Preparation method and application of fermentation products of edible and medical fungus
A technology of fermentation products and edible and medicinal bacteria, applied in the direction of microorganism-based methods, biochemical equipment and methods, applications, etc., to achieve the effect of optimizing fermentation methods and increasing content
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[0046] Annexin preparation:
[0047] Put the sulphurite into liquid nitrogen, take it out after 10min-15min for crushing, put the crushed tissue in Tris-HCl buffer containing 5mmol / L EDTA (Tris-HCl buffer pH7.4, concentration 10mmol / L ), homogenate for 3 minutes, then centrifuge the homogenate at 4°C and 8000rmp for 20 minutes, discard the precipitate, and freeze-dry the supernatant into a freeze-dried powder; dissolve the freeze-dried powder in 0.05mol / LTris-HCl buffer , placed in a dialysis bag with a molecular weight exclusion value of 6kDa, and dialyzed against 0.05mol / LTris-HCl buffer solution at 4°C overnight; after the dialyzed sample was centrifuged to remove the precipitate, it was loaded on a well-balanced DEAECellulose DE-52 anion exchange column , use 0.05mol / L Tris-HCl buffer to pass through the column, the flow rate is 0.4mL / min, 6mL per tube is automatically collected, and the corresponding sample components are detected and collected at ultraviolet 280nm. After...
Embodiment 1
[0049] 1. Material preparation
[0050] PDA plate medium: potato 200g, glucose 20g and agar 15g, dilute to 1000ml with water, natural pH, sterilize at 121°C for 20min.
[0051] Inoculate the Rhodotrametes strains preserved on the slant onto the PDA plate culture medium and activate and cultivate them at 22° C. for 10 days to obtain the activated Rhodotramets strains.
[0052] Liquid seed medium: glucose 12g, yeast powder 4g, peptone 3g, KH 2 PO 4 1g and MgSO 4 0.5g, dilute to 1000mL with water, keep the pH natural, and sterilize at 121°C for 20min.
[0053] The solid medium is composed of the following mass percentage components: K 2 HPO 4 0.1%, MgSO 4 0.1% and the rest of water, with natural pH, sterilized at 121°C for 20min.
[0054] The composition of the liquid fermentation medium is: based on 1L liquid fermentation medium, glucose 25g, peptone 6g, yeast powder 5g, KH 2 PO 4 1.0g, MgSO 4 0.5g and the rest of water, with natural pH, sterilized at 121°C for 20m...
Embodiment 2
[0076] 1. Material preparation
[0077] PDA plate medium: potato 200g, glucose 20g and agar 20g, dilute to 1000ml with water, natural pH, sterilize at 121°C for 20min.
[0078] Inoculate the rhizome strains preserved on the slant on the PDA plate culture medium and activate and culture them at 30° C. for 3 days to obtain the activated rhizome strains.
[0079] Liquid seed medium: glucose 5g, yeast powder 4g, peptone 3g, KH 2 PO 4 1g and MgSO 4 0.5g, dilute to 1000mL with water, keep the pH natural, and sterilize at 121°C for 20min.
[0080] The solid medium is composed of the following mass percentage components: K 2 HPO 4 0.2%, MgSO 4 0.05% and the rest of water, with natural pH, sterilized at 121°C for 20min.
[0081] The liquid fermentation medium is the same as in Example 1.
[0082] 2. Preparation of medicinal bacteria fermentation products:
[0083] (1) Preparation of liquid seed solution of Rhodotrametes: Dilute 1cm 2 Inoculate the bacterium blocks of rhiz...
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