucent, viscous, and easy to pick. With the prolongation of culture time, the gloss of colony surface became darker and the color became light brown. Stained with basic fuchsin and observed under a microscope, most of the strains were blunt and round at both ends. Gram staining is positive, the bacteria are rod-shaped, the size is 2.5-3.3μm-1.3-2.1μm, producing spores, the spores are approximately columnar,...
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