Thelephora ganbajun Zang exopolysaccharide, preparation method thereof and application of exopolysaccharide
A technology of extracellular polysaccharide and dry bacteria cell, which is applied in the field of dry bacteria polysaccharide and can solve the problems of insufficient utilization and the like
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Embodiment 1
[0039] The acquisition of the strain of embodiment 1
[0040] 4 fresh dry fungus fruiting bodies were collected from different areas in Yunnan Province, and the surface was disinfected with 75% alcohol, and then rinsed with sterile water for several times. On the potato dextrose (PDA) medium plate, it was transferred to a 24 °C incubator for cultivation. After the hyphae grew, the purification was repeated until the pure culture of dry bacteria was obtained. Four dry bacteria strains were screened from the four dry bacteria fruiting bodies, and named TG-1, TG-2, TG-3, TG-4 respectively.
Embodiment 2
[0041] Example 2 Extraction of dry bacteria exopolysaccharide (EPS)
[0042]Carry out fermenter culture experiments, ① activation of strains. The dry bacteria TG-1, TG-2, TG-3 and TG-4 were inoculated on the activated medium plates (potato 200 g / L, glucose 20 g / L, magnesium sulfate 1 g / L, potassium dihydrogen phosphate 1.5 g / L) and cultured at 24 °C for 7 d. Take 0.5 cm 2 Dried bacteria activated strains were added to liquid medium (potato 200 g / L, glucose 20 g / L, peptone 2 g / L, magnesium sulfate 1 g / L, potassium dihydrogen phosphate 1.5 g / L), 500 mL triangular bottle The liquid volume was 300 mL, and then cultured with shaking at 24 °C for 10 d. ② Culture conditions. Loading volume: 7.5 liters; inoculation volume: 10%; fermentation temperature: 24°C; stirring speed: 350 r / min; foam control: add two drops of defoamer after inoculation. ③ Determination of pH value and DO value during fermentation. Use pH electrode and dissolved oxygen electrode to automatically measure an...
Embodiment 3
[0044] Example 3 In vitro antioxidant experiments
[0045] (1) Determination of reducing power
[0046] The reducing power was measured using the Prussian blue method. The exopolysaccharides of dry bacteria were diluted with deionized water in a gradient manner, and a series of polysaccharide aqueous solutions of different concentrations were prepared. Take 1 mL of polysaccharide sample into a test tube, add 2.5 mL of phosphate buffer (pH 6.6, 0.2 mol / L) and 1 mL of potassium ferricyanide solution (10 g / L), mix well and place it in a constant temperature water bath at 50 °C 20min. After the water bath, 2 mL of trichloroacetic acid (100 g / L) and 1.2 mL of ferric chloride solution (1 g / L) were added. After mixing, the absorbance at 700 nm was measured, and 2,6-di-tert-butyl-4-methylphenol (BHT) was used as a positive control.
[0047] (2) Determination of hydroxyl radical scavenging ability
[0048] The hydroxyl radical scavenging ability was determined by the Fenton method...
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