A gibberella strain and its application in the preparation of rutin and quercetin
A technology of Gibberella and quercetin, which is applied to a Gibberella strain and its application field in the preparation of rutin and quercetin, can solve the problems of insufficient resources of Sophora japonica, high cost, and many by-products of hydrolysis, and achieves The effect of protecting plant ecological diversity, short production cycle and low cost
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Embodiment 1
[0020] Embodiment 1, the separation and identification of Gibberella TG1
[0021] 1. Isolation of strains
[0022] The roots and rhizomes of Sinopodophyllum hexandrum (Royle) Ying collected from Xinglong Mountain (2300m above sea level) in Lanzhou City, Gansu Province were washed with tap water and placed in an ultra-clean workbench. Treat with 75% (volume percent) ethanol aqueous solution for 5 minutes, then rinse with sterile water for 3-5 times; then treat with 2.5% (mass percent) sodium hypochlorite aqueous solution for 10 minutes, and then rinse with sterile water for 3-5 times; Use sterilized tweezers and blades to peel off the outer skin of the root of Taoerqi, then cut into small pieces of 0.5cm×0.5cm and plant them on PDA solid medium, and cultivate them at 28°C for 3-7 days; at the same time, sterilize the same The roots of the treated Daoerqi were not peeled and cut, rolled on the PDA medium for one week, and cultured under the same conditions were observed as a co...
Embodiment 2
[0029] Embodiment 2, utilize Gibberella TG1 to prepare rutin and quercetin
[0030] 1. Cultivation of Gibberella TG1
[0031] The composition of the potato glucose liquid medium is: 200 g of peeled potatoes, 20 g of glucose, and add water to make the volume to 1000 mL. The preparation method of potato dextrose liquid medium: peel the potatoes and cut them into about 2cm 2 put into a beaker and boil for 30 minutes, then filter with double-layer gauze, take the filtrate and add glucose, then make up water, the pH is natural. Put 100ml of potato dextrose liquid medium in a 250ml Erlenmeyer flask, and sterilize it for later use.
[0032] A single colony of Gibberella TG1 was inoculated into 100ml of potato dextrose liquid medium, and cultured with shaking at 28°C and 120r / min for 7 days.
[0033] 2. Preparation of crude extract
[0034] 1. Take the fermentation system obtained in step 1, use a suction filter to separate and collect the fermentation supernatant.
[0035] 2. Ta...
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