Composite microbial agent and application thereof
A technology of compound microbial agent and microbial strain, which is applied in the field of microorganisms, can solve problems such as farmland soil compaction and hardening, social and economic losses, ecological safety and food safety, and achieve abundant and available microbial resources, stable phosphorus-dissolving function, and good promotion. the effect of the effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0042] A microbial inoculant comprising the following three strains:
[0043] Micrococcus luteus (Micrococcus luteus-GXMD-hs-11052), on August 12, 2021, with the preservation number GDMCC NO: 61867, was preserved in the Guangdong Microbial Culture Collection Center;
[0044] Bacillus subtilis (Bacillus subtilis-GXMD-hs-13035), with the preservation number GDMCC NO: 61868 on August 12, 2021, was preserved in the Guangdong Provincial Microbial Culture Collection Center;
[0045] Bacillus Paenibacillus Gxun-30, on June 13, 2019, with the preservation number GDMCC NO: 60687, was preserved in the Guangdong Microbial Culture Collection Center;
[0046] The composition by weight of the composite microbial bacterial agent is: 1-2 parts of Micrococcus luteus (Micrococcus luteus-GXMD-hs-11052), 1-2 parts of Bacillus subtilis (Bacillus subtilis-GXMD-hs-13035), fungoid 1-2 copies of Bacillus Paenibacillus Gxun-30. The ratio of the three strains is 1:1:1.
[0047] Application of the abo...
Embodiment 2
[0055] 1. Isolation, purification and identification of strains
[0056] Including the following steps:
[0057] Step 1 material preparation
[0058] Step 1.1 Sample sampling: The soil sampling site is Guangxi Nonggang National Nature Reserve. Remove the topsoil, collect soil samples at a depth of 15cm below the surface, store them in a 4°C incubator, and bring them back to the laboratory for further processing.
[0059] Step 1.2 Separation and purification medium:
[0060] LB liquid medium: tryptone 10.0g, yeast powder 5.0g, sodium chloride 5.0g, distilled water 1000mL.
[0061] LB solid medium: tryptone 10.0g, yeast powder 5.0g, sodium chloride 5.0g, agar powder 15g, distilled water 1000mL.
[0062] PDA medium: 200.0g potato, 20.0g glucose, 20.0g agar, 1000mL distilled water.
[0063] Step 2 Isolation and purification of bacterial strains
[0064] Step 2.1 Separation and Purification
[0065] Add 2g of soil sample to 18ml of sterile water to prepare soil suspension, sh...
experiment example 1
[0069] Single strain growth promotion experiment
[0070] 2.1 Preparation of strain fermentation broth
[0071] Streak the preserved strains on the LB solid medium, pick a single colony into 1ml LB liquid medium for shaking culture overnight, inoculate 1ml of the above bacterial solution into the liquid medium, shake the table (30-32°C, 150-200r / min) After one day of shaking culture, it was used to water the experimental seedlings.
[0072] 2.2 Seedling growth promotion experiment
[0073] Use the seedlings of Citrus aurantii to carry out the experiment, and the specific steps are as follows:
[0074] Slow seedlings: transplant the experimental seedlings of Fructus Aurantii into flower pots filled with soil + substrate (1:1) to ensure that the nutrition of the original soil is relatively consistent.
[0075] Seedling selection: After slowing down the seedlings for a period of time, pick the Fructus aurantii seedlings with relatively consistent growth to carry out the exper...
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