Bacteria d10 for improving the effectiveness of heavy metals and its application
A heavy metal and effective technology, applied in the fields of agricultural technology and environmental pollution control applications, can solve the problem of small total biomass, and achieve the effect of promoting plant growth and increasing the content of heavy metals in plants
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0039] The heavy metal-resistant plant growth-promoting bacteria D10 strain of the present invention is isolated and purified from the root nodules of alfalfa (Medicogo sativa L.) grown in heavy metal-contaminated soil, and the separation and identification method is as follows:
[0040] Gently pull the alfalfa from the soil, shake off the roots to loosen the soil and rinse with water. Select the plump, large-diameter pink nodules on the taproot and cut them off with scissors. Soak the cut nodules in deionized water for 4-5 minutes to remove the remaining impurities, soak and disinfect with 75% ethanol for 2-3 minutes, wash with water 2-3 times, soak in 3% NaClO solution for 5 minutes, and finally use sterile deionized Wash with water 5-7 times. Under sterile operating conditions, put the surface-sterilized nodules into YMA solid plates containing 0.3% Congo red [mannitol 10.0 g, yeast powder 1.0 g, MgSO 4 ·7H 2 O 0.2g, K 2 HPO 4 0.5g, NaCl 0.1g, anhydrous CaCl 2 0.05g,...
Embodiment 2
[0042] Example 2 Activation of strain D10 and preparation of bacterial suspension
[0043] The D10 (CCTCC NO: M 2016554) slant strain was inoculated into TY solid medium (tryptone 5.0 g, yeast extract 3.0 g, CaCl 2 0.3g, agar 20g, distilled water 1000ml, pH 7.0), cultured at 30°C for 3 days. Then select plump and viscous D10 colonies to inoculate in TY liquid medium (tryptone 5.0g, yeast extract 3.0g, CaCl 2 0.3g, distilled water 1000ml, pH 7.0), shaking at 150rpm at 30°C for 20-24h, so that the number of cells reaches more than 500 million CFU / ml.
Embodiment 3
[0044] Example 3 The ability of strain D10 to produce IAA
[0045] According to the determination method of Gordon and Weber (1951), TY liquid medium was divided into test tubes, each tube was 4 mL, and 1 mL of filter-sterilized 2.5 mg / mL tryptophan solution was added after high-temperature sterilization at 121 °C to make the medium in color. The final concentration of amino acid was 0.5 mg / mL. D10 (CCTCC NO: M 2016554) was inoculated into the above-mentioned medium and cultured with shaking at 30°C for 3 days. The fermentation broth was centrifuged at 12000 r / min for 5 min, 1 mL of the supernatant was taken, 50 μL of 10 mM orthophosphoric acid was added, and 2 mL of Sackowski's chromogenic reagent was added. Sterile medium was treated the same as above and zeroed as a control. The concentration of IAA in the fermentation broth was calculated by using IAA standard solution with concentrations of 0, 5, 10, 20, 40, and 60 mg / L as a standard curve in the same way. The results ...
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