Method for extracting flavone from kudzuvine root fermentation butyl alcohol and residue thereof
A technology for fermenting butanol and residues, which is applied in the field of utilization of kudzu resources, can solve the problems of difficult industrialization of kudzu resources, lack of comprehensive utilization of raw materials, etc.
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Embodiment 1
[0023] Example 1: Get 50g of kudzu root (wherein the kudzu root starch content is 56%), add 200mL of distilled water, adjust to pH 6.5 with NaOH, sterilize at 121°C for 20min, then add 800mL of sterilized yeast powder containing 6g / L, 2.938 g / L K 2 HPO 4 and 1.768g / L KH 2 PO 4 Add 5% (v / v) seed solution to the culture solution, and anaerobically cultivate it at 37°C for 3 days; separate the culture medium from solid-liquid to obtain fermentation broth and fermentation residue, and use gas chromatography to measure the total solvent content in the fermentation broth. Butanol content is 4.47g / L; Acetone content is 2.16g / L; Weigh 2g of fermented residue (dry weight), extract and reflux 3 times at 80°C with 30ml of 80% ethanol, 2 hours each time; the extraction amount of flavonoids measured was 3.012g / 100g of kudzu root dry material, which was 12% higher than the extraction amount of flavonoids directly extracted from kudzu root.
Embodiment 2
[0024] Embodiment 2: Get Pueraria 100g (wherein Pueraria starch content is 56%), add 200mL distilled water, adjust to pH6.5 with NaOH, sterilize at 121 ℃ for 20min, then add 800mL sterilized containing 6g / L peptone, 2.938 g / LK 2 HPO 4 and 1.768g / LKH 2 PO 4 Add 5% (v / v) seed solution to the culture solution, and anaerobically cultivate it for 4 days at 37°C; separate the culture medium from solid-liquid to obtain fermentation broth and fermentation residue, and measure the total amount of solvent in the fermentation broth by gas chromatography It is 13.23g / L; Butanol content is 8.69g / L; Acetone content is 3.76g / L; Take 2g fermented residue (dry weight), use the ethanol of 30ml of 80% to extract and reflux 3 times at 80 ℃, every Second 2h; The extraction amount of flavonoids measured was 2.965g / 100g of kudzu root dry material, which was 11.8% higher than the extraction amount of flavonoids directly extracted from kudzu root.
Embodiment 3
[0025] Example 3: Get 140g of kudzu root (wherein the kudzu root starch content is 56%), add 200mL of distilled water, adjust to pH6.0 with NaOH, sterilize at 121°C for 20min, then add 800mL of sterilized solution containing 4.3g / L ammonium acetate , 2.938g / L K 2 HPO 4 and 1.768g / L KH 2 PO 4Add 10% (v / v) of the seed liquid to the culture solution, and anaerobically cultivate it for 4 days at 37°C; separate the culture medium from solid-liquid to obtain the fermentation liquid and fermentation residue, and measure the total amount of solvent in the fermentation liquid by gas chromatography It is 21.16g / L; Butanol content is 13.28g / L; Acetone content is 6.53g / L; Take by weighing 2g fermented residue (dry weight), use the ethanol of 30ml of 80% to extract and reflux 3 times at 80 ℃, every Second 2h; The extraction amount of flavonoids measured is 2.950g / 100g of kudzu root dry material, which is 11.7% higher than the extraction amount of flavonoids directly extracted from kudzu...
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