Growth promotion endophytes for astragalus membranaceus and growth promotion method and application thereof
An endophyte, astragalus technology, applied in the directions of microorganism-based methods, biochemical equipment and methods, plant growth regulators, etc., to achieve the effect of good acid resistance activity
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Embodiment 1
[0016] Example 1: Determination of the volatile components of the main green leaves of Astragalus membranaceus
[0017] The 2, 5, and 7-year-old fresh Astragalus membranaceus from Hunyuan, Shanxi Province were used as materials, and aseptically separated into periderm, secondary phloem, and secondary xylem. After grinding with liquid nitrogen, 0.2 g samples were taken, and headspace GC-MS was used to analyze its Volatile Spectrum. With n-hexanal, E - 2 -Hexenal and n-hexanol were used as reference substances, and the relevant substances in the samples were identified according to their representative ion fragments and retention time. According to the peak areas of the three in the sample, calculate their relative content. GraphPad Prism (5.01) was used for data processing and significant difference analysis, and the threshold was set at P<0.05.
[0018] For a representative total ion current chromatogram see figure 1 . It can be seen from the figure that different anato...
Embodiment 2
[0023] Example 2: Determination of endophytic strains containing ACC deaminase and other life-promoting activities in Radix Astragali
[0024] The 5-year-old fresh roots of Astragalus membranaceus in Hunyuan, Shanxi Province were used as materials, and the endophytic bacteria of Astragalus membranaceus were isolated by tissue block separation method. The specific operation is as follows: wash the harvested fresh Astragalus membranaceus several times with tap water, wash away the soil remaining on the root surface, and then rinse it with sterile water containing 10% Tween-20; Cut into 1 cm long sections, soak in 75% alcohol for 1 min, rinse with sterile water for 3 times, soak in 5% NaClO for 10 min, rinse with sterile water for 3 times, then rinse with 75% alcohol for 40 s , rinsed with sterile water 5 times, absorbed excess water with sterile filter paper, put the treated material in a sterile mortar, added 2 mL of normal saline, mashed, and ground.
[0025] Take 100 μL of s...
Embodiment 3
[0050] Example 3: Determination of n-hexanal growth-promoting bacterial strain and its concentration range
[0051] With 50% ethanol as solvent, prepare 2, 10, 50, 250, 1250, 6250 mM E-2 - The hexenal stock solution is added to the LB liquid medium according to the addition amount of 1‰ volume. 1‰ of the inoculum, the above strains were inoculated with different concentrations of E-2 - LB medium of hexenal, cultured on a shaker at 28°C until logarithmic growth phase, and measured OD600. Those who added the same volume of sterile water and 50% ethanol were used as blank control and solvent control respectively. Three biological replicates were set up for each concentration.
[0052] Taking the average value of OD600 of the blank control as a reference, calculate E-2 - Effect of hexenal addition on strain growth. the result shows, E-2 -Hexenal has the effect of promoting the growth of Sphingobacterium strain KSC01, see image 3 .
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