Mucor for producing picropodophyllin and its glucoside and kaempferol flavone kind substance, its method and application
A technology of kaempferol flavonoids and podophyllotoxin, which is applied in the field of microorganisms, can solve problems such as increased demand, destruction of plant resources, loss of biodiversity and ecological environment, etc., achieves short production cycle, simple nutritional requirements, and protection of plant ecology The effect of diversity
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Embodiment 1
[0044] The Taoerqi plant was collected from Taibai Mountain, and the pure strain GJ-TW8 was isolated, purified and screened out by tissue separation method and preserved for future use.
[0045] PDA medium: 100ml of 20% potato juice, 2g of sucrose, pH 6.5. Add 2g of agar to the seed medium; the fermentation medium is liquid.
[0046]The GJ-TW8 bacterial strain provided by the present invention is connected to the seed medium, cultivated for 5 days at 28°C, transferred to a 500ml Erlenmeyer flask with 200ml of fermentation medium, 29°C, 180r / min, and shakes the flask for 7 days. Collect 40L of the fermentation culture, filter with suction, collect about 4250g of wet mycelium, take it out after freezing for 4 hours, break the mycelium, and extract the broken mycelium with equal volumes of chloroform and n-butanol in turn. The chloroform extract and the n-butanol extract were collected respectively, and concentrated under reduced pressure at 60°C to 10 ml.
[0047] The concentr...
Embodiment 2
[0050] ISP fermentation medium: soluble starch 10g, K 2 HPO 4 1.0g, MgSO 4 1.0g, NaCl 1.0g, (NH 4 ) 2 SO 4 2.0g, trace element solution 1ml, distilled water 1000ml, pH6.8 (trace element solution: FeSO 4 ·7H 2 O 0.1g, MnCl 2 4H 2 O 0.1g, ZnSO 4 ·7H 2 O 0.1g, distilled water 100ml)
[0051] The GJ-TW8 bacterial strain provided by the present invention is inoculated in PDA seed culture medium 28 ℃, after cultivating 5 days, transfers in the 500ml Erlenmeyer flask that 200ml ISP fermentation medium is housed, 29 ℃, 180r / min, shaking flask culture 7 days, Collect 3160 g of wet mycelium, freeze for 4 hours, break the mycelium, and extract the broken mycelium with equal volumes of chloroform and n-butanol respectively. The chloroform extract and the n-butanol extract were collected respectively, and concentrated under reduced pressure at 60°C to 10 ml.
[0052] The concentrated chloroform extract was separated by silica gel column chromatography (silica gel 200-300 mes...
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