Application of Bacillus megaterium YJB3 in plant growth promotion and bio-control
A Bacillus megaterium, plant growth-promoting technology, applied in plant growth regulators, plant growth regulators, botanical equipment and methods, etc., can solve problems such as soil ecological environment damage, agricultural product quality decline, soil environmental pollution, etc., to achieve Effects of reducing agricultural non-point source pollution, improving nutrient levels, and promoting plant growth
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Embodiment 1
[0030] The quantitative determination method of strain B. megaterium YJB3 phosphate-solubilizing ability refers to Liu et al. and their effects on plant growth and phosphorus mobilization in tropical soils. Biol. Fertile. Soils 50, 927-937.).
[0031] Ammonium molybdate hydrochloride solution: weigh 20g (NH 4 ) 6 MoO 24 4H 2 O was dissolved in 200mL of deionized water, stirred evenly and added to 425mL of concentrated hydrochloric acid, and then added to 50mL of deionized water after mixing.
[0032] Reducing agent: weigh 15g NaHSO 3 Dissolve in 250mL deionized water, mix well and add 1.5g Na 2 SO 4 and 0.5g of 1,2,4-aminonaphtholsulfonic acid, then dilute to 500mL, and store at 4°C in the dark for later use.
[0033] Phosphorus standard solution: weigh 0.10975g recrystallized KH 2 PO 4Dissolve in 0.1M HCl solution, and dilute to 500mL. The solution is 50 μg / mL phosphorus standard solution.
[0034] Drawing of phosphorus standard curve: draw phosphorus standard solu...
Embodiment 2
[0036] The strain B. megaterium YJB3 was inoculated on Ashby solid medium (nitrogen-free) (Kryuchkova, Y.V., Burygin, G.L., Gogoleva, et al., 2014. Isolation and characterization of aglyphosate-degrading rhizosphere strain, Enterobacter cloacae K7. Microbiol. Res. 169,99-105.), cultivated at 30°C for 3 days, observed its growth, and it was positive if there were colonies growing.
[0037] Nitrogenase activity was determined by acetylene reduction method in nmol C 2 h 4 / (h·mL) represents the activity of nitrogenase.
[0038]
[0039] Determination of nitrogenase activity of the strain YJB3 105.56 ~ 135.89nmol C 2 h 4 / (h·mL).
Embodiment 3
[0041] MM9 salt solution (g L -1 ): Na 2 HPO 4 60,KH 2 PO 4 3, NaCl 5, NH 4 Cl 10;
[0042] MKB (King's Medium L -1 ): K 2 HPO 4 2.5g, MgSO 4 ·7H 2 O 2.5g, acid hydrolyzed casein 5g, glycerin 13mL, pH 7.2.
[0043] CAS (chrome azure S) dye medium: take 2.7mg FeCl 3 ·6H 2 O was dissolved in 10mL of 10mM hydrochloric acid and added to 50mL of 1.21mg·mL -1 chrome azure solution, and then slowly pour this solution into 40mL1.82mg·mL -1 In the CTAB (cetyltrimethylammonium bromide) solution, stir continuously to avoid bubbles, forming a dark blue solution, and autoclave at 121°C for 20min. Add 30.24g Pipes (piperazine diethanolsulfonic acid) and 100mL MM9 salt solution to 750mL deionized water, adjust the pH of the solution to 6.8 with 50% NaOH, 15g agar, and autoclave at 121°C for 20min.
[0044] Quantitative determination of siderophilin production: inoculate the strain B. megaterium YJB3 in MKB liquid medium, culture at 30°C, 150rpm shaker for 3 days, centrifuge...
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